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Cisplatin Treatment Options in United Kingdom
A collection of 298 research studies where Cisplatin is the interventional treatment. These studies are located in the United Kingdom . Cisplatin is used for conditions such as Head and Neck Cancer, Lung Cancer and Non-Small Cell Lung Cancer.
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Phase III Open Label Study of MEDI 4736 With/Without Tremelimumab Versus Standard of Care (SOC) in Recurrent/Metastatic Head and Neck Cancer
Completed
This is a randomized, open-label, multi-center, 3-arm, global Phase III study to determine the efficacy and safety of MEDI4736 + tremelimumab combination or MEDI4736 monotherapy versus SoC (EXTREME regimen) in the treatment of patients with SCCHN who have not received prior systemic chemotherapy for recurrent or metastatic disease.
This is a randomized, open-label, multi-center, 3-arm, global Phase III study to determine the efficacy and safety of MEDI4736 + tremelimumab combination or MEDI4736 monotherapy versus SoC (EXTREME regimen) in the treatment of patients with SCCHN who have not received prior systemic chemotherapy for recurrent or metastatic disease. Read Less
Gender:
ALL
Ages:
Between 18 years and 130 years
Trial Updated:
09/16/2021
Locations: Research Site, Aurora, Colorado +196 locations
Research Site, Aurora, Colorado
Research Site, Washington, District of Columbia
Research Site, Fort Myers, Florida
Research Site, Saint Petersburg, Florida
Research Site, Tampa, Florida
Research Site, Atlanta, Georgia
Research Site, Chicago, Illinois
Research Site, Baltimore, Maryland
Research Site, Baltimore, Maryland
Research Site, Boston, Massachusetts
Research Site, Morristown, New Jersey
Research Site, New York, New York
Research Site, New York, New York
Research Site, Chapel Hill, North Carolina
Research Site, Charlotte, North Carolina
Research Site, Winston-Salem, North Carolina
Research Site, Cleveland, Ohio
Research Site, Columbus, Ohio
Research Site, Nashville, Tennessee
Research Site, Graz, Not set
Research Site, Innsbruck, Not set
Research Site, Linz, Not set
Research Site, Wien, Not set
Research Site, Brussels, Not set
Research Site, Brussels, Not set
Research Site, Bruxelles, Not set
Research Site, Leuven, Not set
Research Site, Namur, Not set
Research Site, Barretos, Not set
Research Site, Curitiba, Not set
Research Site, Florianópolis, Not set
Research Site, Ijui, Not set
Research Site, Porto Alegre, Not set
Research Site, Porto Alegre, Not set
Research Site, Porto Alegre, Not set
Research Site, Recife, Not set
Research Site, Rio de Janeiro, Not set
Research Site, Santo Andre, Not set
Research Site, Santo André, Not set
Research Site, São José do Rio Preto, Not set
Research Site, São Paulo, Not set
Research Site, Calgary, Alberta
Research Site, Winnipeg, Manitoba
Research Site, Moncton, New Brunswick
Research Site, Halifax, Nova Scotia
Research Site, Hamilton, Ontario
Research Site, London, Ontario
Research Site, Ottawa, Ontario
Research Site, Toronto, Ontario
Research Site, Montreal, Quebec
Research Site, Bordeaux, Not set
Research Site, Brest, Not set
Research Site, Dijon, Not set
Research Site, Lyon Cedex 08, Not set
Research Site, Nice, Not set
Research Site, Paris, Not set
Research Site, Poitiers Cedex, Not set
Research Site, Toulouse Cedex, Not set
Research Site, Vandoeuvre les Nancy, Not set
Research Site, Villejuif, Not set
Research Site, Berlin, Not set
Research Site, Erlangen, Not set
Research Site, Essen, Not set
Research Site, Frankfurt am Main, Not set
Research Site, Freiburg, Not set
Research Site, Hamburg, Not set
Research Site, Heidelberg, Not set
Research Site, Mainz, Not set
Research Site, Tübingen, Not set
Research Site, Würzburg, Not set
Research Site, Athens, Not set
Research Site, Athens, Not set
Research Site, Athens, Not set
Research Site, Athens, Not set
Research Site, Heraklion, Not set
Research Site, Thessaloniki, Not set
Research Site, Bangalore, Not set
Research Site, Bangalore, Not set
Research Site, Bengaluru, Not set
Research Site, Gurgaon, Not set
Research Site, Karamsad, Not set
Research Site, Madurai, Not set
Research Site, Pune, Not set
Research Site, Cona, Not set
Research Site, Firenze, Not set
Research Site, Messina, Not set
Research Site, Milano, Not set
Research Site, Padova, Not set
Research Site, Palermo, Not set
Research Site, Salerno, Not set
Research Site, Siena, Not set
Research Site, Torino, Not set
Research Site, Akashi-shi, Not set
Research Site, Chiba-shi, Not set
Research Site, Fukuoka-shi, Not set
Research Site, Hirakata-shi, Not set
Research Site, Isehara-shi, Not set
Research Site, Kagoshima-shi, Not set
Research Site, Kanazawa-shi, Not set
Research Site, Kitaadachi-gun, Not set
Research Site, Kobe-shi, Not set
Research Site, Koto-ku, Not set
Research Site, Natori-shi, Not set
Research Site, Okayama-shi, Not set
Research Site, Osaka-shi, Not set
Research Site, Osakasayama, Not set
Research Site, Sapporo-shi, Not set
Research Site, Sapporo, Not set
Research Site, Sunto-gun, Not set
Research Site, Takatsuki-shi, Not set
Research Site, Toyoake-shi, Not set
Research Site, Yokohama-shi, Not set
Research Site, Cheongju-si, Not set
Research Site, Hwasun-gun, Not set
Research Site, Incheon, Not set
Research Site, Seo-Gu, Not set
Research Site, Seongnam-si, Not set
Research Site, Seoul, Not set
Research Site, Seoul, Not set
Research Site, Seoul, Not set
Research Site, Seoul, Not set
Research Site, Suwon-si, Not set
Research Site, Cebu City, Not set
Research Site, Las Pinas, Not set
Research Site, Quezon City, Not set
Research Site, Białystok, Not set
Research Site, Bielsko-Biała, Not set
Research Site, Gdańsk, Not set
Research Site, Gdynia, Not set
Research Site, Lublin, Not set
Research Site, Poznan, Not set
Research Site, Poznan, Not set
Research Site, Szczecin, Not set
Research Site, Warszawa, Not set
Research Site, Łódź, Not set
Research Site, Suceava, Not set
Research Site, Arkhangelsk, Not set
Research Site, Ekaterinburg, Not set
Research Site, Krasnodar, Not set
Research Site, Moscow, Not set
Research Site, Obninsk, Not set
Research Site, Omsk, Not set
Research Site, Saint Petersburg, Not set
Research Site, Saint Petersburg, Not set
Research Site, Saint-Petersburg, Not set
Research Site, Sochi, Not set
Research Site, St.Petersburg, Not set
Research Site, Ufa, Not set
Research Site, Bratislava, Not set
Research Site, Kosice, Not set
Research Site, Badajoz, Not set
Research Site, Barcelona, Not set
Research Site, Barcelona, Not set
Research Site, Jaén, Not set
Research Site, L'Hospitalet de Llobregat, Not set
Research Site, Madrid, Not set
Research Site, Madrid, Not set
Research Site, Madrid, Not set
Research Site, Madrid, Not set
Research Site, Marbella, Not set
Research Site, Málaga, Not set
Research Site, Valencia, Not set
Research Site, Zaragoza, Not set
Research Site, Kaohsiung, Not set
Research Site, Taichung, Not set
Research Site, Taichung, Not set
Research Site, Tainan, Not set
Research Site, Taipei, Not set
Research Site, Taipei, Not set
Research Site, Taipei, Not set
Research Site, Bangkok, Not set
Research Site, Bangkok, Not set
Research Site, Chiang Mai, Not set
Research Site, Hat Yai, Not set
Research Site, Pathumthani, Not set
Research Site, Dnipro, Not set
Research Site, Ivano-Frankivsk, Not set
Research Site, Kapitanivka Village, Not set
Research Site, Kharkiv Region, Not set
Research Site, Kirovohrad, Not set
Research Site, Kryvyi Rih, Not set
Research Site, Kyiv, Not set
Research Site, Kyiv, Not set
Research Site, Odesa, Not set
Research Site, Sumy, Not set
Research Site, Vinnytsia, Not set
Research Site, Bebington, Not set
Research Site, Birmingham, Not set
Research Site, London, Not set
Research Site, London, Not set
Research Site, Manchester, Not set
Research Site, Sutton, Not set
Research Site, Taunton, Not set
Research Site, Ha Noi, Not set
Research Site, Hanoi, Not set
Research Site, Hanoi, Not set
Research Site, Ho Chi Minh city, Not set
Conditions: Squamous Cell Carcinoma of the Head and Neck
A Study of Ramucirumab (LY3009806) in Combination With Capecitabine and Cisplatin in Participants With Stomach Cancer
Completed
The main purpose of this study is to evaluate the efficacy of ramucirumab, which is a targeted antibody, in combination with capecitabine and cisplatin compared to capecitabine and cisplatin alone in participants with stomach cancer.
The main purpose of this study is to evaluate the efficacy of ramucirumab, which is a targeted antibody, in combination with capecitabine and cisplatin compared to capecitabine and cisplatin alone in participants with stomach cancer. Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
07/29/2021
Locations: Highlands Oncology Group, Fayetteville, Arkansas +134 locations
Highlands Oncology Group, Fayetteville, Arkansas
Comprehensive Blood and Cancer Center, Bakersfield, California
St Jude Medical Center, Fullerton, California
SMO TRIO -Translational Research, Los Angeles, California
UCLA Medical Center, Los Angeles, California
Cancer Care Associates Medical Group, Redondo Beach, California
Coastal Integrative Cancer Care, San Luis Obispo, California
Central Coast Medical Oncology Corporation, Santa Monica, California
University of Colorado School of Medicine, Aurora, Colorado
Yale University School of Medicine, New Haven, Connecticut
Holy Cross Hospital Inc., Fort Lauderdale, Florida
Florida Cancer Specialists, Fort Myers, Florida
Florida Cancer Specialists and Research Institute, Saint Petersburg, Florida
Emory University, Atlanta, Georgia
Illinois CancerCare, Peoria, Illinois
Dana Farber Cancer Institute, Boston, Massachusetts
Weill Cornell Medical College, New York, New York
Memorial Sloan Kettering Cancer Center, New York, New York
Oncology Hematology Care Inc, Cincinnati, Ohio
Fox Chase Cancer Center, Philadelphia, Pennsylvania
Allegheny General Hospital, Pittsburgh, Pennsylvania
SMO Sarah Cannon Research Inst., Nashville, Tennessee
Tennessee Oncology PLLC, Nashville, Tennessee
UT Southwestern Med Ctr, Dallas, Texas
Baylor College of Medicine, Houston, 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., Viedma, Rio Negro
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., Rosario, Santa Fe
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., Ciudad Autonoma Buenos Aires, 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., La Rioja, 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., Rosario, 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., Salta, 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., Charleroi, 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., Gent, 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 1-888-545-5972 Mon - Fri, 9 AM to 4 PM or 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri, 9 AM to 5 PM Eastern Time or speak with your personal physician., Montreal, Not set
For additional information regarding investigative sites for this trial, contact 1-888-545-5972 Mon - Fri, 9 AM to 4 PM or 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri, 9 AM to 5 PM Eastern Time or speak with your personal physician., Montreal, Not set
For additional information regarding investigative sites for this trial, contact 1-888-545-5972 Mon - Fri, 9 AM to 4 PM or 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri, 9 AM to 5 PM Eastern Time or speak with your personal physician., Ottawa, Not set
For additional information regarding investigative sites for this trial, contact 1-888-545-5972 Mon - Fri, 9 AM to 4 PM or 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri, 9 AM to 5 PM Eastern Time or speak with your personal physician., Toronto, Not set
For additional information regarding investigative sites for this trial, contact 1-888-545-5972 Mon - Fri, 9 AM to 4 PM or 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri, 9 AM to 5 PM Eastern Time or speak with your personal physician., Toronto, Not set
For additional information regarding investigative sites for this trial, contact 1-888-545-5972 Mon - Fri, 9 AM to 4 PM or 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri, 9 AM to 5 PM Eastern Time or speak with your personal physician., Toronto, Not set
For additional information regarding investigative sites for this trial, contact 1-888-545-5972 Mon - Fri, 9 AM to 4 PM or 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri, 9 AM to 5 PM Eastern Time or speak with your personal physician., Toronto, Not set
For additional information regarding investigative sites for this trial, contact 1-888-545-5972 Mon - Fri, 9 AM to 4 PM or 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri, 9 AM to 5 PM Eastern Time or speak with your personal physician., Vancouver, 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., Brno, 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., Hradec Kralove, 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., Olomouc, 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., Praha 2, 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., Praha 5, 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., Aalborg, 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., Aarhus C, 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., Odense C, 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., Helsinki, 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., Oulu, 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., Avignon Cedex 9, 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., Clermont-Ferrand, 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., Lille, 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., Saint Etienne, 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., Saint Herblain Cedex, 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., Dresden, 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., Frankfurt am Main, 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., Hamburg, 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., Mannheim, 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., München, 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., Budapest, 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., Debrecen, 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., Gyula, 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., Kaposvar, 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., Szolnok, 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., Haifa, 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., Petach Tikva, 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 Jaffa, 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., Firenze, 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., Pisa, 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., Roma, 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., Torrette Di Ancona, 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., Udine, 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., Chiba, 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., Fukuoka, 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., Higashinari-Ku, 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., Kashiwa, 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., Kitaadachi-Gun, 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., Kobe, 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., Koto-ku, 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., Nagoya, 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., Osaka, 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., Suita-shi, 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., Sunto-Gun, 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., Utsunomiya, 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., Mexico City, DF
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., Guadalajara, Jalisco
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 Bernardino, Toluca
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., Juchitan, 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., Merida, 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., Mexico City, 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., Mexico, 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., Oaxaca, 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., Amsterdam, 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., Amsterdam, 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., Breda, 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., Nieuwegein, 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., Sittard - Geleen, 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., Lodz, 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., Warszawa, Not set
Ad-Vance Medical Research, Ponce, Not set
Hospital Espanol Auxilio Mutuo, San Juan, Not set
VA Caribbean Healthcare System, San Juan, Not set
Hospital Municipal de San Juan, San Juan, 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., Arkhangelsk, 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., Moscow, 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., Saint Petersburg, 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., Saint Petersburg, 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., Saint Petersburg, 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., 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., Elche, 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., 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., Aberdeen, 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, 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., London, 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., Manchester, 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., Merseyside, 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., Nottingham, 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., Sheffield, 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., Sutton, Not set
Conditions: Metastatic Gastric Adenocarcinoma, Gastroesophageal Junction Adenocarcinoma
Study Comparing Veliparib Plus Carboplatin and Paclitaxel Versus Investigator's Choice of Standard Chemotherapy in Adults Receiving First Cytotoxic Chemotherapy for Metastatic or Advanced Non-Squamous Non-Small Cell Lung Cancer (NSCLC) and Who Are Current or Former Smokers
Completed
The purpose of this study is to evaluate the safety and efficacy of veliparib plus carboplatin and paclitaxel versus the Investigator's choice of standard chemotherapy in adults with metastatic or advanced non-squamous non-small cell lung cancer.
The purpose of this study is to evaluate the safety and efficacy of veliparib plus carboplatin and paclitaxel versus the Investigator's choice of standard chemotherapy in adults with metastatic or advanced non-squamous non-small cell lung cancer. Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
02/08/2021
Locations: Clearview Cancer Institute /ID# 131434, Huntsville, Alabama +139 locations
Clearview Cancer Institute /ID# 131434, Huntsville, Alabama
University of South Alabama /ID# 131518, Mobile, Alabama
Highlands Oncology Group /ID# 131250, Springdale, Arkansas
CBCC Global Research, Inc. at /ID# 132709, Bakersfield, California
California Cancer Assoc. R&E /ID# 131392, Encinitas, California
California Cancer Assoc. R&E /ID# 131949, Encinitas, California
LA Hem-Oncology Med Group /ID# 131639, Los Angeles, California
St Jude Hospital dba St Joseph /ID# 132943, Santa Rosa, California
Icri /Id# 132942, Whittier, California
University of Florida - Archer /ID# 132408, Gainesville, Florida
NorthShore University HealthSystem - Evanston Hospital /ID# 130200, Evanston, Illinois
Goshen Center for Cancer Care /ID# 130216, Goshen, Indiana
University of Louisville /ID# 130217, Louisville, Kentucky
Cancer Center of Acadiana /ID# 133611, Lafayette, Louisiana
Henry Ford Health System /ID# 130234, Detroit, Michigan
Herbert Herman Cancer Center /ID# 130239, Lansing, Michigan
Washington University-School of Medicine /ID# 131651, Saint Louis, Missouri
MD Anderson Cancer Center at Cooper - Camden /ID# 131490, Camden, New Jersey
Gabrail Cancer Center Research /ID# 130205, Canton, Ohio
Univ Oklahoma HSC /ID# 132888, Oklahoma City, Oklahoma
Albert Einstein Medical Center /ID# 134498, Philadelphia, Pennsylvania
Allegheny General Hospital /ID# 134049, Pittsburgh, Pennsylvania
The Jones Clinic, PC /ID# 130215, Germantown, Tennessee
UT Southwestern Medical Center /ID# 130236, Dallas, Texas
Univ Texas HSC San Antonio /ID# 132972, San Antonio, Texas
Coiba /Id# 132153, Berazategui, Buenos Aires, Not set
Centro Investigacion Pergamino /ID# 132152, Pergamino, Not set
Hospital Britanico /ID# 134874, Rosario, Santa FE, Not set
Instituto de Oncologia de Rosa /ID# 132150, Rosario, Santa FE, Not set
St George Hospital /ID# 132481, Kogarah, New South Wales
Southern Medical Day Care Ctr /ID# 132482, Wollongong, New South Wales
Flinders Centre for Innovation /ID# 134288, Bedford Park, South Australia
Royal Hobart Hospital /ID# 132477, Hobart, Tasmania
Qe Ii Hsc /Id# 133408, Halifax, Nova Scotia
Victoria Hospital /ID# 132161, London, Ontario
Windsor Regional Hospital /ID# 135989, Windsor, Ontario
CSSS Alphonse-Desjardins, CHAU de Levis /ID# 132155, Quebec City, Quebec
Krajska nemocnice Liberec a.s. /ID# 132694, Liberec, Not set
Univ Hosp Ostrava-Poruba /ID# 132690, Ostrava, Not set
Multiscan s.r.o. /ID# 132689, Pardubice, Not set
Vseobecna Fakultni Nemocnice /ID# 135118, Prague, Not set
Odense Universitets Hospital /ID# 131912, Odense C, Syddanmark
Satakunnan Sairaanhoitopiiri /ID# 133632, Pori, Not set
Vaasa Central Hospital /ID# 131930, Vaasa, Not set
Charite-Univ. Berlin, Benjamin-Franklin /ID# 131927, Berlin, Not set
Lungen Clinic Grosshansdorf /ID# 131928, Grosshansdorf, Not set
Univ Klinik Eppendorf Hamburg /ID# 131926, Hamburg, Not set
Klinik Loewenstein GmbH /ID# 131925, Löwenstein, Not set
CRU Hungary Egeszsegugyi és Szolgaltato Kft. /ID# 133441, Miskolc, Borsod-Abauj-Zemplen
Orszagos Koranyi Pulmonologiai Intezet /ID# 132738, Budapest XII, Budapest
Debreceni Egyetem Klinikai Kozpont /ID# 132742, Debrecen, Not set
Koch Robert Hospital /ID# 133440, Edelény, Not set
Veszprem Megyei Tudogyogyintez /ID# 132739, Farkasgyepu, Not set
Petz Aladar Megyei Oktato Korh /ID# 132741, Gyor, Not set
Matrahaza Gyogyintezet /ID# 132743, Kékesteto, Not set
Assaf Harofeh Medical Center /ID# 132830, Be'er Ya'akov, Not set
Shaare Zedek Medical Center /ID# 132834, Jerusalem, Not set
Meir Medical Center /ID# 132832, Kfar Saba, Not set
Sheba Medical Center /ID# 132833, Ramat Gan, Not set
Aichi Cancer Center Hospital /ID# 134129, Nagoya-shi, Aichi
Kurume University Hospital /ID# 134117, Kurume-shi, Fukuoka
Hokkaido University Hospital /ID# 134123, Sapporo-shi, Hokkaido
Kanagawa Cardiovascular and Respiratory Center /ID# 134127, Yokohama-shi, Kanagawa
Sendai Kousei Hospital /ID# 135491, Sendai-shi, Miyagi
Kindai University Hospital /ID# 134112, Osaka-sayama-shi, Osaka
Osaka City General Hospital /ID# 134115, Osaka-shi, Osaka
National Cancer Center Hospital /ID# 135129, Chuo-ku, Tokyo
The Cancer Institute Hospital Of JFCR /ID# 135492, Koto-ku, Tokyo
Yamaguchi - Ube Medical Center /ID# 135284, Ube-shi, Yamaguchi
Hiroshima Citizens Hospital /ID# 135130, Hiroshima, Not set
Kishiwada City Hospital /ID# 136548, Kishiwada, Not set
Dong-A University Hospital /ID# 131609, Busan, Busan Gwang Yeogsi
Seoul National Univ Bundang ho /ID# 131610, Seongnam, Gyeonggido
Inha University Hospital /ID# 147924, Jung-gu, Incheon Gwang Yeogsi
Chonnam National University Hospital /ID# 131612, Gwangju, Jeonranamdo
Samsung Medical Center /ID# 132471, Seoul, Seoul Teugbyeolsi
Chungbuk National Univ Hosp /ID# 131611, Cheongju, Not set
Vrije Universiteit Medisch Centrum /ID# 131967, Amsterdam, Not set
Catharina Ziekenhuis /ID# 131966, Eindhoven, Not set
Ziekenhuis St. Jansdal /ID# 131965, Harderwijk, Not set
St. Antonius Ziekenhuis /ID# 133635, Nieuwegein, Not set
Jeroen Bosch Ziekenhuis /ID# 131968, S Hertogenbosch, Not set
Canterbury District Health Boa /ID# 132469, Christchurch, Not set
Wellington Hospital (Capital and Coast District Health Board) /ID# 132470, Wellington, Not set
Federal State Budgetary Scientific Institution N.N. Blokhin Russian Cancer Resea /ID# 137085, Moscow, Moskva
Sverdlovsk Regional Oncology Center Dispensary /ID# 132375, Ekaterinburg, Sverdlovskaya Oblast
archangel Clinical Oncology /ID# 132376, Arkhangelsk, Not set
Moscow Regional Onc Dispensary /ID# 132381, Balashikha, Not set
Belgorod Oncology Dispensary /ID# 142638, Belgorod, Not set
Moscow Res Onc Inst Hertsen /ID# 132370, Moscow, Not set
State Regional Budgetary Healthcare Institution " Murmansk Regional Oncology Dis /ID# 137087, Murmansk, Not set
Orenburg Regional Clinical Onc /ID# 132371, Orenburg, Not set
Strategic medical systems LLC /ID# 206383, Sankt-Peterburg, Not set
Ogarev Mordovia State Univ /ID# 132377, Saransk, Not set
LLC BioEq Ltd. /ID# 132372, St. Petersburg, Not set
N.N. Petrov Research Inst Onc /ID# 137084, St. Petersburg, Not set
GVI Oncology /ID# 133268, Port Elizabeth, Eastern Cape
Dr Albert, Bouwer and Jordaan Incorporated /ID# 131775, Pretoria, Gauteng
Mary Potter Oncology Centre /ID# 131776, Pretoria, Gauteng
The Oncology Centre /ID# 131773, Durban, Kwazulu-Natal
Netcare Oncology Intervent Ctr /ID# 131777, Cape Town, Western Cape
Cape Town Oncology Trials /ID# 132734, Cape Town, Western Cape
GVI Rondebosch Oncology Centre /ID# 132732, Cape Town, Western Cape
Sandton Oncology Medical Group /ID# 131774, Johannesburg, Not set
Hospital Duran i Reynals /ID# 132879, L'Hospitalet de Llobregat, Barcelona
Hospital Universitario Fundacion Alcorcon /ID# 132909, Alcorcon, Not set
Hospital General Universitario Alicante /ID# 132881, Alicante, Not set
Hospital Universitario Dexeus - Grupo Quironsalud /ID# 132876, Barcelona, Not set
Hospital Universitario Vall d'Hebron /ID# 132871, Barcelona, Not set
MD Anderson Madrid /ID# 132905, Madrid, Not set
Hospital Universitario La Paz /ID# 132870, Madrid, Not set
Hospital Universitario HM Sanchinarro /ID# 132869, Madrid, Not set
Hospital Clinico Universitario de Valencia /ID# 132873, Valencia, Not set
China Medical University Hosp /ID# 131870, Taichung City, Taichung
Dalin Tzu Chi General Hospital /ID# 131872, Dalin Township, Not set
Taipei Medical University Hospital /ID# 133817, Taipei City, Not set
Taipei Veterans General Hosp /ID# 131871, Taipei City, Not set
Hacettepe University Medical Faculty /ID# 131913, Ankara, Not set
Ankara Univ Medical Faculty /ID# 131914, Ankara, Not set
Uludag University Medical Faculty /ID# 131915, Bursa, Not set
Dicle Universitesi Tip /ID# 136570, Diyarbakir, Not set
Gaziantep Universitesi Med /ID# 131917, Gaziantep, Not set
Dr. Suat Seren Gogus Has /ID# 136568, Izmir, Not set
Inonu University /ID# 136569, Malatya, Not set
Leicester Royal Infirmary /ID# 133930, Leicester, England
Cheltenham General Hospital /ID# 131951, Cheltenham, Gloucestershire
Norfolk and Norwich Univ Hosp /ID# 131953, Norwich, Norfolk
Royal United Hospitals Bath /ID# 132851, Bath, Not set
Belfast City Hospital /ID# 132858, Belfast, Not set
Heart of England NHS Foundation Trust /ID# 132855, Birmingham, Not set
Royal Blackburn Hospital /ID# 132853, Blackburn, Not set
Colchester General Hospital /ID# 133929, Colchester, Not set
Castle Hill Hospital /ID# 135489, Cottingham, Not set
Scunthorpe General Hospital /ID# 133931, Doncaster, Not set
James Paget University Hosp /ID# 131954, Great Yarmouth, Not set
Royal Gwent Hospital /ID# 133935, Gwent, Not set
Huddersfield Royal Infirmary /ID# 132854, Huddersfield, Not set
Charing Cross Hospital /ID# 131959, London, Not set
The Newcastle Upon Tyne Hospitals NHS Foundation Trust Freeman Hospital /ID# 131661, Newcastle Upon Tyne, Not set
York Hospital /ID# 132859, York, Not set
Conditions: Non-squamous Non-small Cell Lung Cancer
Bristol Bladder Trial
Unknown
26 patients with invasive primary transitional cell carcinoma of the bladder will receive 4 cycles of combination chemotherapy consisting of Cabazitaxel and Cisplatin both given intravenously on day 1 of each 3 weekly cycle prior to radical cystectomy, to evaluate the overall response rate and to determine whether this approach warrants further research of a phase II/III study.Participation in 2 sub studies will also be offered to the participants.
1. Contrast Magnetic resonance imaging (MRI )... Read More
26 patients with invasive primary transitional cell carcinoma of the bladder will receive 4 cycles of combination chemotherapy consisting of Cabazitaxel and Cisplatin both given intravenously on day 1 of each 3 weekly cycle prior to radical cystectomy, to evaluate the overall response rate and to determine whether this approach warrants further research of a phase II/III study.Participation in 2 sub studies will also be offered to the participants.
1. Contrast Magnetic resonance imaging (MRI ) scans will be taken at baseline and after cycle 1 and cycle 3.
2. A pilot sub study involving the circulating tumour cell concentration from blood samples taken at baseline, prior to each cycle of chemotherapy and prior to surgery Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
11/11/2020
Locations: Bristol Haematology + Oncology Centre, Horfield Road, Bristol, Not set
Bristol Haematology + Oncology Centre, Horfield Road, Bristol, Not set
Conditions: Infiltrating Bladder Urothelial Carcinoma
High Risk Neuroblastoma Study 1.8 of SIOP-Europe (SIOPEN)
Recruiting
This is a randomized study of the European SIOP Neuroblastoma Group (SIOPEN) in high-risk neuroblastoma (stages 2, 3, 4 and 4s MYCN-amplified neuroblastoma, stage 4 MYCN non amplified \> 12 months at diagnosis).
The protocol consists of a rapid, dose intensive induction chemotherapy, peripheral blood stem cell harvest, attempted complete excision of the primary tumour, myeloablative therapy followed by peripheral blood stem cell rescue, radiotherapy to the site of the primary tumour and immunot... Read More
This is a randomized study of the European SIOP Neuroblastoma Group (SIOPEN) in high-risk neuroblastoma (stages 2, 3, 4 and 4s MYCN-amplified neuroblastoma, stage 4 MYCN non amplified \> 12 months at diagnosis).
The protocol consists of a rapid, dose intensive induction chemotherapy, peripheral blood stem cell harvest, attempted complete excision of the primary tumour, myeloablative therapy followed by peripheral blood stem cell rescue, radiotherapy to the site of the primary tumour and immunotherapy (R4 randomization - isotretinoin and ch14.18/CHO (Dinutuximab beta, Qarziba ®).), with or without s.c. aldesleukin (IL-2)). Patients diagnosed after the closure of R3 randomization will not be R4 randomized. For these patients the use of ch14.18/CHO antibody is recommended without scIL-2 as continuous infusion as standard of care outside of controlled trials. ch14.18/CHO received marketing authorization by EMA in May 2017 (Qarziba ®).
In the induction phase, all patients receive Rapid COJEC following the result of the R3 randomization which was closed on June 8th, 2017 after inclusion of 630 patients as planned.
Following induction treatment peripheral blood stem cell harvest (PBSCH) is performed and complete excision of the primary tumour will be attempted.
Patients with an inadequate metastatic response to allow BuMel MAT followed by PBSCR at the end of induction should receive 2 TVD (Topotecan, Vincristine, Doxorubicin) cycles.
After Rapid COJEC induction, localized patients will proceed to consolidation. Patients aged 12-18 months at diagnosis, with stage 4 neuroblastoma, no MYCN amplification and without segmental chromosomal alterations (SCAs) are thought to have a good prognosis and will stop treatment after induction therapy and surgery to the primary tumour.
Consolidation consists of BuMel MAT based on the results of the R1 randomization followed by peripheral blood stem cell rescue (PBSCR) and radiotherapy to the site of the primary tumour.
The R2 immunotherapy randomization using ch14.18/CHO as 8 hour infusion on 5 consecutive days ( total dose (100mg/m²) with or without aldesleukin (IL-2) alternated with isotretinoin (13-cis-RA) is closed.
The amended R4 immunotherapy randomization using ch14.18/CHO as continuous infusion (total dose 100mg/m² over 10 days) with or without aldesleukin (IL-2) alternated with isotretinoin (13-cis-RA) has accrued according to plan with results pending awaiting data maturity and DMC approval. Read Less
Gender:
ALL
Ages:
Between 1 month and 21 years
Trial Updated:
10/21/2020
Locations: Women and Children´s Hospital, Adelaide, Not set +125 locations
Women and Children´s Hospital, Adelaide, Not set
Lady Cilento Children´s Hospital, Brisbane, Not set
John Hunter Children's Hospital, Newcastle, Not set
Royal Children's Hospital Melbourne, Parkville, Not set
Sydney Children's Hospital, Sydney, Not set
Children´s Hospital Westmead, Westmead, Not set
St. Anna Kinderspital, Vienna, Austra
Univ.-Klinik für Kinder- und Jugendheilkunde Graz, Graz, Not set
Univ.Klinik f. Kinder-u. Jugendheilkunde Innsbruck, Innsbruck, Not set
Landes- Kinderklinik Linz, Linz, Not set
St. Johanns Spital LKH Salzburg, Salzburg, Not set
Cliniques universitaires St-Luc, Brussels, Not set
Hôpital des Enfants, Brussels, Not set
University Hospital Gent, Gent, Not set
UZ Gasthuisberg, Leuven, Not set
CHR Citadelle, Lüttich, Not set
Clinique de l'Espérance, Montegnee, Not set
University Hospital Motol, Prague, Not set
Aarhus Universitetshospital, Aarhus, Not set
National State Hospital, Copenhagen, Not set
University Hospital of Odense, Odense, Not set
Skejby Hospital, Skejby, Not set
Hopital d'Enfants Dijon, Dijon, Not set
CHU de Grenoble, Grenoble, Not set
CHR Pellegrin, Le Pellerin, Not set
Centre Oscar Lambret de Lille, Lille, Not set
Hopitaux de Marseille La Timone, Marseille, Not set
CHR de Nantes, Nantes, Not set
Hôpital Trousseau Paris, Paris, Not set
Institut Curie, Paris, Not set
Hôpital American Memorial Hospital, Reims, Not set
CHU-Saint Etienne, Saint Etienne, Not set
Hôpital de Hautepierre, Strasbourg, Not set
Hôpital D'Enfants de Toulouse, Toulouse, Not set
Institut Gustave Roussy, Villejuif, Not set
"A&P Kyriakou" Children's Hospital, Athens, Not set
Aghia Sophia Children's Hospital, Athens, Not set
MITERA Hospital, Heraklion, Not set
PEPAGNH University Hospital, Heraklion, Not set
Madarász Children Hospital Budapest, Budapest, Not set
Semmelweis University of Budapest, Budapest, Not set
University of Debrecen, Debrecen, Not set
University of Pecs, Pécs, Not set
University of Szeged, Szeged, Not set
Dublin: OLHSC, Dublin, Not set
Rambam Medical Centre, Haifa, Not set
Schneider Children's Medical Center of Israel, Petah Tiqwa, Not set
Sheba Medical Center, Tel Aviv, Not set
Ospedale G. Salesi, Ancona, Not set
Universitŕ degli studi di Bari, Bari, Not set
Ospedali Riuniti, Bergamo, Not set
Ospedale S. Orsola, Bologna, Not set
Ospedale Regionale per le Microcitemie, Cagliari, Not set
Azienda Ospedaliera di Cosenza, Cosenza, Not set
Azienda Ospedaliera A. Meyer, Firenze, Not set
Istituto Giannina Gaslini, Genua, Not set
Istituto Nazionale Tumori di Milano, Milano, Not set
Azienda Ospedal. Univ. di Modena, Modena, Not set
Sec. Univ. degli Studi di Napoli - Policlinico, Napoli, Not set
Clinica di Oncoematologia Pediatrica Padova, Padova, Not set
Ospedale dei Bambini, Palermo, Palermo, Not set
Azienda Ospedaliera Universitaria di Parma-Oncoematologia Pediatrica, Parma, Not set
Policlinico San Matteo, Pavia, Not set
Ospedale Civile Spirito Santo, Pescara, Not set
Ospedale "Infermi ", Rimini, Not set
Policlinico Borgo Roma, Roma, Not set
Ospedale Bambino Gesu, Rome, Not set
Casa Sollievo della Sofferenza, San Giovanni Rotondo, Not set
O.I.R.M. - S. Anna, Torino, Not set
Istituto per l'Infanzia "Burlo Garofolo", Trieste, Not set
Haukeland University Hospital, Bergen, Not set
Rikshospitalet, Oslo, Not set
University Hospital of North-Norway, Tromso, Not set
Medical University of Bialystok, Bialystok, Not set
Medical University of Bydgoszcz, Bydgoszcz, Not set
Childrens' Hospital in Chorzów, Chorzów, Not set
Medical University in Gdansk, Gdansk, Not set
Upper Silesian Centre of Child and Mother's Care, Katowice, Not set
University Children's Hospital, Kraków, Not set
Children's University Hospital in Lublin, Lublin, Not set
University of Medical Sciences Poznan, Poznan, Not set
Institute Mother and Child, Warschau, Not set
Wroclaw Medical University, Wroclaw, Not set
Ipofg-Crl, Lissabon, Not set
University Hospital F. D. Roosevelt, Banská Bystrica, Not set
University Children's Hospital Ljubljana, Ljubljana, Not set
H. General de Alicante, Alicante, Not set
Hospital Vall d'Hebron, Barcelona, Not set
Hospital de Cruces, Bilbao, Not set
Complejo Hospitalario de Jaen, Jaen, Not set
H . Materno-Infantil Teresa Herrera, La Coruna, Not set
H. Monteprincipe, Madrid, Not set
Hospital 12 de Octubre, Madrid, Not set
H Central de Asturias, Oviedo, Not set
H. C. U. de Salamanca, Salamanca, Not set
H. de Donostia Ntra. Sra. de Aranzazu, San Sebastián, Not set
H. General de Galicia, Santiago De Compostela, Not set
Hospital Virgen del Rocio, Sevilla, Not set
Carlos Haya, Valencia, Not set
Hospital Infantil La Fe, Valencia, Not set
H Clinico-Universitario, Zaragoza, Not set
Queen Silvia's Children's Hospital, Göteburg, Not set
Childrens Hospital Linkoping, Linkoping, Not set
University Children's Hospital, Geneva, Not set
CHUV, Lausanne, Not set
Aberdeen: Royal Aberdeen Children's Hospital, Aberdeen, Not set
Royal Belfast Hospital for Sick Children, Belfast, Not set
Birmingham Children's Hospital, Birmingham, Not set
Bristol Royal Hospital for Children, Bristol, Not set
Addenbrooke's NHS Trust, Cambridge, Not set
Llandough Hospital, Cardiff, Not set
Edinburgh Royal Hospital for Sick Children, Edinburgh, Not set
Glasgow Royal Hospital for Sick Children, Glasgow, Not set
Leeds: St James's University Hospital, Leeds, Not set
Leicester Royal Infirmary, Leicester, Not set
Liverpool: Alder Hey Children's Hospital, Liverpool, Not set
Great Ormond Street Hospital, London, Not set
St Bartholomew's Hospital, London, Not set
UCLH University College London Hospital, London, Not set
Royal Manchester Children's Hospital, Manchester, Not set
Newcastle: Royal Victoria Infirmary, Newcastle, Not set
Nottingham: Queen's Medical Centre, Nottingham, Not set
Oxford: John Radcliffe Hospital, Oxford, Not set
Sheffield Children's Hospital, Sheffield, Not set
Southampton General Hospital, Southhampton, Not set
Royal Marsden Hospital, Sutton, Not set
Conditions: Neuroblastoma
Phase Ib/II Study of M3814 With Etoposide and Cisplatin in Small Cell Lung Cancer (SCLC) Extensive Disease (ED)
Terminated
M3814 is an investigational drug under evaluation for treatment of lung cancer. The purpose of the study was to assess the Safety and Efficacy of M3814 in combination with chemotherapy with SCLC ED.
M3814 is an investigational drug under evaluation for treatment of lung cancer. The purpose of the study was to assess the Safety and Efficacy of M3814 in combination with chemotherapy with SCLC ED. Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
09/11/2020
Locations: Research site, Mesa, Arizona +79 locations
Research site, Mesa, Arizona
Research site 1, Santa Rosa, California
Research site, Santa Rosa, California
Research site, Whittier, California
Research site, Danbury, Connecticut
Research site, Norwalk, Connecticut
Research site, Columbus, Georgia
Research site, Newnan, Georgia
Research site, Topeka, Kansas
Research site, Ashland, Kentucky
Research site, Billings, Montana
Research site, Pinehurst, North Carolina
Research site, Cincinnati, Ohio
Research site, Portland, Oregon
Research site, Philadelphia, Pennsylvania
Research site, Houston, Texas
Research site, Aalst, Not set
Research site, Charleroi, Not set
Research site, Edegem, Not set
Research site, Gent, Not set
Research site, Libramont, Not set
Research site, Liège, Not set
Research site, Roeselare, Not set
Research site, Yvoir, Not set
Research site 4, Sofia, Not set
Research site 2, Sofia, Not set
Research site 6, Sofia, Not set
Reasearch site 5, Sofia, Not set
Research site 3, Sofia, Not set
Research site 1, Sofia, Not set
Research site, Calgary, Alberta
Research site, St. John, New Brunswick
Research site, London, Ontario
Research site, Toronto, Ontario
Research site, Benesov, Not set
Research site, Olomouc, Not set
Research site, Aalborg, Not set
Research site, Herlev, Not set
Research site, Odense C, Not set
Research site, Freiburg, Baden Wuerttemberg
Research site, Gauting, Bavaria
Research site, Nuernberg, Bavaria
Research site, Hannover, Lower Saxony
Research site, Chemnitz, Saxony
Research site, Kiel, Schleswig-Holstein
Research site, Luebeck, Schleswig-Holstein
Research site 1, Berlin, Not set
Research site 2, Berlin, Not set
Research site 1, Budapest, Not set
Research site 2, Budapest, Not set
Research site 3, Budapest, Not set
Research site, Farkasgyepu, Not set
Research site, Szekszard, Not set
Research site, Szolnok, Not set
Research site, Rozzano, Milano
Research site, Catania, Not set
Research site, Genova, Not set
Research site, Napoli, Not set
Research site, Ravenna, Not set
Research site, Reggio Emilia, Not set
Research site, Roma, Not set
Research site, Torino, Not set
Research site, Olsztyn, Not set
Research site, Poznan, Not set
Research site, Warszawa, Not set
Research site, Wodzislaw Slaski, Not set
Research site, Baia Mare, Not set
Research site, Cluj-Napoca, Not set
Research site, Cluj-Napoca, Not set
Research site, Craiova, Not set
Research site, Timisoara, Not set
Research site, Badajoz, Not set
Research site 1, Madrid, Not set
Research site 4, Madrid, Not set
Research site 3, Madrid, Not set
Research site 2, Madrid, Not set
Research site, Hull, East Riding Of Yorkshire
Research site, London, Greater London
Research site, Sheffield, South Yorkshire
Research site, Glasgow, Strathclyde
Conditions: Small Cell Lung Cancer
Trial in Extensive-Disease Small Cell Lung Cancer (ED-SCLC) Subjects Comparing Ipilimumab Plus Etoposide and Platinum Therapy to Etoposide and Platinum Therapy Alone
Completed
The purpose of the study is to determine whether the addition of Ipilimumab to Etoposide and Platinum therapy will extend the lives of patients with Extensive-Stage Disease Small Cell Lung Cancer (ED-SCLC) more than Etoposide and Platinum therapy alone.
The purpose of the study is to determine whether the addition of Ipilimumab to Etoposide and Platinum therapy will extend the lives of patients with Extensive-Stage Disease Small Cell Lung Cancer (ED-SCLC) more than Etoposide and Platinum therapy alone. Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
07/06/2020
Locations: Genesis Cancer Center, Hot Springs, Arkansas +224 locations
Genesis Cancer Center, Hot Springs, Arkansas
Sutter Medical Center, Auburn, California
UCSD Moores Cancer Center, La Jolla, California
University Of Colorado Cancer Center, Aurora, Colorado
Florida Cancer Specialists S., Fort Myers, Florida
Cancer Specialists, LLC, Jacksonville, Florida
Lake City Cancer Care, Lake City, Florida
Florida Cancer Specialists, Saint Petersburg, Florida
Medical Oncology, LLC, Augusta, Georgia
Quincy Medical Group, Quincy, Illinois
Presence Medical Group Hematology Oncology, Skokie, Illinois
SIU School Of Medicine, Springfield, Illinois
St. Francis Medical Group Oncology And Hematology Specialist, Indianapolis, Indiana
Cancer Center Of Kansas, Wichita, Kansas
Ashland Bellefonte Cancer Center, Ashland, Kentucky
University Of Kentucky, Lexington, Kentucky
Montgomery Cancer Center, Mount Sterling, Kentucky
St Joseph Mercy Hospital, Ypsilanti, Michigan
St. Luke'S Cancer Institute, Kansas City, Missouri
Southeast Nebraska Hematology & Oncology Consultants, P.C., Lincoln, Nebraska
Regional Cancer Care Associates, LLC/Cherry Hill Division, Cherry Hill, New Jersey
Memorial Sloan Kettering Nassau, New York, New York
Gabrail Cancer Center, Canton, Ohio
Oncology Hematology Care, Incorporated, Cincinnati, Ohio
University Hospitals, Cleveland, Ohio
Signal Point Clinical Research Center, Llc, Middletown, Ohio
Oklahoma Cancer Specialists and Research Institute, LLC, Tulsa, Oklahoma
Providence Portland Medical Center, Portland, Oregon
Kaiser Permanente, Portland, Oregon
Chattanooga Oncology Hematology Associates, Chattanooga, Tennessee
Associated in Oncology and Hematology, Chattanooga, Tennessee
The Jones Clinic, PC, Germantown, Tennessee
Tennessee Cancer Specialists, Knoxville, Tennessee
Thompson Cancer Survival Center, Knoxville, Tennessee
Tennessee Oncology, PLLC, Nashville, Tennessee
Henry-Joyce Cancer Center, Nashville, Tennessee
University Of Texas, M. D. Anderson Cancer Center, Houston, Texas
Joe Arrington Cancer Research And Treatment Center, Lubbock, Texas
Huntsman Cancer Hospital, Salt Lake City, Utah
Virginia Cancer Institute, Richmond, Virginia
Virginia Commonwealth University, Richmond, Virginia
Mary Babb Randolph Cancer Center, Morgantown, West Virginia
Local Institution, Berazategui, Buenos Aires
Local Institution, Buenos Aires, Not set
Local Institution, Ciudad Autonoma de Buenos Aires, Not set
Local Institution, Provincia De Sante Fe, Not set
Local Institution, Kogarah, New South Wales
Local Institution, Wollongong, New South Wales
Local Institution, Chermside, Queensland
Local Institution, Bedford Park, South Australia
Local Institution, Fitzroy, Victoria
Local Institution, Wodonga, Victoria
Local Institution, Perth, Western Australia
Local Institution, Linz, Not set
Local Institution, Salzburg, Not set
Local Institution, Wien, Not set
Local Institution, Wien, Not set
Local Institution, Brussels, Not set
Local Institution, Edegem, Not set
Local Institution, Leuven, Not set
Local Institution, Sint Niklaas, Not set
Local Institution, Yvoir, Not set
Local Institution, Passo Fundo, RS, Not set
Local Institution, Sao Paulo/SP, Not set
Local Institution, SP, Not set
Local Institution, Montreal, Quebec
Local Institution, Montreal, Quebec
Local Institution, Vina Del Mar, Valparaiso
Local Institution, Santiago, Not set
Local Institution, Santiago, Not set
Local Institution, Guangzhou, Guangdong
Local Institution, Guangzhou, Guangdong
Local Institution, Harbin, Heilongjiang
Local Institution, Wuhan, Hubei
Local Institution, Nangjing, Jiangsu
Local Institution, Soochow, Jiangsu
Local Institution, Changchun, Jilin
Local Institution, Xi'an, Shaanxi
Local Institution, Xi'an, Shaanxi
Local Institution, Chengdu City, Sichuan
Local Institution, Urumqi, Xinjiang
Local Institution, Hangzhou City, Zhejiang
Local Institution, Hangzhou City, Zhejiang
Local Institution, Beijing, Not set
Local Institution, Beijing, Not set
Local Institution, Beijing, Not set
Local Institution, Beijing, Not set
Local Institution, Shanghai, Not set
Local Institution, Shanghai, Not set
Local Institution, Cordoba, Not set
Local Institution, Ostrava - Poruba, Not set
Local Institution, Praha 8, Not set
Local Institution, Caen, Not set
Local Institution, Rennes Cedex 9, Not set
Local Institution, Toulouse Cedex 9, Not set
Local Institution, Vandoeuvre-les-nancy, Not set
Local Institution, Bad Berka, Not set
Local Institution, Bochum, Not set
Local Institution, Dresden, Not set
Local Institution, Erlangen, Not set
Local Institution, Frankfurt am Main, Not set
Local Institution, Gauting, Not set
Local Institution, Grosshansdorf, Not set
Local Institution, Hamburg, Not set
Local Institution, Heidelberg, Not set
Local Institution, Kassel, Not set
Local Institution, Mainz, Not set
Local Institution, Mannheim, Not set
Local Institution, Munchen, Not set
Local Institution, Oldenburg, Not set
Local Institution, Ulm, Not set
Local Institution, Hong Kong, Not set
Local Institution, Kowloon, Not set
Local Institution, Budapest, Not set
Local Institution, Budapest, Not set
Local Institution, Budapest, Not set
Local Institution, Farkasgyepu, Not set
Local Institution, Matrahaza, Not set
Local Institution, Pecs, Not set
Local Institution, Sopron, Not set
Local Institution, Szolnok, Not set
Local Institution, Dublin, Not set
Local Institution, Dublin, Not set
Local Institution, Limerick, Not set
Local Institution, Beer Sheva, Not set
Local Institution, Kfar-saba, Not set
Local Institution, Petah-tikva, Not set
Local Institution, Ramat-gan, Not set
Local Institution, Zerifin, Not set
Local Institution, Livorno, Not set
Local Institution, Lucca, Not set
Local Institution, Meldola (FC), Not set
Local Institution, Siena, Not set
Local Institution, Nagoya-shi, Aichi
Local Institution, Nagoya, Aichi
Local Institution, Kashiwa, Chiba
Local Institution, Matsuyama-shi, Ehime
Local Institution, Sapporo, Hokkaido
Local Institution, Kanazawa-shi, Ishikawa
Local Institution, Yokohama-Shi, Kanagawa
Local Institution, Yokohama-shi, Kanagawa
Local Institution, Natori, Miyagi
Local Institution, Kurashiki-shi, Okayama
Local Institution, Kurashiki-shi, Okayama
Local Institution, Hirakata-shi, Osaka
Local Institution, Takatsuki, Osaka
Local Institution, Sunto-gun, Shizuoka
Local Institution, Chuo-ku, Tokyo
Local Institution, Ube-shi, Yamaguchi
Local Institution, Akashi, Hyogo, Not set
Local Institution, Fukoka, Not set
Local Institution, Fukuoka, Not set
Local Institution, Osaka, Not set
Local Institution, Oskaka, Not set
Local Institution, Sapporo, Hokkaido, Not set
Local Institution, Sendai, Miyagi, Not set
Local Institution, Tokyo, Not set
Local Institution, Goyang-si, Gyeonggji-do
Local Institution, Hwasun-eup, Hwasun-gun, Jeonnam
Local Institution, Busan, Not set
Local Institution, Seoul, Not set
Local Institution, Seoul, Not set
Local Institution, Seoul, Not set
Local Institution, Seoul, Not set
Local Institution, Suwon, Not set
Local Institution, Suwon, Not set
Local Institution, Guadalajara, Jalisco
Local Institution, San Luis Potosi, S.l.p., Not set
Local Institution, 's-Hertogenbosch, Not set
Local Institution, Breda, Not set
Local Institution, Eindhoven, Not set
Local Institution, Cercado, Not set
Local Institution, Lima, Not set
Local Institution, Lima, Not set
Local Institution, Elblag, Not set
Local Institution, Karkow, Not set
Local Institution, Lublin, Not set
Local Institution, Otwock, Not set
Local Institution, Poznan, Not set
Local Institution, Torun, Not set
Local Institution, Warszawa, Not set
Local Institution, Coimbra, Not set
Local Institution, Lisboa, Not set
Local Institution, Cluj Napoca, Judetul CLUJ
Local Institution, Craiova, Judetul DOLJ
Local Institution, Bucuresti, Not set
Local Institution, Cluj, Not set
Local Institution, Chelyabinsk, Not set
Local Institution, Krasnodar, Not set
Local Institution, Kursk, Not set
Local Institution, Moscow, Not set
Local Institution, Pyatigorsk, Not set
Local Institution, Saint Petersburg, Not set
Local Institution, Saint Petersburg, Not set
Local Institution, St. Petersburg, Not set
Local Institution, St. Petersburg, Not set
Local Institution, Port Elizabeth, Eastern CAPE
Local Institution, Cape Town, Western CAPE
Local Institution, Pretoria, Not set
Local Institution, A Coruna, Galicia
Local Institution, Barcelona, Not set
Local Institution, Benidorm-alicante, Not set
Local Institution, Castellon, Not set
Local Institution, Lleida, Not set
Local Institution, Majadahonda, Not set
Local Institution, Malaga, Not set
Local Institution, Valencia, Not set
Local Institution, Linkoping, Not set
Local Institution, Stockholm, Not set
Local Institution, Uppsala, Not set
Local Institution, Basel, Not set
Local Institution, Winterthur, Not set
Local Institution, Zuerich, Not set
Local Institution, Changhua City, Not set
Local Institution, Taichung, Not set
Local Institution, Taipei, Not set
Local Institution, Taoyuan County, Not set
Local Institution, Chiang Mai, Not set
Local Institution, Songkhla, Not set
Local Institution, Withington, Manchester
Local Institution, London, Not set
Local Institution, London, Not set
Local Institution, Preston, Not set
Local Institution, Sutton, Not set
Local Institution, Truro, Not set
Conditions: Small Cell Lung Carcinoma
A Phase III Randomised Trial of Peri-Operative Chemotherapy Versus sUrveillance in Upper Tract Urothelial Cancer (POUT)
Unknown
POUT is a multi-centred randomised controlled phase III trial. 345 patients who have undergone nephro-ureterectomy, are surgically staged pT2-pT4, N0-3 or are pT1 and node positive, and who are fit for adjuvant chemotherapy, will be randomised to four cycles of adjuvant platinum based chemotherapy (experimental group) or surveillance (control group). Participants will be followed up according to routine practice.
Primary endpoint: Disease-free survival (DFS)
Secondary endpoints:
* Overall Sur... Read More
POUT is a multi-centred randomised controlled phase III trial. 345 patients who have undergone nephro-ureterectomy, are surgically staged pT2-pT4, N0-3 or are pT1 and node positive, and who are fit for adjuvant chemotherapy, will be randomised to four cycles of adjuvant platinum based chemotherapy (experimental group) or surveillance (control group). Participants will be followed up according to routine practice.
Primary endpoint: Disease-free survival (DFS)
Secondary endpoints:
* Overall Survival
* Metastasis free survival
* Incidence of bladder second primary tumours
* Incidence of contralateral primary tumours
* Acute and late toxicity
* Treatment compliance
* Quality of life Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
04/30/2020
Locations: William Harvey Hospital, Ashford-Kent, England +60 locations
William Harvey Hospital, Ashford-Kent, England
North Devon District Hospital, Barnstaple, England
Basildon University Hospital, Basildon, England
Kent and Canterbury Hospital, Canterbury, England
Royal Free Hospital, Hampstead, London, England
Ipswich Hospital NHS Trust, Ipswich, England
St. James's University Hospital, Leeds, England
Barts and the London School of Medicine, London, England
Maidstone Hospital, Maidstone, England
Christie Hospital NHS Trust, Manchester, England
Queen Elizabeth The Queen Mother Hospital, Margate, England
Clatterbridge Centre for Oncology NHS Trust, Merseyside, England
Nottingham City Hospital NHS Trust, Nottingham, England
Peterborough Hospitals Trust, Peterborough, England
Rosemere Cancer Centre at Royal Preston Hospital, Preston, England
Cancer Research Centre at Weston Park Hospital, Sheffield, England
Royal Marsden Hosital, Sutton, Surrey, England
Southend University Hospital NHS Foundation Trust, Westcliff-On-Sea, England
New Cross Hospital, Wolverhampton, England
Ayr Hospital, Ayr, Scotland
Velindre Cancer Center at Velinde Hospital, Cardiff, Wales
Singleton Hospital, Swansea, Wales
Bristol Haematology and Oncology Centre, Bristol, Not set
Southmead Hospital, Bristol, Not set
Royal Marsden Hospital, Chelsea, Not set
University Hospitals Coventry and Warwickshire NHS Trust, Coventry, Not set
Darent Valley Hospital, Dartford, Not set
Royal Derby Hospital, Derby, Not set
Royal Bournemouth General Hospital, Dorset, Not set
Western General Hospital, Edinburgh, Not set
Royal Devon and Exeter Hospital, Exeter, Not set
Beatson West of Scotland Cancer Centre, Glasgow, Not set
Royal Surrey County Hospital, Guildford, Not set
Calderdale Royal Infirmary, Halifax, Not set
Huddersfield Royal Infirmary, Huddersfield, Not set
Caithness General Hospital, Inverness, Not set
Raigmore Hospital, Inverness, Not set
Leicester Royal Infirmary, Leicester, Not set
Lincoln County Hospital, Lincoln, Not set
Royal Liverpool University Hospital, Liverpool, Not set
Guy's Hospital, London, Not set
Charing Cross Hospital, London, Not set
Northwick Park Hospital, London, Not set
Manchester Royal Infirmary, Manchester, Not set
James Cook University Hospital, Middlesbrough, Not set
Freeman Hospital, Newcastle upon Tyne, Not set
Norfolk and Norwich University Hospital, Norwich, Not set
Queen Alexandra Hospital,, Portsmouth, Not set
Glan Clywd Hospital, Rhyl, Not set
Queen's Hospital,, Romford, Essex, Not set
Royal Shrewsbury Hospital, Shrewsbury, Not set
Southampton General Hospital, Southampton, Not set
Lister Hospital, Stevenage, Not set
University Hospital of North Tees, Stockton-on-Tees, Not set
Frimley Park Hospital, Surrey, Not set
The Royal Marsden Hospital, Sutton, Not set
Musgrove Park Hospital, Taunton, Not set
Torbay District General Hospital, Torbay, Not set
Royal Cornwall Hospital, Treliske, Not set
Worthing Hospital, Worthing, Not set
York District Hospital, York, Not set
Conditions: Transitional Cell Carcinoma of Ureter
M6620 First in Human Study
Completed
An Open-Label, First-in-Human Study of the Safety, Tolerability, and Pharmacokinetics (PK) of M6620 in Combination With Cytotoxic Chemotherapy in Participants With Advanced Solid Tumors
An Open-Label, First-in-Human Study of the Safety, Tolerability, and Pharmacokinetics (PK) of M6620 in Combination With Cytotoxic Chemotherapy in Participants With Advanced Solid Tumors Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
03/31/2020
Locations: Mayo Clinic Arizona, Phoenix, Arizona +30 locations
Mayo Clinic Arizona, Phoenix, Arizona
Sharp Memorial Hospital, San Diego, California
Not set, Stanford, California
Rocky Mountain Cancer Centers, LLP, Denver, Colorado
Emory University, Atlanta, Georgia
Northwestern Center for Clinical Research, Chicago, Illinois
Dana Farber Cancer Institute, Boston, Massachusetts
Breslin Cancer Center, Lansing, Michigan
University Of Minnesota Hospital, Minneapolis, Minnesota
Mayo Clinic - Rochester, Rochester, Minnesota
Washington University in St. Louis, Saint Louis, Missouri
Hackensack University Medical Center PARTNER, Hackensack, New Jersey
Long Island Jewish Medical Center - Monter Cancer Center, Lake Success, New York
University Hospitals Case Medical Center - Case Comprehensive Cancer Center at, Cleveland, Ohio
OSU - James Comprehensive Cancer Center - Division of Hematology, Columbus, Ohio
Greenville Health System, Greenville, South Carolina
Vanderbilt University Medical Center, Nashville, Tennessee
US Oncology - Texas Oncology-Midtown - Austin Midtown, Austin, Texas
Texas Oncology, P.A., Dallas, Texas
University of Texas M. D. Anderson Cancer Center - Investigational Cancer Therapeutics - Partner, Houston, Texas
Texas Oncology San Antonio Medical Cente, San Antonio, Texas
Virginia Cancer Specialists, PC, Fairfax, Virginia
Virginia Oncology Associates - Hampton, Norfolk, Virginia
Northwest Cancer Specialists , P.C., Vancouver, Washington
Freeman Hospital - PARENT, Newcastle Upon Tyne, England
Churchill Hospital - PARENT, Oxford, England
Beatson West of Scotland Cancer Centre - Dept of Medical Oncology, Glasgow, Scotland
Royal Marsden Hospital - Dept of Oncology, Sutton, Surrey
Guy's Hospital - PARENT, London, Not set
Sarah Cannon Research Institute UK, London, Not set
The Christie - Dept of Oncology, Manchester, Not set
Conditions: Advanced Solid Tumor
Study of the Safety and Efficacy of Amatuximab in Combination With Pemetrexed and Cisplatin in Subjects With Unresectable Malignant Pleural Mesothelioma (MPM)
Terminated
This study was originally designed as a multicenter, double-blind, randomized, parallel-group study, using a placebo control or amatuximab 5 milligrams per kilogram (mg/kg), administered weekly, designed to evaluate the safety and efficacy of amatuximab in combination with pemetrexed and cisplatin in participants with unresectable Malignant Pleural Mesothelioma (MPM) who have not received prior systemic therapy.
Per a business decision made by the Sponsor, participants who were randomized to am... Read More
This study was originally designed as a multicenter, double-blind, randomized, parallel-group study, using a placebo control or amatuximab 5 milligrams per kilogram (mg/kg), administered weekly, designed to evaluate the safety and efficacy of amatuximab in combination with pemetrexed and cisplatin in participants with unresectable Malignant Pleural Mesothelioma (MPM) who have not received prior systemic therapy.
Per a business decision made by the Sponsor, participants who were randomized to amatuximab and were still on active treatment at the time of the protocol amendment may have consented to continue to receive weekly treatment with amatuximab until disease progression or intolerable toxicity at the discretion of the principal investigator. Participants randomized to placebo or who were in follow-up at the time of the amendment have been discontinued from the study. Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
03/04/2020
Locations: Not set, La Jolla, California +48 locations
Not set, La Jolla, California
Not set, Newark, Delaware
Not set, Bethesda, Maryland
Not set, Rochester, Minnesota
Not set, Philadelphia, Pennsylvania
Not set, Dallas, Texas
Not set, Spokane, Washington
Not set, Camperdown, New South Wales
Not set, Auchenflower, Queensland
Not set, Richmond, Victoria
Not set, Perth, Western Australia
Not set, Caen, Not set
Not set, Creteil, Not set
Not set, La Tronche, Not set
Not set, Lille, Not set
Not set, Lyon Cedex, Not set
Not set, Marseille, Not set
Not set, Rennes, Not set
Not set, Toulouse, Not set
Not set, Berlin, Not set
Not set, Esslingen, Not set
Not set, Frankfurt am Main, Not set
Not set, Gauting, Not set
Not set, Hamburg, Not set
Not set, Hanover, Not set
Not set, Löwenstein, Not set
Not set, Ulm, Not set
Not set, Wöhrendamm, Not set
Not set, Rozzano, Milano
Not set, Pisa, Paradisa 2
Not set, Alessandria, Not set
Not set, Aviano, Not set
Not set, Bari, Not set
Not set, Bergamo, Not set
Not set, Genoa, Not set
Not set, Genova, Not set
Not set, Monza, Not set
Not set, Orbassano, Not set
Not set, Parma, Not set
Not set, Maidstone, Kent
Not set, Dundee, Not set
Not set, Hereford, Not set
Not set, Leicester, Not set
Not set, London, Not set
Not set, Middlesex, Not set
Not set, Preston, Not set
Not set, Southampton, Not set
Not set, Swindon, Not set
Not set, Taunton, Not set
Conditions: Mesothelioma, Malignant
Study of Amrubicin With or Without Cisplatin Versus Etoposide-cisplatin for Extensive Stage Small Cell Lung Cancer
Completed
The purpose of the study is to document the activity and safety of single agent amrubicin, amrubicin combined with cisplatin, and etoposide combined with cisplatin as first-line treatment in extensive disease small cell lung cancer.
The purpose of the study is to document the activity and safety of single agent amrubicin, amrubicin combined with cisplatin, and etoposide combined with cisplatin as first-line treatment in extensive disease small cell lung cancer. Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
11/14/2019
Locations: Algemeen Ziekenhuis Middelheim, Antwerpen, Not set +24 locations
Algemeen Ziekenhuis Middelheim, Antwerpen, Not set
Universitair Ziekenhuis Antwerpen, Edegem, Not set
Universiteit Gent, Gent, Not set
U.Z. Gasthuisberg, Leuven, Not set
Domaine Universitaire du Sart-Tilman, Liege, Not set
Centre Hospitalier Regional de la Citadelle, Liege, Not set
Clinique Sainte Elisabeth, Namur, Not set
Instituto Nazionale per la Ricerca sul Cancro, Genova, Not set
Universita Degli Studi Di Udine, Udine, Not set
Academisch Medisch Centrum, Amsterdam, Not set
The Netherlands Cancer Institute Antoni Van Leeuwenhoekziekenhuis, Amsterdam, Not set
Medisch Spectrum Twente - Dept of Pulmonary Diseases, Enschede, Not set
Leiden University Medical Centre, Leiden, Not set
Academisch Ziekenhuis Maastricht, Maastricht, Not set
Isala Kliniek, Zwolle, Not set
Medical University of Gdansk - Dept Radiotherapy, Gdansk, Not set
Clatterbridge Centre for Oncology NHS Trust, Bebington, Merseyside
University of Dundee - Ninewells Hospital, Dundee, Scotland
Belfast City Hospital, Belfast, Not set
Western General Hospital, Edinburgh, Not set
Princess Royal Hospital, Hull, Not set
Royal Marsden Hospital, London, London, Not set
Christie Hospital, Manchester, Not set
Sir Bobby Robson Cancer Trials Research Centre, Newcastle-Upon-Tyne, Not set
Royal Marsden Hospital Lung Unit, Sutton, Not set
Conditions: Small Cell Lung Cancer
A Phase I/II Safety and Efficacy Study of PCI of Gemcitabine and Chemotherapy in Patients With Cholangiocarcinomas
Completed
This is a Phase I Dose Escalation Study in which the safety, tolerability and efficacy of Amphinex®--induced Photochemical Internalisation (PCI) of Gemcitabine followed by Gemcitabine/Cisplatin Chemotherapy will be assessed in patients with advanced inoperable cholangiocarcinomas.
This is a Phase I Dose Escalation Study in which the safety, tolerability and efficacy of Amphinex®--induced Photochemical Internalisation (PCI) of Gemcitabine followed by Gemcitabine/Cisplatin Chemotherapy will be assessed in patients with advanced inoperable cholangiocarcinomas. Read Less
Gender:
ALL
Ages:
18 years and above
Trial Updated:
10/28/2019
Locations: CHU Angers, Angers, Maine-et-Loire +10 locations
CHU Angers, Angers, Maine-et-Loire
Klinikum rechts der Isar, Technische Universität München, Munich, Bayern
Klinikum der Ludwig-Maximilians-Universität, München, Bayern
Klinikum der Johann Wolfgang Goethe-Universität, Frankfurt am Main, Hessen
Universitätsklinikum Essen, Essen, Nordrhein-Westfalen
Klinikum Ludwigshafen, Ludwigshafen, Rheinland-Pfalz
Universitätsklinikum Leipzig, Leipzig, Sachsen
Charité, Campus Mitte, Berlin, Not set
Universitätsklinikum Carl Gustav Carus an der Technischen Universität Dresden, Dresden, Not set
Oslo Universtiy Hospital, Oslo, Not set
University Hospital Aintree, Aintree, Liverpool
Conditions: Cholangiocarcinoma
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