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Paclitaxel Treatment Options in United Kingdom
A collection of 293 research studies where Paclitaxel is the interventional treatment. These studies are located in the United Kingdom . Paclitaxel is used for conditions such as Breast Cancer, Ovarian Cancer and Non-Small Cell Lung Cancer.
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A Phase 2 Study of MM-141 Plus Nab-paclitaxel and Gemcitabine in Front-line Metastatic Pancreatic Cancer
Completed
The purpose of this study is to determine whether the combination of MM-141 plus nab-paclitaxel and gemcitabine is more effective than nab-paclitaxel and gemcitabine alone based on Progression Free Survival (PFS) in front-line metastatic pancreatic cancer patients with high serum levels of free IGF-1.
The purpose of this study is to determine whether the combination of MM-141 plus nab-paclitaxel and gemcitabine is more effective than nab-paclitaxel and gemcitabine alone based on Progression Free Survival (PFS) in front-line metastatic pancreatic cancer patients with high serum levels of free IGF-1. Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
09/17/2018
Locations: Banner MD Anderson Cancer Ctr., Gilbert, Arizona +65 locations
Banner MD Anderson Cancer Ctr., Gilbert, Arizona
Pacific Cancer Medical Center, Inc., Anaheim, California
St. Jude Heritage Healthcare, Fullerton, California
UCLA School of Medicine, Los Angeles, California
Cancer Care Assoc Med Grp, Redondo Beach, California
UCSF Cancer Center, San Francisco, California
Sansum Clinic, Santa Barbara, California
Central Coast Med Onc Corp, Santa Maria, California
Rocky Mountain Cancer Centers, Aurora, Colorado
Baptist Health Med Gr Onc, LLC, Miami, Florida
Florida Cancer AffiliatesOcala, Ocala, Florida
Memorial Regional Hospital, Pembroke Pines, Florida
Cancer Treatment Centers of America-Georgia, Newnan, Georgia
Northwestern University, Chicago, Illinois
University of Illinois at Chicago, Chicago, Illinois
Illinois Cancer Specialists, Chicago, Illinois
Oncology Specialists, S.C., Park Ridge, Illinois
Midwest Regional Medical Cntr, Zion, Illinois
Nylen Cancer Center, Sioux City, Iowa
Cancer Center of Acadiana Research Department, Lafayette, Louisiana
Reliant Medical Group, Inc., Worcester, Massachusetts
Compr Cancer Centers of Nevada, Henderson, Nevada
New York Oncology HematologyPC, Albany, New York
Roswell Park Cancer Inst, Buffalo, New York
Bassett Cancer Institute, Cooperstown, New York
North Shore Hematology Oncology Associates, PC, East Setauket, New York
Columbia University Medical Center, New York, New York
Columbia University, New York, New York
Mid Ohio Onco/ Zangmeister Ctr, Columbus, Ohio
Tulsa Cancer Institute, PLLC, Tulsa, Oklahoma
St. Luke's University Health Network, Bethlehem, Pennsylvania
Fox Chase Cancer Center, Philadelphia, Pennsylvania
Allegheny Cancer Center, Pittsburgh, Pennsylvania
Vanderbilt-Ingram Cancer Ctr, Nashville, Tennessee
SCRI - Tennessee Oncology, Nashville, Tennessee
Texas Oncology-Austin Midtown, Austin, Texas
Texas Oncology P A Bedford, Bedford, Texas
Texas Oncology-Dallas P.H., Dallas, Texas
Brooke Army Medical Center (BAMC), Fort Sam Houston, Texas
Texas Oncology-Paris, Paris, Texas
Texas Oncology-Plano East, Plano, Texas
Texas Oncology SA Medical Ctr, San Antonio, Texas
Texas Oncology-Tyler, Tyler, Texas
Virginia Cancer Specialists PC, Fairfax, Virginia
Onc and Hem Asso of SW VA Inc, Salem, Virginia
Cancer Care Northwest, P.S., Spokane Valley, Washington
Northwest Cancer SpecialistsPC, Vancouver, Washington
Cross Cancer Institute, Edmonton, Alberta
Klinikum rechts der Isar - TUM, Munchen, Bayern
Universitaetsklinikum Koeln, Koeln, Nordrhein Westfalen
Caritasklinik St. Theresia, Saarbruecken, Saarland
Vivantes Klinikum Neukoelln, Berlin, Not set
Charite Universitaetsmd Berlin, Berlin, Not set
Uniwersyteckie Centrum Kliniczne, Gdansk, Not set
WSZ im. L. Rydygiera wToruniu, Torun, Not set
Hospital Universitario Marques de Valdecilla, Santander, Cantabria
Hospital Universitari Vall d'Hebron, Barcelona, Not set
Hospital General Universitario Gregorio Marañon, Madrid, Not set
Centro Integral Oncologico Clara Campal, Madrid, Not set
Hospital U de Fuenlabrada, Madrid, Not set
Hospital Clinico Universitario de Valencia, Valencia, Not set
Guy's Hospital, London, Greater London
Sarah Cannon Research Institute UK, London, Greater London
The Christie, Manchester, Greater Manchester
Royal Marsden Hospital, Sutton, Surrey
Royal Marsden Hospital, Sutton, Not set
Conditions: Pancreatic Cancer
Study Evaluating Neratinib Plus Paclitaxel VS Trastuzumab Plus Paclitaxel In ErbB-2 Positive Advanced Breast Cancer
Completed
This study is investigating the effects of an experimental drug (neratinib) in combination with paclitaxel versus trastuzumab in combination with paclitaxel for the treatment of women who have not received previous treatment for erbB-2-positive locally recurrent or metastatic breast cancer. The study will compare the effectiveness of each regimen in shrinking tumors and extending the lives of women with erbB-2 (HER2) positive breast cancer. The study will also compare the safety of the two regim... Read More
This study is investigating the effects of an experimental drug (neratinib) in combination with paclitaxel versus trastuzumab in combination with paclitaxel for the treatment of women who have not received previous treatment for erbB-2-positive locally recurrent or metastatic breast cancer. The study will compare the effectiveness of each regimen in shrinking tumors and extending the lives of women with erbB-2 (HER2) positive breast cancer. The study will also compare the safety of the two regimens and as well as the quality of life of subjects receiving either regimen. Read Less
Gender:
FEMALE
Ages:
18 years and above
Trial Updated:
07/25/2018
Locations: Ventura County Hematology-Oncology Specialists, Oxnard, California +194 locations
Ventura County Hematology-Oncology Specialists, Oxnard, California
Redwood Regional Medical Group, Santa Rosa, California
Cancer Center of Central Connecticut, Plainville, Connecticut
Palm Beach Institute of Hematology and Oncology, Boynton Beach, Florida
North Broward Medical Center Cancer Center, Deerfield Beach, Florida
Broward General Medical Center, Fort Lauderdale, Florida
Mid Florida Cancer Centers, Orange City, Florida
Florida Cancer Research Institute, Plantation, Florida
Hematology Oncology Associates of Treasure Coast, Port Saint Lucie, Florida
Phoebe Cancer Center, Albany, Georgia
Dublin Hematology and Oncology Care, Dublin, Georgia
Clintell, Skokie, Illinois
Presence Hematology and Oncology, Skokie, Illinois
Springfield Clinic, Springfield, Illinois
CHRISTUS St. Frances Cabrini Hospital, Alexandria, Louisiana
Hematology Oncology Services, Metairie, Louisiana
Park Nicollet Institute, Saint Louis Park, Minnesota
Missouri Cancer Associates, Columbia, Missouri
Washington University School of Medicine Siteman Cancer Center, Saint Louis, Missouri
St. John's Medical Research Institute, Springfield, Missouri
The Valley Hospital, Luckow Pavilion Office of Oncology Clinical Trials, Paramus, New Jersey
Gaston Hematology and Oncology Associates, Gastonia, North Carolina
Summa Health System Hospitals, Akron, Ohio
Warren Cancer Research Foundation, Tulsa, Oklahoma
Samaritan Hematology and Oncology Consultants, Corvallis, Oregon
Pawtucket Memorial Hospital, Pawtucket, Rhode Island
Medical University of South Carolina Hollings Cancer Center, Charleston, South Carolina
Santee Hematology Oncology, Sumter, South Carolina
Tenessee Cancer Specialists, Knoxville, Tennessee
Family Cancer Care, Memphis, Tennessee
Texas Oncology, Bedford, Texas
El Paso Cancer Treatment Center, El Paso, Texas
Texas Oncology-Allison Cancer Center, Midland, Texas
Southlake Oncology, Southlake, Texas
Utah Cancer Specialists, Salt Lake City, Utah
Charleston Area Medical Center, Health, Education, and Research Institute, Charleston, West Virginia
The Queen Elizabeth Hospital, North Adelaide, South Australia
Royal Melbourne Hospital, Parkville, Victoria
Affinity Research Limited, Nassau, CB
N.N. Aleksandrov National Cancer Center of Belarus, Lesnoy, Minsk Region
Institution Gomel Regional Clinical Oncology Dispensary, Gomel, Not set
Institution of Healthcare Grodno Regional Clinical Hospital, Grodno, Not set
Healthcare Institution Vitebsk Regional Clinical Oncology Dispensary, Vitebsk, Not set
Institut Jules Bordet, Brussels, Not set
District Dispensary for Oncology Diseases Internal Unit- Plovdiv EOOD, Plovdiv, Not set
District Dispensary for Oncology Diseases Internal Unit- Sofia EOOD, Sofia, Not set
Specialised Hospital of ActiveTreatment in Oncology, Clinic of Chemotherapy, Sofia, Not set
Hopital Charles, LeMoyne Le Centre Intégré de Cancérologie de la Montérégie, Greenfield Park, Quebec
Centre Hospitalier Régional de Trois-Rivières, Trois-Rivieres, Quebec
Sun Yat-Sen University Cancer Center, Guangzhou, Guangdong
Southern Medical University Nanfang Hospital, Guangzhou, Guangdong
Zhejiang Cancer Hospital, Hangzhou, Zhejiang
Cancer Hospital, Chinese Academy of Medical Sciences, Beijing, Not set
Peking Union Medical College Hospital of Chinese Academy of Medical Sciences, Beijing, Not set
The Hospital Affiliated Academy Military Medical Science, Chinese People's Liberation Army, Beijing, Not set
Chinese People's Liberation Army General Hospital, Beijing, Not set
Fudan University Shanghai Cancer Center, Shanghai, Not set
Tianjin Cancer Hospital, Tian Jin, Not set
Clinical Hospital Osijek, Department of Radiotherapy and Oncology, Osijek, Not set
University Hospital For Tumors, Zagreb, Not set
Rigshospitalet, Copenhagen, Onkologisk Klinik, Copenhagen, Not set
Hôpital Henri-Mondor, Creteil, Not set
Centre Leon Berard Departement de Cancerologie Medicale, Lyon, Not set
Centre Val d'Aurelle, Montpellier, Not set
Hopital Hotel Dieu, Service d'Oncologie Medicale, Bat B2, 5ieme, Paris, Not set
Hopital La Pitie-Salpetriere, Paris, Not set
Groupe Hospitalier Paris Saint Joseph, Oncologie medicale, Paris, Not set
Service d'Oncologie et de Radiotherapie, Polyclinique Francheville, Perigueux, Not set
Clinique Armoricaine de Radiologie, St. Brieuc, Not set
Centre de Radiothérapie, Clinique Sainte Anne, Service d'Oncologie Libérale, Strasbourg, Not set
CHU Strasbourg Departement Oncologie & Hematologie Hopital Civil, Strasbourg, Not set
CHU Bretonneau, Centre Henry Kaplan, Tours, Not set
Sozialstiftung Bamberg Klinik fuer Haematologie und internistische Onkologie, Bamberg, Not set
Pamela Youde Nethersole Eastern Hospital, Chai Wan, Not set
Queen Mary Hospital, Hong Kong, Not set
UNIMED Medical Institute, Comprehensive Centre for Breast Diseases, Wanchai, Not set
Semmelweis Egyetem Radiologiai és Onkoterapias Klinika, Budapest, Not set
Fovarosi Onkormanyzat Szent Imre Korhaz Klinikai Onkologiai Profil, Budapest, Not set
Orszagos Onkologiai Intezet "B" Belgyogyaszati osztaly, Budapest, Not set
Kaposi Mor Oktato Korhoz Onkologiai Centrum, Kaposvar, Not set
Bacs-Kiskun Megyei Onkormanyzat Korhaza Onkoradiologiai Kozpont, Kecskemet, Not set
Borsod-Abaúj-Zemplén Megyei Kórház és Egyetemi Oktató Kórház, Miskolc, Not set
Szegedi Tudomanyegyetem Onkoterapias Klinika, Szeged, Not set
Institute Rotary Cancer Hospital, AIIMS, New Delhi, Delhi
Jawaharlal Nehru Cancer Hospital, Bhopal, Madhya Pradesh
Tata Memorial Centre, Mumbai, Maharashtra
Central India Cancer Research Institute, Nagpur, Maharashtra
Curie Manavata Cancer Centre, Nashik, Maharashtra
Shatabdi Super Speciality Hospital, Nashilk, Maharashtra
Deenanath Mangeshkar Hospital and Research Centre, Pune, Maharashtra
Searoc Cancer Center, Jaipur, Rajasthan
Meenakshi Mission Hospital and Research Centre, Madurai, Tamil Nadu
B P Poddar and Medical Research Ltd., Kolkata, West Bengal
Kaplan Medical Center, Rehovot, Not set
Sourasky Medical Center, Tel Aviv, Not set
Assaf Harofeh Medical Center, Zerifin, Not set
Policlinico di Modena Oncologia ed Ematologia, Modena, Not set
Fondazione Salvatore Maugeri, Pavia, Not set
Policlinico Universitario Campus Bio-Medico, Roma, Not set
Ospedale San Pietro Fatebenefratelli, Roma, Not set
Ospedale San Giovanni Battista-Molinette, Torino, Not set
Hyogo Cancer Center, Hyogo, Akashi-shi
National Hospital Organization Beppu Medical Center, Oita, Beppu-shi
Tokyo Metropolitan Cancer and Infectious Disease Center, Komagome Hospital, Tokyo, Bunkyo-ku
Chiba Cancer Center, Chiba, Chiba-shi
National Hospital Organization Kyushu Cancer Center, Fukuoka, Fukuoka-shi
National Hospital Organization Mito Medical Center, Ibaraki, Higashiibaraki-gun
Hiroshima University Hospital, Hiroshima, Hiroshima-shi
Hakuaikai Medical Corporation Sagara Hospital, Kagoshima, Kagoshima-city
National Cancer Center Hospital East, Chiba, Kashiwa-shi
Saitama Cancer Center, Saitama, Kitaadachi-gun
Kumamoto Municipal Hospital, Kumamoto, Kumamoto-city
Kurume Daiichi Social Insurance Hospital, Fukuoka, Kurume-Shi
National Hospital Organization Shikoku Cancer Center, Ehime, Matsuyama-city
Iwate Medical University Hospital, Iwate, Morioka-shi
Aichi Cancer Center, Aichi, Nagoya-shi
National Hospital Organization Nagoya Medical Center, Aichi, Nagoya
Niigata Cancer Center Hospital, Niigata, Niigata-shi
Osaka Medical Center for Cancer and Cardiovascular Diseases, Osaka, Osaka-shi
National Hospital Organization Osaka National Hospital, Osaka, Osaka-shi
National Hospital Organization Hokkaido Cancer Center, Hokkaido, Sapporo-shi
Tohoku University Hospital, Miyagi, Sendai-city
Tenri Hospital, Nara, Tenri-shi
Kanagawa Cancer Center, Kanagawa, Yokohama-City
Hiroshima City Hospital, Hiroshima, Not set
National Hospital Organization Kure Medical Center and Chugoku Cancer Center, Hiroshima, Not set
Kobe City Medical Center General Hospital, Hyogo, Not set
Shinko Hospital, Hyogo, Not set
Kumamoto University Hospital, Kumamoto, Not set
Tazuke Kofukai Medical Research Institute Kitano Hospital, Osaka, Not set
Osaka University Hospital, Osaka, Not set
Jichi Medical University Hospital, Tochigi, Not set
Toranomon Hospital, Tokyo, Not set
National Hospital Organization Tokyo Medical Center, Tokyo, Not set
National Cancer Center, Center for Breast Cancer, Goyang-si, Gyeonggi-do
Samsung Medical Center, Seoul, Korea
Asan Medical Center, Seoul, Korea
Korea University Guro Hospital, Seoul, Korea
Yonsei University Health System Severance Hospital, Seoul, Seoul/Korea
Piejuras Hospital, Liepajas Oncological Clinic, Liepaja, Not set
Pauls Stradiņš Clinical University Hospital, Riga, Not set
Riga Eastern University Hospital, Riga, Not set
Hospital of Lithuanian University of Health sciences, Kaunas, Not set
Nacionalinis Vezio Institutas, Vilniaus Universiteto Onkologijos Institutas, Vilnius, Not set
University Malaya Medical Centre, Kuala Lumpur, Not set
Sir Anthony Oncology Center, Floriana, Not set
Samodzielny Publiczny Zaklad Opieki Zdrowotnej Szpital Wojewodzki Oddzial, Jelenia Gora, Dolnoslaskie
Magodent, Warszawa, Mazowieckie
Opolskie Centrum Onkologii, Opole, Opolskie
Zakład Opieki Zdrowotnej MSW z Warmińsko, Mazurskim Centrum Onkologii, Olsztyn, Warminsko-Mazurskie
Białostockie Centrum Onkologii, Bialystok, Not set
Hospital da Luz Servico de Oncologia Medica, Lisboa, Not set
Institutul Oncologic Prof. Dr. Ion Chiricuţă, Cluj-Napoca, Cluj
SC Oncolab S.R.L., Craiova, Dolj
Spitalul Universitar de Urgenta Bucuresti, Bucuresti, Not set
Institute of Oncology and Radiology of Serbia, Belgrade, Not set
Clinical centre Nis Clinic of Oncology, Nis, Not set
National University Hospital, National Cancer Institute, Singapore, Not set
National Cancer Centre Singapore, Singapore, Not set
GVI Oncology, Port Elizabeth, Eastern Cape
The Medical Oncology Centre of Rosebank, Johannesburg, Gauteng
University of Witwatersrand Oncology, Donald Gordon Medical Centre, Johannesburg, Gauteng
Sandton Oncology Centre, Johannesburg, Gauteng
Eastleigh Breast Care Centre, Pretoria, Gauteng
Westridge Medical Centre, Durban, KwaZulu Natal
GVI Oncology, Kraaifontein, Western Cape
Hospital Universitari Arnau de Vilanova, Lleida, Cataluna
Complejo Hospitalario Universitario Santiago de Compostela, Santiago de Compostela, Galicia
Hospital Son Llàtzer, Palma, Illes Balears
Hospital Universitario Fundación Alcorcón, Alcorcon, Madrid
Hospital Puerta De Hierro, Majadahonda, Madrid
Hospital Universitario Infanta Cristina, Parla, Madrid
Hospital Madrid Norte Sanchinarro Centro Integral Oncológico Clara Campal Ensayos Clínicos, Sanchinarro, Madrid
Hospital Costa del Sol, Marbella, Malaga
Hospital de Cruces, Baracaldo, Vizcaya
Centro Oncologico MD Anderson, Madrid, Not set
Hospital Universitario Ramón y Cajal, Madrid, Not set
Hospital Universitario 12 de Octubre, Madrid, Not set
Tumor Center Hirslanden Medical Center, Aarau, Not set
Spital STS AG Onkologiezentrum Thun - Berner Oberland, Thun, Not set
Kantonsspital Winterthur Medizinische Onkologie, Winterthur, Not set
Chang Gung Medical Foundation, Linkou Branch, Taoyuan, Not set
Ege Universitesi Tip Fakultesi Tulay Aktas Onkoloji Hastanesi, Bornova, Izmir
Komunalnyy Zaklad Cherkasskyy Oblasnyy Onkologichnyy Dyspanser, Cherkassy, Not set
Chernivtsi Regional Oncology Centre Outpatient Department Bukovynian State Medical University Department of Oncology and Radiology, Chernivtsi, Not set
City Multifield Clinical Hospital, Dnipropetrovsk, Not set
Donetsk Regional Antitumor Center Department of Pretumor Diseases and Tumor Treatment, Donetsk, Not set
S.P. Grigoreva Institute of Medical Radiology Department of Chemotherapy, Kharkiv, Not set
National Institute of Cancer Department of Conseravtive Methods of Treatment, Kyiv, Not set
Volyn Regional Oncological Center, Lutsk, Not set
State Oncological Regional Treatment and Diagnostic Center, Lviv, Not set
Mariupil Oncological Center, Mariupil, Not set
Sumy Regional Clinical Oncology Centre, Sumy, Not set
Guy's and St Thomas NHS Foundation Trust Management Offices 4th Floor Bermondsey Wing Guy's Hospital, London, Not set
Nottingham University Hospital, Nottingham, Not set
Conditions: Breast Cancer
Study of Efficacy and Safety of Buparlisib (BKM120) Plus Paclitaxel Versus Placebo Plus Paclitaxel in Recurrent or Metastatic Head and Neck Cancer Previously Pre-treated With a Platinum Therapy
Terminated
Phase II Study of efficacy and safety of buparlisib (BKM120) plus paclitaxel versus placebo plus paclitaxel in recurrent or metastatic Head and Neck cancer previously pre-treated with a platinum therapy.The primary endpoint was PFS and the key secondary endpoint was Overall Survival.
Phase II Study of efficacy and safety of buparlisib (BKM120) plus paclitaxel versus placebo plus paclitaxel in recurrent or metastatic Head and Neck cancer previously pre-treated with a platinum therapy.The primary endpoint was PFS and the key secondary endpoint was Overall Survival. Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
06/26/2018
Locations: Highlands Oncology Group, Fayetteville, Arkansas +57 locations
Highlands Oncology Group, Fayetteville, Arkansas
Dana Farber Cancer Institute IRB, Boston, Massachusetts
Washington U School of Medicine Center for Clinical Studies SC - BKM120H2201, Saint Louis, Missouri
The Mount Sinai Hospital Dept of Oncology, New York, New York
University of N.C. at Chapel Hill Lineberger Comp. Cancer Ctr., Chapel Hill, North Carolina
University Hospitals Case Medical Center Univ. Hospitals of Cleveland, Cleveland, Ohio
UPMC Cancer Centers BKM120H2201, Pittsburgh, Pennsylvania
Novartis Investigative Site, St Leonards, New South Wales
Novartis Investigative Site, Hamilton, Ontario
Novartis Investigative Site, Montreal, Quebec
Novartis Investigative Site, Saint Herblain cedex, Not set
Novartis Investigative Site, Berlin, Not set
Novartis Investigative Site, Essen, Not set
Novartis Investigative Site, Hannover, Not set
Novartis Investigative Site, Budapest, Not set
Novartis Investigative Site, Budapest, Not set
Novartis Investigative Site, Budapest, Not set
Novartis Investigative Site, Nyiregyhaza, Not set
Novartis Investigative Site, Nashik, Maharashtra
Novartis Investigative Site, Dehli, New Delhi
Novartis Investigative Site, Jaipur, Rajasthan
Novartis Investigative Site, Kolkata, West Bengal
Novartis Investigative Site, Kerala, Not set
Novartis Investigative Site, Mumbai, Not set
Novartis Investigative Site, Dublin 4, Not set
Novartis Investigative Site, Firenze, FI
Novartis Investigative Site, Milano, MI
Novartis Investigative Site, Milano, MI
Novartis Investigative Site, Milano, MI
Novartis Investigative Site, Palermo, PA
Novartis Investigative Site, Roma, RM
Novartis Investigative Site, Salerno, SA
Novartis Investigative Site, Torino, TO
Novartis Investigative Site, Venezia, VE
Novartis Investigative Site, Kashiwa, Chiba
Novartis Investigative Site, Koto-ku, Tokyo
Novartis Investigative Site, Minato-ku, Tokyo
Novartis Investigative Site, Seoul, Korea
Novartis Investigative Site, Seoul, Seocho-gu
Novartis Investigative Site, Warszawa, Not set
Novartis Investigative Site, Leningrad Region, Russia
Novartis Investigative Site, Nizhniy Novgorod, Not set
Novartis Investigative Site, St. Petersburg, Not set
Novartis Investigative Site, Barcelona, Catalunya
Novartis Investigative Site, Hospitalet de LLobregat, Catalunya
Novartis Investigative Site, Madrid, Not set
Novartis Investigative Site, Basel, Not set
Novartis Investigative Site, Genève, Not set
Novartis Investigative Site, Tainan, Taiwan ROC
Novartis Investigative Site, Kaohsiung City, Not set
Novartis Investigative Site, Taichung City, Not set
Novartis Investigative Site, Songkla, Hat Yai
Novartis Investigative Site, Bangkok, Not set
Novartis Investigative Site, Bangkok, Not set
Novartis Investigative Site, Glasgow, Scotland
Novartis Investigative Site, London, Not set
Novartis Investigative Site, London, Not set
Novartis Investigative Site, Manchester, Not set
Conditions: Head and Neck Squamous Cell Carcinoma
A Study of Tasisulam-sodium Versus Paclitaxel as Treatment for Metastatic Melanoma
Terminated
The primary purpose of this study was to see how tasisulam-sodium affected metastatic melanoma when compared against paclitaxel as measured by overall survival.
The primary purpose of this study was to see how tasisulam-sodium affected metastatic melanoma when compared against paclitaxel as measured by overall survival. Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
06/18/2018
Locations: For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Birmingham, Alabama +121 locations
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Birmingham, Alabama
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Scottsdale, Arizona
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Tucson, Arizona
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Little Rock, Arkansas
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Fresno, California
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Los Angeles, California
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., San Francisco, California
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Fort Myers, Florida
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Jacksonville, Florida
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Lakeland, Florida
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Orlando, Florida
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., West Palm Beach, Florida
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Augusta, Georgia
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Chicago, Illinois
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Park Ridge, Illinois
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Goshen, Indiana
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Indianapolis, Indiana
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Iowa City, Iowa
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Westwood, Kansas
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Wichita, Kansas
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Louisville, Kentucky
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Baton Rouge, Louisiana
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Minneapolis, Minnesota
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Rochester, Minnesota
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Columbia, Missouri
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Saint Louis, Missouri
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Omaha, Nebraska
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Las Vegas, Nevada
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Morristown, New Jersey
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Durham, North Carolina
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Winston-Salem, North Carolina
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Fargo, North Dakota
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Cincinnati, Ohio
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Cleveland, Ohio
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Columbus, Ohio
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Toledo, Ohio
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Bethlehem, Pennsylvania
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Pittsburgh, Pennsylvania
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Charleston, South Carolina
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Columbia, South Carolina
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Rapid City, South Dakota
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Memphis, Tennessee
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Nashville, Tennessee
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Dallas, Texas
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., La Porte, Texas
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., The Woodlands, Texas
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Salt Lake City, Utah
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Richmond, Virginia
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Seattle, Washington
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Madison, Wisconsin
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Coffs Harbour, New South Wales
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Wollongong, New South Wales
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Townsville, Queensland
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Woolloongabba, Queensland
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Nedlands, Western Australia
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Graz, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Innsbruck, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Vienna, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Antwerp, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Brussels, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Leuven, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Edmonton, Alberta
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Hamilton, Ontario
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Toronto, Ontario
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Montreal, Quebec
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Tampere, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Turku, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Bordeaux, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Dijon, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Grenoble, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Marseille, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Nantes, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Paris, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Toulouse, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Villejuif, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Berlin, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Buxtehude, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Essen, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Hannover, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Heilbronn, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Kiel, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Koeln, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Mainz, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Muenchen, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Muenster, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Quedlinburg, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Tuebingen, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Jerusalem, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Tel Hashomer, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Tel-Aviv, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Genova, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Milano, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Napoli, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Padova, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Siena, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Goyang-Si, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Seoul, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Leiden, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Maastricht, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Rotterdam, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Oslo, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Trondheim, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Bialystok, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Gdansk, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Otwock, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Poznan, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Barcelona, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Madrid, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Pamplona, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Valencia, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Malmo, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Stockholm, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Changhua, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Niao Sung Hsiang, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Taipei, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Tao-Yuan, Not set
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Cambridge, Cambridgeshire
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., London, Greater London
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Southampton, Hants
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Hampstead, London
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Northwood, Middlesex
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Manchester, Not set
Conditions: Melanoma
F16IL2 Plus Paclitaxel in Metastatic Merkel Cell Carcinoma
Terminated
There is no standard treatment for Merkel cell carcinoma(MCC), as no randomized trials have been conducted to establish standard of care. Despite a sizable number of objective responses induced by combination cyototoxic chemotherapy, a prolongation of patients overall survival has never been demonstrated.
This open-label, randomized, double-arm, multi-centre, phase II study of F16IL2 in combination with paclitaxel versus paclitaxel monotherapy, proposes to test the therapeutic efficacy of F16IL... Read More
There is no standard treatment for Merkel cell carcinoma(MCC), as no randomized trials have been conducted to establish standard of care. Despite a sizable number of objective responses induced by combination cyototoxic chemotherapy, a prolongation of patients overall survival has never been demonstrated.
This open-label, randomized, double-arm, multi-centre, phase II study of F16IL2 in combination with paclitaxel versus paclitaxel monotherapy, proposes to test the therapeutic efficacy of F16IL2 plus paclitaxel in patients with metastatic Merkel cell carcinoma, who are not amenable to surgery.
A total of 90 patients with Merkel cell carcinoma will be enrolled and treated during the study; 45 patients will receive the combination treatment of F16IL2 and paclitaxel (Arm A), and 45 patients will receive paclitaxel monotherapy (Arm B). Read Less
Gender:
ALL
Ages:
Between 18 years and 75 years
Trial Updated:
05/15/2018
Locations: Medical University Hospital, Graz, Not set +7 locations
Medical University Hospital, Graz, Not set
Herlev- University Hospital, Herlev, Not set
Saint-Louis- Hospital, Paris, Not set
Charité- Medical University Hospital, Berlin, Not set
Universitätsklinik Essen, Essen, Not set
Eberhard-Karls- University Hospital, Tübingen, Not set
ICMiD- University Hospital, Barcelona, Not set
Nottingham Trent- University Hospital, Nottingham, Not set
Conditions: Merkel Cell Carcinoma
Study of Pazopanib and Paclitaxel in Advanced Non-small Cell Lung Cancer
Completed
The Phase I part of the study will identify the doses of pazopanib and paclitaxel that can be administered safely in combination. The Phase II part of the study will not be progressed as documented in Protocol Amendment 01.
The Phase I part of the study will identify the doses of pazopanib and paclitaxel that can be administered safely in combination. The Phase II part of the study will not be progressed as documented in Protocol Amendment 01. Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
11/08/2017
Locations: GSK Investigational Site, Chicago, Illinois +3 locations
GSK Investigational Site, Chicago, Illinois
GSK Investigational Site, Columbus, Ohio
GSK Investigational Site, Sutton, Surrey
GSK Investigational Site, Newcastle upon Tyne, Not set
Conditions: Lung Cancer, Non-Small Cell
LUME-Ovar 1: Nintedanib (BIBF 1120) or Placebo in Combination With Paclitaxel and Carboplatin in First Line Treatment of Ovarian Cancer
Completed
The trial will be performed to evaluate if BIBF 1120 in combination with paclitaxel and carboplatin is more effective than placebo in combination with paclitaxel and carboplatin in first-line treatment of patients with advanced ovarian cancer. Safety information about BIBF1120/paclitaxel/carboplatin will be obtained.
The trial will be performed to evaluate if BIBF 1120 in combination with paclitaxel and carboplatin is more effective than placebo in combination with paclitaxel and carboplatin in first-line treatment of patients with advanced ovarian cancer. Safety information about BIBF1120/paclitaxel/carboplatin will be obtained. Read Less
Gender:
FEMALE
Ages:
18 years and above
Trial Updated:
11/03/2017
Locations: 1199.15.10113 Boehringer Ingelheim Investigational Site, Tucson, Arizona +280 locations
1199.15.10113 Boehringer Ingelheim Investigational Site, Tucson, Arizona
1199.15.10030 Boehringer Ingelheim Investigational Site, Long Beach, California
1199.15.10001 Boehringer Ingelheim Investigational Site, Santa Rosa, California
1199.15.10005 Boehringer Ingelheim Investigational Site, Englewood, Colorado
1199.15.10028 Boehringer Ingelheim Investigational Site, New Haven, Connecticut
1199.15.10014 Boehringer Ingelheim Investigational Site, Orlando, Florida
1199.15.10010 Boehringer Ingelheim Investigational Site, Augusta, Georgia
1199.15.10004 Boehringer Ingelheim Investigational Site, Savannah, Georgia
1199.15.10011 Boehringer Ingelheim Investigational Site, Louisville, Kentucky
1199.15.10003 Boehringer Ingelheim Investigational Site, Marrero, Louisiana
1199.15.10017 Boehringer Ingelheim Investigational Site, Detroit, Michigan
1199.15.10103 Boehringer Ingelheim Investigational Site, Minneapolis, Minnesota
1199.15.10002 Boehringer Ingelheim Investigational Site, New York, New York
1199.15.10012 Boehringer Ingelheim Investigational Site, Charlotte, North Carolina
1199.15.10020 Boehringer Ingelheim Investigational Site, Winston-Salem, North Carolina
1199.15.10019 Boehringer Ingelheim Investigational Site, Bismarck, North Dakota
1199.15.10024 Boehringer Ingelheim Investigational Site, Canton, Ohio
1199.15.10025 Boehringer Ingelheim Investigational Site, Cleveland, Ohio
1199.15.10029 Boehringer Ingelheim Investigational Site, Cleveland, Ohio
1199.15.10021 Boehringer Ingelheim Investigational Site, Portland, Oregon
1199.15.10013 Boehringer Ingelheim Investigational Site, Abington, Pennsylvania
1199.15.10016 Boehringer Ingelheim Investigational Site, Allentown, Pennsylvania
1199.15.10008 Boehringer Ingelheim Investigational Site, Providence, Rhode Island
1199.15.10102 Boehringer Ingelheim Investigational Site, Greenville, South Carolina
1199.15.10006 Boehringer Ingelheim Investigational Site, Chattanooga, Tennessee
1199.15.10104 Boehringer Ingelheim Investigational Site, Austin, Texas
1199.15.10100 Boehringer Ingelheim Investigational Site, Bedford, Texas
1199.15.10107 Boehringer Ingelheim Investigational Site, Dallas, Texas
1199.15.10108 Boehringer Ingelheim Investigational Site, Dallas, Texas
1199.15.10110 Boehringer Ingelheim Investigational Site, Fort Worth, Texas
1199.15.10007 Boehringer Ingelheim Investigational Site, Houston, Texas
1199.15.10105 Boehringer Ingelheim Investigational Site, Spokane, Washington
1199.15.10112 Boehringer Ingelheim Investigational Site, Vancouver, Washington
1199.15.61006 Boehringer Ingelheim Investigational Site, Camperdown, New South Wales
1199.15.61001 Boehringer Ingelheim Investigational Site, Waratah, New South Wales
1199.15.61004 Boehringer Ingelheim Investigational Site, Herston, Queensland
1199.15.61003 Boehringer Ingelheim Investigational Site, Southe Brisbane, Queensland
1199.15.61005 Boehringer Ingelheim Investigational Site, North Terrace, South Australia
1199.15.61007 Boehringer Ingelheim Investigational Site, Parkville, Victoria
1199.15.61002 Boehringer Ingelheim Investigational Site, Nedlands, Western Australia
1199.15.43003 Boehringer Ingelheim Investigational Site, Graz, Not set
1199.15.43001 Boehringer Ingelheim Investigational Site, Innsbruck, Not set
1199.15.43011 Boehringer Ingelheim Investigational Site, Krems, Not set
1199.15.43007 Boehringer Ingelheim Investigational Site, Kufstein, Not set
1199.15.43005 Boehringer Ingelheim Investigational Site, Linz, Not set
1199.15.43010 Boehringer Ingelheim Investigational Site, Salzburg, Not set
1199.15.43013 Boehringer Ingelheim Investigational Site, Wels, Not set
1199.15.43002 Boehringer Ingelheim Investigational Site, Wien, Not set
1199.15.43012 Boehringer Ingelheim Investigational Site, Wien, Not set
1199.15.32010 Boehringer Ingelheim Investigational Site, Edegem, Not set
1199.15.32012 Boehringer Ingelheim Investigational Site, Hasselt, Not set
1199.15.32003 Boehringer Ingelheim Investigational Site, La Louvière, Not set
1199.15.32001 Boehringer Ingelheim Investigational Site, Leuven, Not set
1199.15.32007 Boehringer Ingelheim Investigational Site, Liège, Not set
1199.15.32008 Boehringer Ingelheim Investigational Site, Sint-Niklaas, Not set
1199.15.11005 Boehringer Ingelheim Investigational Site, Vancouver, British Columbia
1199.15.11004 Boehringer Ingelheim Investigational Site, Hamilton, Ontario
1199.15.11008 Boehringer Ingelheim Investigational Site, London, Ontario
1199.15.11009 Boehringer Ingelheim Investigational Site, Toronto, Ontario
1199.15.11003 Boehringer Ingelheim Investigational Site, Montreal, Quebec
1199.15.11006 Boehringer Ingelheim Investigational Site, Montreal, Quebec
1199.15.11001 Boehringer Ingelheim Investigational Site, Sherbrooke, Quebec
1199.15.42002 Boehringer Ingelheim Investigational Site, Brno, Not set
1199.15.42003 Boehringer Ingelheim Investigational Site, Olomouc, Not set
1199.15.42001 Boehringer Ingelheim Investigational Site, Prague, Not set
1199.15.45004 Boehringer Ingelheim Investigational Site, Aalborg, Not set
1199.15.45002 Boehringer Ingelheim Investigational Site, Herlev, Not set
1199.15.45005 Boehringer Ingelheim Investigational Site, Herning, Not set
1199.15.45001 Boehringer Ingelheim Investigational Site, Købenahvn Ø, Not set
1199.15.45003 Boehringer Ingelheim Investigational Site, Odense C, Not set
1199.15.35801 Boehringer Ingelheim Investigational Site, Helsinki, Not set
1199.15.35804 Boehringer Ingelheim Investigational Site, Jyväskylä, Not set
1199.15.35805 Boehringer Ingelheim Investigational Site, Kuopio, Not set
1199.15.35803 Boehringer Ingelheim Investigational Site, Oulu, Not set
1199.15.35802 Boehringer Ingelheim Investigational Site, Tampere, Not set
1199.15.33047 Boehringer Ingelheim Investigational Site, Aix-en-Provence, Not set
1199.15.33035 Boehringer Ingelheim Investigational Site, Avignon cedex 02, Not set
1199.15.33055 Boehringer Ingelheim Investigational Site, Besançon, Not set
1199.15.33003 Boehringer Ingelheim Investigational Site, Bordeaux cedex, Not set
1199.15.33004 Boehringer Ingelheim Investigational Site, Bordeaux, Not set
1199.15.33006 Boehringer Ingelheim Investigational Site, Caen cedex 5, Not set
1199.15.33025 Boehringer Ingelheim Investigational Site, Clermont-Ferrand cedex, Not set
1199.15.33048 Boehringer Ingelheim Investigational Site, Dechy, Not set
1199.15.33042 Boehringer Ingelheim Investigational Site, Fréjus, Not set
1199.15.33037 Boehringer Ingelheim Investigational Site, La Roche-Sur-Yon cedex 09, Not set
1199.15.33008 Boehringer Ingelheim Investigational Site, Le Mans, Not set
1199.15.33009 Boehringer Ingelheim Investigational Site, Lille cedex, Not set
1199.15.33020 Boehringer Ingelheim Investigational Site, Lyon, Not set
1199.15.33011 Boehringer Ingelheim Investigational Site, Marseille cedex 09, Not set
1199.15.33021 Boehringer Ingelheim Investigational Site, Monaco Cedex, Not set
1199.15.33012 Boehringer Ingelheim Investigational Site, Mont-de-Marsan cedex, Not set
1199.15.33052 Boehringer Ingelheim Investigational Site, Montpellier cedex 5, Not set
1199.15.33053 Boehringer Ingelheim Investigational Site, Mougins, Not set
1199.15.33038 Boehringer Ingelheim Investigational Site, Nancy, Not set
1199.15.33013 Boehringer Ingelheim Investigational Site, Nantes cedex 02, Not set
1199.15.33015 Boehringer Ingelheim Investigational Site, Orléans cedex 02, Not set
1199.15.33027 Boehringer Ingelheim Investigational Site, Paris cedex 20, Not set
1199.15.33001 Boehringer Ingelheim Investigational Site, Paris, Not set
1199.15.33051 Boehringer Ingelheim Investigational Site, PERIGUEUX Cedex, Not set
1199.15.33030 Boehringer Ingelheim Investigational Site, Plerin SUR MER, Not set
1199.15.33045 Boehringer Ingelheim Investigational Site, Saint Cloud, Not set
1199.15.33033 Boehringer Ingelheim Investigational Site, Saint-Herblain cedex, Not set
1199.15.33018 Boehringer Ingelheim Investigational Site, Strasbourg cedex, Not set
1199.15.33039 Boehringer Ingelheim Investigational Site, Thonon-Les-Bains, Not set
1199.15.33031 Boehringer Ingelheim Investigational Site, Vandoeuvre les Nancy cedex, Not set
1199.15.33050 Boehringer Ingelheim Investigational Site, Villejuif Cedex, Not set
1199.15.49040 Boehringer Ingelheim Investigational Site, Aachen, Not set
1199.15.49070 Boehringer Ingelheim Investigational Site, Aalen, Not set
1199.15.49086 Boehringer Ingelheim Investigational Site, Aschaffenburg, Not set
1199.15.49002 Boehringer Ingelheim Investigational Site, Berlin, Not set
1199.15.49039 Boehringer Ingelheim Investigational Site, Berlin, Not set
1199.15.49041 Boehringer Ingelheim Investigational Site, Berlin, Not set
1199.15.49004 Boehringer Ingelheim Investigational Site, Bonn, Not set
1199.15.49042 Boehringer Ingelheim Investigational Site, Bonn, Not set
1199.15.49071 Boehringer Ingelheim Investigational Site, Bottrop, Not set
1199.15.49081 Boehringer Ingelheim Investigational Site, Böblingen, Not set
1199.15.49043 Boehringer Ingelheim Investigational Site, Chemnitz, Not set
1199.15.49005 Boehringer Ingelheim Investigational Site, Dessau, Not set
1199.15.49006 Boehringer Ingelheim Investigational Site, Detmold, Not set
1199.15.49007 Boehringer Ingelheim Investigational Site, Dresden, Not set
1199.15.49067 Boehringer Ingelheim Investigational Site, Dresden, Not set
1199.15.49008 Boehringer Ingelheim Investigational Site, Düsseldorf, Not set
1199.15.49009 Boehringer Ingelheim Investigational Site, Ebersberg, Not set
1199.15.49010 Boehringer Ingelheim Investigational Site, Essen, Not set
1199.15.49066 Boehringer Ingelheim Investigational Site, Essen, Not set
1199.15.49089 Boehringer Ingelheim Investigational Site, Essen, Not set
1199.15.49045 Boehringer Ingelheim Investigational Site, Frankfurt, Not set
1199.15.49011 Boehringer Ingelheim Investigational Site, Freiburg, Not set
1199.15.49068 Boehringer Ingelheim Investigational Site, Freiburg, Not set
1199.15.49083 Boehringer Ingelheim Investigational Site, Freudenstadt, Not set
1199.15.49046 Boehringer Ingelheim Investigational Site, Fulda, Not set
1199.15.49012 Boehringer Ingelheim Investigational Site, Fürstenfeldbruck, Not set
1199.15.49064 Boehringer Ingelheim Investigational Site, Greifswald, Not set
1199.15.49076 Boehringer Ingelheim Investigational Site, Gütersloh, Not set
1199.15.49014 Boehringer Ingelheim Investigational Site, Halle/S., Not set
1199.15.49015 Boehringer Ingelheim Investigational Site, Hamburg, Not set
1199.15.49084 Boehringer Ingelheim Investigational Site, Hamburg, Not set
1199.15.49073 Boehringer Ingelheim Investigational Site, Hanau, Not set
1199.15.49095 Boehringer Ingelheim Investigational Site, Heidelberg, Not set
1199.15.49080 Boehringer Ingelheim Investigational Site, Henstedt-Ulzburg, Not set
1199.15.49047 Boehringer Ingelheim Investigational Site, Hildesheim, Not set
1199.15.49016 Boehringer Ingelheim Investigational Site, Karlsruhe, Not set
1199.15.49017 Boehringer Ingelheim Investigational Site, Kiel, Not set
1199.15.49062 Boehringer Ingelheim Investigational Site, Krefeld, Not set
1199.15.49018 Boehringer Ingelheim Investigational Site, Landshut, Not set
1199.15.49087 Boehringer Ingelheim Investigational Site, Ludwigsburg, Not set
1199.15.49019 Boehringer Ingelheim Investigational Site, Lübeck, Not set
1199.15.49020 Boehringer Ingelheim Investigational Site, Magdeburg, Not set
1199.15.49021 Boehringer Ingelheim Investigational Site, Mainz, Not set
1199.15.49022 Boehringer Ingelheim Investigational Site, Mainz, Not set
1199.15.49023 Boehringer Ingelheim Investigational Site, Mannheim, Not set
1199.15.49024 Boehringer Ingelheim Investigational Site, Marburg, Not set
1199.15.49025 Boehringer Ingelheim Investigational Site, München, Not set
1199.15.49026 Boehringer Ingelheim Investigational Site, München, Not set
1199.15.49027 Boehringer Ingelheim Investigational Site, München, Not set
1199.15.49048 Boehringer Ingelheim Investigational Site, München, Not set
1199.15.49065 Boehringer Ingelheim Investigational Site, Neumarkt i.d.Opf., Not set
1199.15.49029 Boehringer Ingelheim Investigational Site, Offenbach, Not set
1199.15.49082 Boehringer Ingelheim Investigational Site, Paderborn, Not set
1199.15.49030 Boehringer Ingelheim Investigational Site, Radebeul, Not set
1199.15.49061 Boehringer Ingelheim Investigational Site, Ravensburg, Not set
1199.15.49050 Boehringer Ingelheim Investigational Site, Regensburg, Not set
1199.15.49051 Boehringer Ingelheim Investigational Site, Rosenheim, Not set
1199.15.49052 Boehringer Ingelheim Investigational Site, Rostock, Not set
1199.15.49054 Boehringer Ingelheim Investigational Site, Saalfeld, Not set
1199.15.49031 Boehringer Ingelheim Investigational Site, Salzgitter, Not set
1199.15.49055 Boehringer Ingelheim Investigational Site, Solingen, Not set
1199.15.49092 Boehringer Ingelheim Investigational Site, Stadthagen, Not set
1199.15.49063 Boehringer Ingelheim Investigational Site, Stendal, Not set
1199.15.49093 Boehringer Ingelheim Investigational Site, Stralsund, Not set
1199.15.49033 Boehringer Ingelheim Investigational Site, Stuttgart, Not set
1199.15.49056 Boehringer Ingelheim Investigational Site, Stuttgart, Not set
1199.15.49090 Boehringer Ingelheim Investigational Site, Stuttgart, Not set
1199.15.49079 Boehringer Ingelheim Investigational Site, Suhl, Not set
1199.15.49034 Boehringer Ingelheim Investigational Site, Traunstein, Not set
1199.15.49057 Boehringer Ingelheim Investigational Site, Trier, Not set
1199.15.49035 Boehringer Ingelheim Investigational Site, Tübingen, Not set
1199.15.49058 Boehringer Ingelheim Investigational Site, Ulm, Not set
1199.15.49085 Boehringer Ingelheim Investigational Site, Viersen, Not set
1199.15.49001 Boehringer Ingelheim Investigational Site, Wiesbaden, Not set
1199.15.49036 Boehringer Ingelheim Investigational Site, Wiesbaden, Not set
1199.15.49059 Boehringer Ingelheim Investigational Site, Witten, Not set
1199.15.49037 Boehringer Ingelheim Investigational Site, Wolfsburg, Not set
1199.15.49060 Boehringer Ingelheim Investigational Site, Worms, Not set
1199.15.30001 Boehringer Ingelheim Investigational Site, Athens, Not set
1199.15.30003 Boehringer Ingelheim Investigational Site, Heraklio, Not set
1199.15.30002 Boehringer Ingelheim Investigational Site, Nea Kifisia, Not set
1199.15.30005 Boehringer Ingelheim Investigational Site, Patras, Not set
1199.15.30004 Boehringer Ingelheim Investigational Site, Thessaloniki, Not set
1199.15.39027 Boehringer Ingelheim Investigational Site, Asti, Not set
1199.15.39002 Boehringer Ingelheim Investigational Site, Avellino, Not set
1199.15.39003 Boehringer Ingelheim Investigational Site, Aviano (pn), Not set
1199.15.39004 Boehringer Ingelheim Investigational Site, Bari, Not set
1199.15.39005 Boehringer Ingelheim Investigational Site, Benevento, Not set
1199.15.39029 Boehringer Ingelheim Investigational Site, Brescia, Not set
1199.15.39040 Boehringer Ingelheim Investigational Site, Catania, Not set
1199.15.39007 Boehringer Ingelheim Investigational Site, Catanzaro, Not set
1199.15.39008 Boehringer Ingelheim Investigational Site, Faenza (RA), Not set
1199.15.39039 Boehringer Ingelheim Investigational Site, Ferrara, Not set
1199.15.39017 Boehringer Ingelheim Investigational Site, Genova, Not set
1199.15.39037 Boehringer Ingelheim Investigational Site, Lecce, Not set
1199.15.39009 Boehringer Ingelheim Investigational Site, Mantova, Not set
1199.15.39033 Boehringer Ingelheim Investigational Site, Meldola (fc), Not set
1199.15.39021 Boehringer Ingelheim Investigational Site, Milano, Not set
1199.15.39028 Boehringer Ingelheim Investigational Site, Milano, Not set
1199.15.39036 Boehringer Ingelheim Investigational Site, Milano, Not set
1199.15.39010 Boehringer Ingelheim Investigational Site, Modena, Not set
1199.15.39026 Boehringer Ingelheim Investigational Site, Monza, Not set
1199.15.39001 Boehringer Ingelheim Investigational Site, Napoli, Not set
1199.15.39022 Boehringer Ingelheim Investigational Site, Padova, Not set
1199.15.39011 Boehringer Ingelheim Investigational Site, Palermo, Not set
1199.15.39031 Boehringer Ingelheim Investigational Site, Palermo, Not set
1199.15.39023 Boehringer Ingelheim Investigational Site, Pisa, Not set
1199.15.39012 Boehringer Ingelheim Investigational Site, Pordenone, Not set
1199.15.39024 Boehringer Ingelheim Investigational Site, Reggio Emilia, Not set
1199.15.39013 Boehringer Ingelheim Investigational Site, Roma, Not set
1199.15.39014 Boehringer Ingelheim Investigational Site, Roma, Not set
1199.15.39034 Boehringer Ingelheim Investigational Site, Rozzano (MI), Not set
1199.15.39030 Boehringer Ingelheim Investigational Site, San Fermo Della Battaglia, Not set
1199.15.39018 Boehringer Ingelheim Investigational Site, Sondrio, Not set
1199.15.39006 Boehringer Ingelheim Investigational Site, Tappino (CB), Not set
1199.15.39019 Boehringer Ingelheim Investigational Site, Torino, Not set
1199.15.39020 Boehringer Ingelheim Investigational Site, Torino, Not set
1199.15.39032 Boehringer Ingelheim Investigational Site, Varese, Not set
1199.15.31009 Boehringer Ingelheim Investigational Site, 's-HERTOGENBOSCH, Not set
1199.15.31005 Boehringer Ingelheim Investigational Site, Amersfoort, Not set
1199.15.31004 Boehringer Ingelheim Investigational Site, Niewegein, Not set
1199.15.31003 Boehringer Ingelheim Investigational Site, Nijmegen, Not set
1199.15.31006 Boehringer Ingelheim Investigational Site, Rotterdam, Not set
1199.15.31002 Boehringer Ingelheim Investigational Site, Utrecht, Not set
1199.15.47003 Boehringer Ingelheim Investigational Site, Bergen, Not set
1199.15.47001 Boehringer Ingelheim Investigational Site, Oslo, Not set
1199.15.47002 Boehringer Ingelheim Investigational Site, Stavanger, Not set
1199.15.47004 Boehringer Ingelheim Investigational Site, Trondheim, Not set
1199.15.48003 Boehringer Ingelheim Investigational Site, Gdansk, Not set
1199.15.48006 Boehringer Ingelheim Investigational Site, Lublin, Not set
1199.15.48001 Boehringer Ingelheim Investigational Site, Warszawa, Not set
1199.15.35102 Boehringer Ingelheim Investigational Site, Coimbra, Not set
1199.15.35104 Boehringer Ingelheim Investigational Site, Coimbra, Not set
1199.15.35101 Instituto Portugues de Oncologia Lisboa Francisco Gentil, Lisboa, Not set
1199.15.35106 Boehringer Ingelheim Investigational Site, Lisboa, Not set
1199.15.35108 Boehringer Ingelheim Investigational Site, Lisboa, Not set
1199.15.35105 Boehringer Ingelheim Investigational Site, Porto, Not set
1199.15.35109 Boehringer Ingelheim Investigational Site, Vila Real, Not set
1199.15.70006 Boehringer Ingelheim Investigational Site, Barnaul, Not set
1199.15.70005 Boehringer Ingelheim Investigational Site, Ekaterinburg, Not set
1199.15.70007 Boehringer Ingelheim Investigational Site, Kazan, Not set
1199.15.70001 Boehringer Ingelheim Investigational Site, Moscow, Not set
1199.15.70002 Boehringer Ingelheim Investigational Site, St. Petersburg, Not set
1199.15.42101 Boehringer Ingelheim Investigational Site, Bratislava, Not set
1199.15.42105 Boehringer Ingelheim Investigational Site, Bratislava, Not set
1199.15.42106 Boehringer Ingelheim Investigational Site, Kosice, Not set
1199.15.42103 Boehringer Ingelheim Investigational Site, Nitra, Not set
1199.15.42104 Boehringer Ingelheim Investigational Site, Poprad, Not set
1199.15.42102 Boehringer Ingelheim Investigational Site, Zilina, Not set
1199.15.34001 Boehringer Ingelheim Investigational Site, Badalona, Not set
1199.15.34003 Boehringer Ingelheim Investigational Site, Barcelona, Not set
1199.15.34006 Boehringer Ingelheim Investigational Site, Girona, Not set
1199.15.34004 Boehringer Ingelheim Investigational Site, Lleida, Not set
1199.15.34002 Boehringer Ingelheim Investigational Site, Madrid, Not set
1199.15.34010 Boehringer Ingelheim Investigational Site, Madrid, Not set
1199.15.34005 Boehringer Ingelheim Investigational Site, Palma de Mallorca, Not set
1199.15.34009 Boehringer Ingelheim Investigational Site, Valencia, Not set
1199.15.46005 Boehringer Ingelheim Investigational Site, Linköping, Not set
1199.15.46001 Boehringer Ingelheim Investigational Site, Lund, Not set
1199.15.46002 Boehringer Ingelheim Investigational Site, Stockholm, Not set
1199.15.46004 Boehringer Ingelheim Investigational Site, Umeå, Not set
1199.15.46003 Boehringer Ingelheim Investigational Site, Uppsala, Not set
1199.15.38006 Boehringer Ingelheim Investigational Site, Cherkasy, Not set
1199.15.38005 Boehringer Ingelheim Investigational Site, Dnepropetrovsk, Not set
1199.15.38004 Boehringer Ingelheim Investigational Site, Donetsk, Not set
1199.15.38002 Boehringer Ingelheim Investigational Site, Kharkiv, Not set
1199.15.38003 Boehringer Ingelheim Investigational Site, Lviv, Not set
1199.15.44006 Boehringer Ingelheim Investigational Site, Derby, Not set
1199.15.44007 Boehringer Ingelheim Investigational Site, Dundee, Not set
1199.15.44003 Boehringer Ingelheim Investigational Site, Glasgow, Not set
1199.15.44001 Boehringer Ingelheim Investigational Site, Guildford, Not set
1199.15.44005 Boehringer Ingelheim Investigational Site, London, Not set
1199.15.44004 Boehringer Ingelheim Investigational Site, Nottingham, Not set
1199.15.44002 Boehringer Ingelheim Investigational Site, Poole, Not set
1199.15.44008 Boehringer Ingelheim Investigational Site, Truro, Not set
Conditions: Ovarian Neoplasms, Peritoneal Neoplasms
A Study of First Line Treatment With Avastin (Bevacizumab) in Combination With Carboplatin and Weekly Paclitaxel in Patients With Ovarian Cancer
Completed
This single arm study evaluated the efficacy and safety of first-line chemotherapy with carboplatin and dose-dense weekly paclitaxel plus bevacizumab (Avastin) in participants with epithelial ovarian, fallopian tube, or primary peritoneal cancer. Participants received 6-8 3-week cycles of treatment with bevacizumab 7.5 mg/kg intravenously (iv) on Day 1 of each cycle, paclitaxel 80 mg/m\^2 iv on days 1, 8, and 15 of each cycle, and carboplatin iv to an area under the curve (AUC) of 6 on day 1 of... Read More
This single arm study evaluated the efficacy and safety of first-line chemotherapy with carboplatin and dose-dense weekly paclitaxel plus bevacizumab (Avastin) in participants with epithelial ovarian, fallopian tube, or primary peritoneal cancer. Participants received 6-8 3-week cycles of treatment with bevacizumab 7.5 mg/kg intravenously (iv) on Day 1 of each cycle, paclitaxel 80 mg/m\^2 iv on days 1, 8, and 15 of each cycle, and carboplatin iv to an area under the curve (AUC) of 6 on day 1 of each cycle. Following combination chemotherapy, bevacizumab could be continued to be given as a monotherapy. Read Less
Gender:
FEMALE
Ages:
18 years and above
Trial Updated:
10/05/2017
Locations: Hospital Amaral Carvalho, Jau, SP +54 locations
Hospital Amaral Carvalho, Jau, SP
Hospital das Clinicas - FMUSP, Oncologia, Sao Paulo, SP
Centre Hospitalier Henri Duffaut; Hematologie, Avignon, Not set
Clinique Tivoli; Sce Radiotherapie, Bordeaux, Not set
Polyclinique Bordeaux Nord Aquitaine; Chimiotherapie Radiotherapie, Bordeaux, Not set
Ch De Brive La Gaillarde; Radiotherapie Oncologie, Brive La Gaillarde, Not set
Hopital Antoine Beclere; Service de Medecine Interne, Clamart, Not set
Centre Georges Francois Leclerc; Oncologie 3, Dijon, Not set
Chi Alpes Du Sud Site De Gap; Med Interne Et Polyvalente, GAP, Not set
Institut Daniel Hollard, Grenoble, Not set
Hôpital Saint Joseph; Oncologie Medicale, Marseille, Not set
CHRA;Hematologie, Metz Tessy, Not set
Centre Antoine Lacassagne; Hopital De Jour A2, Nice, Not set
GH Paris Saint Joseph; Hopital De Jour Oncologie, Paris, Not set
HOPITAL TENON; Cancerologie Medicale, Paris, Not set
Hopital De La Miletrie; Hematologie Et Oncologie Medicale, Poitiers, Not set
Institut de Cancerologie de La Loire; Radiotherapie, St Priest En Jarez, Not set
Centre Paul Strauss; Oncologie Medicale, Strasbourg, Not set
Institut Claudius Regaud; Departement Oncologie Medicale, Toulouse, Not set
Centre Alexis Vautrin; Oncologie Medicale, Vandoeuvre Les Nancy, Not set
IRCCS Istituto Nazionale Tumori Fondazione Pascale; Oncologia Medica B, Napoli, Campania
A.O. Universitaria Policlinico Di Modena; Oncologia, Modena, Emilia-Romagna
Universita' Cattolica Del Sacro Cuore; Reparto Ginecologia Oncologica, Roma, Lazio
Universita' Cattolica Del Sacro Cuore; Reparto Ginecologia Oncologica, Campobasso, Molise
Medisch Centrum Alkmaar, Alkmaar, Not set
Academisch Medisch Centrum; Inwendige Geneeskunde, Amsterdam, Not set
Medisch Spectrum Twente Enschede; Internal Medicine, Enschede, Not set
Academ Ziekenhuis Groningen; Medical Oncology, Groningen, Not set
Mc Haaglanden, Locatie Antoniushove; Interne Geneeskunde, Leidschendam, Not set
Sint Elizabeth Ziekenhuis; Inwendige Geneeskunde, Tilburg, Not set
Isala Klinieken, Locatie Sophia; Inwendige Geneeskunde, Zwolle, Not set
The Norvegian Radium Hospital Montebello; Dept of Oncology, Oslo, Not set
St. Olavs Hospital; Kvinneklinikken, Trondheim, Not set
Regional Clinical Oncology Dispensary, Krasnodar, Not set
Oncology Hospital; Chemotherapy Dept., Moscow, Not set
Russian Oncology Research Center n.a. N.N. Blokhin Dpt of Clinical Pharmacology and Chemotherapy, Moscow, Not set
City Clinical Oncology Hospital, Moscow, Not set
Medical Radiological Scientific Center; Department of Radiotherapy of Gynaecological Disease, Obninsk, Kaluzhskaya Region, Not set
St. Petersburg Oncology & Gynecology; City Clinical Oncology Dispensary, Saint-Petersburg, Not set
SBI of Healthcare of Stavropol region Stavropol Regional Clinical Oncology Dispensary, Stavropol, Not set
Hospital Univ Vall d'Hebron; Servicio de Oncologia, Barcelona, Not set
Hospital de la Santa Creu i Sant Pau; Servicio de Oncologia, Barcelona, Not set
Hospital General Universitario Gregorio Marañon; Servicio de Oncologia, Madrid, Not set
Centro Oncologico MD Anderson Internacional; Servicio de Oncologia, Madrid, Not set
Hospital Universitario Clínico San Carlos; Servicio de Oncologia, Madrid, Not set
Hospital Universitario La Paz; Servicio de Oncologia, Madrid, Not set
Hospital Clinico Universitario Virgen de la Victoria; Servicio de Oncologia, Malaga, Not set
Instituto Valenciano Oncologia; Oncologia Medica, Valencia, Not set
Hospital Clinico Universitario de Valencia; Servicio de Onco-hematologia, Valencia, Not set
Sahlgrenska Universitetssjukhuset; Onkology, Gothenburg, Not set
Uni Hospital Linkoeping; Dept. of Oncology, Linköping, Not set
Norrlands Uni Hospital; Onkologi Avd., Umea, Not set
Akademiska sjukhuset, Onkologkliniken, Uppsala, Not set
Örebro University Hospital; Department of Gynecologic Oncology, Örebro, Not set
Royal Marsden Hospital; Dept of Med-Onc, London, Not set
Conditions: Ovarian Cancer
Dose-finding Study in Platinum-Resistant Ovarian Cancer
Completed
* Dose-finding study of GSK2110183 administered in combination with carboplatin and paclitaxel to any subject with recurrent ovarian cancer.
* Safety and efficacy study of GSK2110183 administered in combination with carboplatin and paclitaxel to subjects with platinum-resistant ovarian cancer.
* Dose-finding study of GSK2110183 administered in combination with carboplatin and paclitaxel to any subject with recurrent ovarian cancer.
* Safety and efficacy study of GSK2110183 administered in combination with carboplatin and paclitaxel to subjects with platinum-resistant ovarian cancer. Read Less
Gender:
FEMALE
Ages:
18 years and above
Trial Updated:
08/30/2017
Locations: Royal Brisbane and Women's Hospital, Herston, Queensland +9 locations
Royal Brisbane and Women's Hospital, Herston, Queensland
Peter MacCallum Cancer Centre, East Melbourne, Victoria
Western Hospital, Footscray, Victoria
Royal Women's Hospital, Parkville, Victoria
Sir Charles Gairdner Hospital, Nedlands, Western Australia
Medical Radiology Scientific Center of Ministry of Healthcare and Social Development of RF, Omskaya, Not set
City Clinical Oncology Dispensary, Saint-Petersburg, Not set
Mount Vernon Cancer Center, Northwood, Middlesex, London
Royal Surrey County Hospital NHS Foundation Trust, Guildford, Surry
Imperial College Healthcare NHS Trust, London, Not set
Conditions: Recurrent Platinum-resistant Ovarian Cancer
A Study of Bevacizumab With Taxane Therapy in Participants With Triple Negative Breast Cancer
Completed
This open-label, multi-center study will evaluate the safety, tolerability and effect of bevacizumab (Avastin) in combination with taxane (paclitaxel/ docetaxel) monotherapy on disease progression, survival time and Karnofsky performance status in female participants with estrogen-, progesterone- and human epidermal growth factor receptor 2 (HER2)-negative (triple-negative) breast cancer.
This open-label, multi-center study will evaluate the safety, tolerability and effect of bevacizumab (Avastin) in combination with taxane (paclitaxel/ docetaxel) monotherapy on disease progression, survival time and Karnofsky performance status in female participants with estrogen-, progesterone- and human epidermal growth factor receptor 2 (HER2)-negative (triple-negative) breast cancer. Read Less
Gender:
FEMALE
Ages:
18 years and above
Trial Updated:
08/25/2017
Locations: Not set, Bangor, Not set +9 locations
Not set, Bangor, Not set
Not set, Cottingham, Not set
Not set, Exeter, Not set
Not set, Grimsby, Not set
Not set, Harrogate, Not set
Not set, Plymouth, Not set
Not set, Portsmouth, Not set
Not set, Preston, Not set
Not set, Somerset, Not set
Not set, Wolverhampton, Not set
Conditions: Breast Cancer
Study Of Lapatinib In Combination With Paclitaxel In The Treatment Of Newly Diagnosed Inflammatory Breast Cancer
Completed
This Study was designed to determine how effective and safe a new investigational drug, lapatinib, is in combination with paclitaxel in treating patients with newly diagnosed inflammatory breast cancer. Tumor tissue collected pre-treatment, following 14 days of treatment and at the time of surgical resection will be examined for pathologic response and biologic activity by IHC (immunohistochemistry) within the tumor. Treatment will consist of 14 days of lapatinib monotherapy followed by 12 weeks... Read More
This Study was designed to determine how effective and safe a new investigational drug, lapatinib, is in combination with paclitaxel in treating patients with newly diagnosed inflammatory breast cancer. Tumor tissue collected pre-treatment, following 14 days of treatment and at the time of surgical resection will be examined for pathologic response and biologic activity by IHC (immunohistochemistry) within the tumor. Treatment will consist of 14 days of lapatinib monotherapy followed by 12 weeks of combination therapy with lapatinib and paclitaxel. Blood samples for hematology and chemistry panels, MUGA/ECHO exams and physical exams will be performed throughout the study to monitor safety. Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
05/27/2017
Locations: GSK Investigational Site, Miami, Florida +24 locations
GSK Investigational Site, Miami, Florida
GSK Investigational Site, Chicago, Illinois
GSK Investigational Site, Zion, Illinois
GSK Investigational Site, Houston, Texas
GSK Investigational Site, Campbelltown, New South Wales
GSK Investigational Site, Liverpool, New South Wales
GSK Investigational Site, Randwick, New South Wales
GSK Investigational Site, South Brisbane, Queensland
GSK Investigational Site, Bedford Park, South Australia
GSK Investigational Site, Box Hill, Victoria
GSK Investigational Site, Ringwood East, Victoria
GSK Investigational Site, Toronto, Ontario
GSK Investigational Site, Bayonne, Not set
GSK Investigational Site, Lille Cedex, Not set
GSK Investigational Site, Paris cedex 13, Not set
GSK Investigational Site, Ramat Gan, Not set
GSK Investigational Site, Auckland, Not set
GSK Investigational Site, Barcelona, Not set
GSK Investigational Site, Girona, Not set
GSK Investigational Site, Valencia, Not set
GSK Investigational Site, Sfax, Not set
GSK Investigational Site, Sfax, Not set
GSK Investigational Site, Tunis, Not set
GSK Investigational Site, Tunis, Not set
GSK Investigational Site, London, Not set
Conditions: Neoplasms, Breast
Safety and Efficacy of Carboplatin/Paclitaxel and Carboplatin/Paclitaxel/Bevacizumab With and Without Pictilisib in Previously Untreated Advanced or Recurrent Non-small Cell Lung Cancer
Completed
This multicenter, randomized, double-blind, placebo-controlled trial will evaluate the efficacy and safety of carboplatin/paclitaxel and carboplatin/paclitaxel/bevacizumab with and without pictilisib in particpants with previously untreated advanced or recurrent non-small cell lung cancer (NSCLC). Particpants will be randomized to receive 4 cycles of carboplatin (C)/paclitaxel (P) and either pictilisib or placebo, with (participants with non-squamous NSCLC) or without (participants with squamous... Read More
This multicenter, randomized, double-blind, placebo-controlled trial will evaluate the efficacy and safety of carboplatin/paclitaxel and carboplatin/paclitaxel/bevacizumab with and without pictilisib in particpants with previously untreated advanced or recurrent non-small cell lung cancer (NSCLC). Particpants will be randomized to receive 4 cycles of carboplatin (C)/paclitaxel (P) and either pictilisib or placebo, with (participants with non-squamous NSCLC) or without (participants with squamous NSCLC) bevacizumab (B). Anticipated time on study treatment is until disease progression or intolerable toxicity occurs. Participants in placebo arms with disease progression may cross over to open-label active pictilisib. Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
04/21/2017
Locations: Alabama Oncology, Birmingham, Alabama +119 locations
Alabama Oncology, Birmingham, Alabama
Highlands Oncology Group, Rogers, Arkansas
cCare, Encinitas, California
Kaiser Permanente - Oakland, Oakland, California
Desert Hematology Oncology Group, Rancho Mirage, California
Kaiser Permanente - Roseville, Roseville, California
Kaiser Permanente Sacramento Medical Center, Sacramento, California
Southern CA Permanente Med Grp, San Diego, California
Kaiser Permanente, San Francisco, California
K. Permanente - Santa Clara, Santa Clara, California
Stockton Hema Onc Med Grp Inc, Stockton, California
Kaiser Permanente - Vallejo, Vallejo, California
K. Permanente - Walnut Creek, Walnut Creek, California
Hematology Oncology PC; Bennett Cancer Center, Stamford, Connecticut
Lynn Regional Cancer Center West, Boca Raton, Florida
Florida Cancer Specialists - Fort Myers (Colonial Center Dr), Fort Myers, Florida
Cancer Specialists; North Florida ;Jacksonville (AC Skinner Pkwy), Jacksonville, Florida
Advanced Medical Specialties, Miami, Florida
Florida Cancer Specialists (St. Petersburg - St. Anthony's Professional Building), Saint Petersburg, Florida
University Cancer & Blood Center, LLC, Athens, Georgia
Peachtree Hematology & Oncology Consultants, Pc, Atlanta, Georgia
Georgia Cancer Specialists, Atlanta, Georgia
Hematology-Oncology of Indiana, Pc, Indianapolis, Indiana
Franklin Square Hospital, Baltimore, Maryland
Massachusetts General Hospital., Boston, Massachusetts
Dana Farber Cancer Inst., Boston, Massachusetts
Beth Israel Deaconess Medical Center, Boston, Massachusetts
Wayne State University; Hemat/Onc, 4HW CRC, Detroit, Michigan
Nebraska Methodist Hospital, Omaha, Nebraska
Va Sierra Nevada Health Care System, Reno, Nevada
San Juan Oncology Associates, Farmington, New Mexico
Roswell Park Cancer Inst., Buffalo, New York
Piedmont Hematology Oncology Associates, Winston-Salem, North Carolina
Gabrail Cancer Center, Canton, Ohio
The Christ Hospital, Cincinnati, Ohio
Univ Hosp Case Medical Center, Cleveland, Ohio
Center for Biomedical Research LLC, Knoxville, Tennessee
The Sarah Cannon Research Inst, Nashville, Tennessee
Vanderbilt, Nashville, Tennessee
University of Texas M.D. Anderson Cancer Center, Houston, Texas
Wellmonth Physician Services, Bristol, Virginia
Blue Ridge Cancer Care - Roanoke, Roanoke, Virginia
VA Puget Sound Health Care Sys, Seattle, Washington
Northwest Medical Specialties, Tacoma, Washington
Clinica Universitaria Reina Fabiola, Cordoba, Not set
Instituto FIDES, La Plata, Not set
Isis Centro Especializado de Luces; Oncology, Santa Fe, Not set
Royal Prince Alfred Hospital; Sydney Cancer Centre, Camperdown, New South Wales
St Vincent'S Hospital, Darlinghurst, New South Wales
Calvary Mater Newcastle; Medical Oncology, Waratah, New South Wales
Flinders Medical Centre; Medical Oncology, Bedford Park, South Australia
Royal Hobart Hospital; Medical Oncology, Hobart, Tasmania
Footscray Hospital, Footscray, Victoria
Royal Melbourne Hospital; Hematology and Medical Oncology, Parkville, Victoria
Centro de Oncologia da Bahia - CENOB, Salvador, BA
Clinica de Tratamento e Pesquisa Oncologica - Oncotek, Brasilia, DF
Instituto Nacional de Cancer - INCa; Oncologia, Rio de Janeiro, RJ
Liga Norte Riograndense Contra O Câncer, Natal, RN
Santa Casa de Misericordia de Porto Alegre, Porto Alegre, RS
Hospital Mae de Deus, Porto Alegre, RS
Centro de Pesquisas Oncologicas - CEPON, Florianopolis, SC
Hospital Amaral Carvalho, Jau, SP
Instituto do Cancer do Estado de Sao Paulo - ICESP, Sao Paulo, SP
Instituto de Oncologia de Sorocaba - CEPOS, Sorocaba, SP
Mcgill University - Royal Victoria Hospital; Oncology, Montreal, Quebec
Hopital du Sacre-Coeur, Montreal, Quebec
Clinica Santa Maria, Santiago, Not set
Fundacion Arturo Lopez Perez, Santiago, Not set
Instituto Oncologico del sur, Temuco, Not set
Hospital Clinico Vina del Mar, Viña del Mar, Not set
Hopital Morvan, Brest, Not set
Clinique Victor Hugo; Radiotherapie, Le Mans, Not set
Clinique Catherine de Sienne; Service de cancérologie, Nantes, Not set
Ico Rene Gauducheau; Oncologie, Saint Herblain, Not set
Centre Hospitalier de Villefranche sur Saone, Villefranche-sur-Saone, Not set
Institut Gustave Roussy; Departement Oncologie Medicale, Villejuif, Not set
Zentralklinik Bad Berka GmbH; Abteilung Onkologie und Hämatologie, Bad Berka, Not set
Asklepios-Fachkliniken Muenchen-Gauting; Onkologie, Gauting, Not set
Krankenhaus Grosshansdorf;Pneumologie & Thoraxchirurgie, Grosshansdorf, Not set
St. Vincentius Kliniken Karlsruhe; Abteilung Hämatologie / Onkologie, Karlsruhe, Not set
Universitätsmedizin der Johannes Gutenberg-Universität Mainz, Medizinische Klinik, Pneumologie, Mainz, Not set
Universitätsklinikum Regensburg; Klinik und Poliklinik für Innere Medizin II, Pneumologie, Regensburg, Not set
Universitätsklinikum Ulm; Medizinische Uni-Klinik III Abt. Innere Medizin III Hämatologie u. Onkolo., Ulm, Not set
Schwarzwald-Baar Klinikum/VS GmbH; Onkologie/Hämatologie/Infektologie, Villingen-Schwenningen, Not set
Orszagos Koranyi TBC es Pulmonologiai Intezet, Budapest, Not set
Koch Robert Korhaz, Edeleny, Not set
Veszprem Megyei Onkormanyzat Tudogyogyintezet, Farkasgyepu, Not set
Vas Megyei Markusovszky Korhaz ; Pulmonology, Szombathely, Not set
Tudogyogyintezet Torokbalint, Torokbalint, Not set
Zala Megyei Korhaz; Dept of Pulmonary Medicine, Zalaegerszeg, Not set
Shaare Zedek Medical Center; Oncology Dept, Jerusalem, Not set
Meir Medical Center; Oncology, Kfar-Saba, Not set
Chaim Sheba Medical Center; Oncology Dept, Ramat Gan, Not set
Ausl Di Bologna-Ospedale Bellaria;U.O. Oncologia Medica, Bologna, Emilia-Romagna
Irccs Centro Di Riferimento Oncologico (CRO); Dipartimento Di Oncologia Medica, Aviano, Friuli-Venezia Giulia
ASST DI MONZA; Oncologia Medica, Monza, Lombardia
Az. Osp. S. Luigi Gonzaga; Malattie Apparato Respiratorio 5 Ad Indirizzo Oncologico, Orbassano, Piemonte
A.O.U.I. VERONA-OSPEDALE POLICLINICO G.B. ROSSI BORGO ROMA;ONCOLOGIA MEDICA-d.U., Verona, Veneto
Amphia Ziekenhuis, Breda, Not set
Catharina-ziekenhuis; Longgeneeskunde en Tuberculose, Eindhoven, Not set
Universitair Medisch Centrum Groningen, Groningen, Not set
Regional Oncology Center, Chelyabinsk, Not set
Moscow city oncology hospital #62 of Moscow Healthcare Department, Moscow, Not set
City Oncology Hospital; Chemotherapy Dept, Nizhny Novgorod, Not set
Leningrad Regional Clinical Hospital, St Petersburg, Not set
Rsrch Onc Inst of Rosmed Tech; n.a. prof. N.N. Petrov; Dept of Surgery, St. Petersburg, Not set
Hospital Nuestra Señora de Sonsoles; servicio de Oncologia, Avila, Not set
Hospital Univ Vall d'Hebron; Servicio de Oncologia, Barcelona, Not set
Hospital Universitari Germans Trias i Pujol; Servicio de Oncologia, Barcelona, Not set
Hospital Universitario 12 de Octubre; Servicio de Oncologia, Madrid, Not set
Hospital Universitario Puerta de Hierro; Servicio de Oncologia, Madrid, Not set
Kiev City Clinical Oncology Center, Kiev, Not set
Volyn Regional Oncology Dispensary, Lutsk, Not set
State Oncology Regional Treatment-Diagnostic Center; Chemotherapy Department, Lviv, Not set
Crimean Republican Institute; Oncology Clin Dispensary; Chemotherapy Dept, Simferopol, Not set
Sumy Reg. Clin. Oncological Dispensary; Thoracall Department, Sumy, Not set
Zaporizhzhia Regional Clinical Oncology Dispensary; Zaporizhzhya State Medical University, Zaporizhzhya, Not set
Royal Surrey County Hospital; St. Lukes Cancer Centre, Guildford, Not set
Leicester Royal Infirmary; Dept. of Medical Oncology, Leicester, Not set
Christie Hospital Nhs Trust; Medical Oncology, Manchester, Not set
Conditions: Non-Small Cell Lung Cancer
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