A Study to Learn About the Investigational Medicine Called PF-06821497 (Mevrometostat) in Men With mCRPC Who Were Previously Treated With Abiraterone Acetate for Prostate Cancer (MEVPRO-1).
Recruiting
Pfizer MEVPRO-1 (C2321014) is a randomized, open-label, multi-center clinical trial evaluating whether combining the study medicine (PF-06821497) with enzalutamide is safe and effective compared to physician's choice of either second-line androgen receptor (AR) directed therapy with enzalutamide or docetaxel (chemotherapy) for treating metastatic castration-resistant prostate cancer (mCRPC) after progression on prior abiraterone acetate treatment. The primary objective of this clinical trial is... Read More
Gender:
MALE
Ages:
18 years and above
Trial Updated:
08/05/2025
Locations: Urology Centers of Alabama, Homewood, Alabama +220 locations
Conditions: Metastatic Castrate Resistant Prostate Cancer (mCRPC)
DAREONᵀᴹ-8: A Study to Test How Well Different Doses of BI 764532 in Addition to Standard of Care Are Tolerated by People With Advanced Small Cell Lung Cancer
Recruiting
This study is open to adults with extensive stage small cell lung cancer. The study is in people with advanced cancer that are eligible for standard of care including chemotherapy and anti-PD-L1 (Programmed Cell Death Ligand 1) immunotherapy. The purpose of this study is to find out the highest dose of BI 764532 that people can tolerate when taken together with standard of care. BI 764532 is an antibody-like molecule that may help the immune system fight cancer. Participants get BI 764532 and d... Read More
Gender:
ALL
Ages:
18 years and above
Trial Updated:
08/05/2025
Locations: Orlando Health Cancer Institute, Orlando, Florida +21 locations
Conditions: Small Cell Lung Carcinoma (SCLC)
Pain Control and Quality of Recovery After Intravenous Methadone Versus Intrathecal Morphine in Major Abdominal Surgery
Recruiting
Moderate to severe postoperative pain is relatively common after major abdominal surgery. It is associated with less than optimal surgical experience, poor quality of recovery, and the development of persistent postsurgical pain. Opioids remain a significant component of postoperative pain management. Side effects of opioids used for the treatment of postoperative pain include constipation, pruritus, nausea, and vomiting. Enhanced recovery after surgery (ERAS) protocols involve the utilization o... Read More
Gender:
ALL
Ages:
Between 18 years and 75 years
Trial Updated:
08/05/2025
Locations: University of Virginia, Charlottesville, Virginia
Conditions: Pain, Postoperative
A Study to Find Out How Nusinersen is Processed in the Body When Given Through the ThecaFlex DRx™ System in Adult and Pediatric Participants With Spinal Muscular Atrophy (PIERRE-PK)
Recruiting
In this PIERRE-PK study, researchers will learn how the body processes nusinersen when it is given through the ThecaFlex DRx™ System, compared to when nusinersen is given by lumbar puncture (LP). The ThecaFlex DRx system is an investigational implantable medical device developed by Alcyone Therapeutics, Inc. It consists of a catheter, which is a flexible tube, connected to a port which is placed under the skin. Alcyone Therapeutics, Inc. has an ongoing study called PIERRE to test the ThecaFlex D... Read More
Gender:
ALL
Ages:
3 years and above
Trial Updated:
08/05/2025
Locations: Children's Hospital of Orange County, Orange, California +14 locations
Conditions: Muscular Atrophy, Spinal
A Study of Investigational Agents in Participants With Previously Treated Stage IV Nonsquamous Non-small Cell Lung Cancer (NSCLC) (MK-3475-01H/KEYMAKER-U01)
Recruiting
Researchers are looking for new ways to treat metastatic nonsquamous non-small cell lung cancer (NSCLC) that has been treated before. Metastatic means the cancer has spread to other parts of the body. Nonsquamous means the cancer did not start in squamous cells, which are flat cells that line the inside of the lungs. Standard treatment (usual treatment) for NSCLC is surgery, then immunotherapy with or without chemotherapy after surgery. Immunotherapy is a treatment that helps the immune system... Read More
Gender:
ALL
Ages:
18 years and above
Trial Updated:
08/05/2025
Locations: MedStar Franklin Square Medical Center ( Site 0033), Baltimore, Maryland +8 locations
Conditions: Carcinoma, Non-Small-Cell Lung
A Trial to Investigate Benralizumab in Children With Eosinophilic Diseases
Recruiting
The main purpose of study is to assess the safety, tolerability, and pharmacokinetic (PK) of benralizumab.
Gender:
ALL
Ages:
Between 6 years and 17 years
Trial Updated:
08/05/2025
Locations: Research Site, Aurora, Colorado +5 locations
Conditions: Eosinophilic Granulomatosis With Polyangiitis (EGPA)
A Phase 0 Multicenter Study of the Pharmacodynamic Effects of Intratumoral Microdose Administration of PBA-0111 in Patients With Solid Tumors
Recruiting
This is a multi-center, single arm, open-label, localized pharmacodynamic biomarker Phase 0 trial designed to study the biological effects within the tumor microenvironment of PBA-0111 when administered intratumorally in microdose quantities via the CIVO device.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
08/05/2025
Locations: LSU Health Sciences Center, Shreveport, Louisiana
Conditions: Head and Neck Squamous Cell Carcinoma, Soft Tissue Sarcoma Adult, Triple Negative Breast Cancer
Nephroureterectomy With and Without Lymph Node Dissection for Upper Tract Urothelial Cell Carcinoma
Recruiting
The goal of this study is to conduct the first randomized-controlled trial to determine the oncologic efficacy of lymph node dissection in participants with upper tract urothelial cell carcinoma. The main questions it aims to answer are: * To determine oncologic outcomes, specifically 2-year recurrence-free survival * To determine other oncologic outcomes including treatment-free, cancer-specific and overall survival * To determine time to recurrence and recurrence patterns * To determine use o... Read More
Gender:
ALL
Ages:
19 years and above
Trial Updated:
08/05/2025
Locations: University of Florida Health Science Center, Gainesville, Florida +2 locations
Conditions: Urothelial Carcinoma
Sinus Disease in Young Children With Cystic Fibrosis
Recruiting
This is a prospective, observational study examining the impact of highly effective cystic fibrosis transmembrane conductance regulator (CFTR) modulators on chronic rhinosinusitis (CRS) and olfactory dysfunction (OD) in young children with cystic fibrosis (YCwCF). This study involves two groups: children 2-8 years old, inclusive at initial visit, receiving highly effective modulator therapy (HEMT), and a control group of children 2-8 years old, inclusive at initial visit, not receiving HEMT. Out... Read More
Gender:
ALL
Ages:
Between 2 years and 8 years
Trial Updated:
08/05/2025
Locations: Children's Hospital Colorado, Aurora, Colorado +5 locations
Conditions: Cystic Fibrosis in Children, Cystic Fibrosis, Chronic Rhinosinusitis (Diagnosis), Olfactory Disorder, Olfactory Impairment
A Natural History Study Seeks to Understand the Clinical, Genomic, Pharmacological, Laboratory, and Dietary Determinates of Pyrimidine and Purine Metabolism Disorders
Recruiting
Background: Pyrimidine and purine metabolism disorders (DPPMs) affect how the body metabolizes chemicals called pyrimidines and purines. DPPMs can cause dysfunctions throughout the body, especially in the brain, blood, kidneys, and immune system. People with DPPMs might have no symptoms, mild symptoms, or they may have severe, chronic symptoms, that can be fatal. DPPMs are not well understood, and researchers want to learn more about what causes them and how to treat them. Objective: To learn... Read More
Gender:
ALL
Ages:
Between 1 month and 100 years
Trial Updated:
08/05/2025
Locations: National Institutes of Health Clinical Center, Bethesda, Maryland
Conditions: Purine-Pyrimidine Metabolism, Metabolic Disease, AICDA, OMIM *605257, Immunodeficiency With Hyper-IgM, Type 2; HIGM2, UNG, OMIM *191525, Hyper-IgM Syndrome 5, NT5C3A, OMIM *606224, Anemia, Hemolytic, Due to UMPH1 Deficiency, UMPS, OMIM *613891, Orotic Aciduria, DHODH, OMIM *126064, Miller Syndrome (Postaxial Acrofacial Dysostosis), DPYD, OMIM *274270, Dihydropyrimidine Dehydrogenase Deficiency, DPYS, OMIM *613326, Dihydropyrimidinase Deficiency, UPB1, OMIM *606673, Beta-ureidopropionase Deficiency, CAD, *1140120, Developmental and Epileptic Encephalopathy, ADA2, OMIM *607575,Sneddon Syndrome; VAIHS, PNP, OMIM *164050, Nucleoside Phosphorylase Deficiency, ADSL, OMIM *608222, Adenylosuccinate Lyase Deficiency, ITPA, OMIM *147520, Inosine Triphosphatase Deficiency; Developmental and Epileptic Encephalopathy 35, AMPD2, OMIM *102771, Spastic Paraplegia 63; Pontocerebellar Hypoplasia, PRPS1 SA, OMIM *311850 Gout, PRPS-related Phosphoribosylpyrophosphate Synthetase Superactivity, PRPS1 Def, OMIM *311850, Arts Syndrome; Charcot-Marie-Tooth Disease, SLC22A12, OMIM *607096 Hypouricemia, SLC2A9, OMIM *606142 Hypouricemia, XDH, OMIM *607633, Xanthinuria Type 1, HPRT1, OMIM *308000 Lesch-Nyhan Disease, APRT, OMIM *102600, Adenine Phosphoribosyltransferase Deficiency, IMPDH1, OMIM *146690, Retinitis Pigmentosa Type 10, Leber Congenital Amauriosis Type 11, TPMT, OMIM *187680, Thoipurines, Poor Metabolism of, AMPD1, OMIM *102770, Myopathy Due to Myoadenylate Deaminase Deficiency, AK1, OMIM *103000, Adenylate Kinase Deficiency, AMPD3, OMIM*102772, AMP Deaminase Deficiency
eTMS for Veterans and First Responders With PTSD
Recruiting
A battery of physiological and behavioral data will be collected before and after application of eTMS. Participants will be veterans or first responders diagnosed with PTSD. Study will be a double-blind, sham-controlled, parallel group, randomized clinical trial.
Gender:
ALL
Ages:
Between 18 years and 65 years
Trial Updated:
08/05/2025
Locations: Fralin Biomedical Research Institute, Roanoke, Virginia
Conditions: Post Traumatic Stress Disorder
Axatilimab for Sclerotic Chronic Graft-versus-Host Disease
Recruiting
This phase II trial tests how well axatilimab works in treating patients with thickening or hardening (sclerosis) of the skin related to chronic graft-versus-host disease after a donor stem cell transplant. Chronic graft-versus-host disease (cGVHD) remains a major complication of donor stem cell transplants. Sclerosis, while not associated with a higher risk of death, can lead to serious disabilities. Usual treatments for cGVHD can be associated with significant side effects and unsatisfactory o... Read More
Gender:
ALL
Ages:
18 years and above
Trial Updated:
08/05/2025
Locations: Moffitt Cancer Center, Tampa, Florida +2 locations
Conditions: Chronic Graft Versus Host Disease