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Directory of Clinical Studies

HIV (Adult)AI266-959Study to Determine the Effect of Efavirenz on the ECG QTcF Interval in Healthy SubjectsRecruiting
HIV (Adult)AI424-517Taste Properties of Atazanavir and CobicistatRecruiting
HIV (Adult)AI438-047Attachment Inhibitor Comparison in Heavily Treatment Experienced PatientsRecruiting
Hepatitis CAI444-257A Multicenter Treatment Protocol of Daclatasvir (BMS-790052) in Combination With Sofosbuvir for the Treatment of Post-Liver Transplant Subjects With Chronic Hepatitis CAvailable
HIV (Adult)AI468-048Strategy-confirming Study of BMS-955176 to Treat HIV-1 Infected Treatment-experienced AdultsNot yet recruiting
Lung Cancer, CancerCA001-030Multiple Ascending Dose w/Expansion in Relapsed/Refractory SCLCRecruiting
CancerCA002-001Phase I Ascending Multiple-Dose Study of BMS-986115 in Subjects With Advanced Solid TumorsRecruiting
CancerCA008-002A Phase I/IIa Study of BMS-986148 in Subjects With Select Advanced Solid TumorsNot yet recruiting
Cancer, Leukemia (Adult)CA180-330Studying First Line Treatment of Chronic Myeloid Leukemia (CML) in a Real-world SettingRecruiting
Cancer, Leukemia (Adult)CA180-373A Phase 1B Study to Investigate the Safety and Preliminary Efficacy for the Combination of Dasatinib Plus Nivolumab in Patients With Chronic Myeloid LeukemiaRecruiting
Cancer, Leukemia (Adult)CA180-399Phase IIb Study of Dasatinib Versus Imatinib in Patients With CML-CP Who Have Not Achieved an Early Optimal Response to ImatinibRecruiting
Cancer, Leukemia (Adult)CA180-400This Study Will be a Phase IV, Open-label, Multicenter Study of Dasatinib in Chronic-Phase Chronic Myeloid Leukemia (CP-CML) Patients With Chronic, Low-grade Non-Hematologic Toxicity to ImatinibRecruiting
Cancer, Leukemia (Adult)CA180-406Open-Label Study Evaluating Dasatinib Therapy Discontinuation in Patients With Chronic Phase Chronic Myeloid Leukemia With Stable Complete Molecular ResponseRecruiting
Cancer, MelanomaCA184-143A Multi-National, Prospective, Observational Study in Patients With Unresectable or Metastatic MelanomaRecruiting
Cancer, Melanoma (Pediatric), Pediatric StudiesCA184-178Phase 2 Study of Ipilimumab in Children and Adolescents (12 to < 18 Years) With Previously Treated or Untreated, Unresectable Stage III or Stage lV Malignant MelanomaRecruiting
CancerCA184-437Safety and Efficacy Study of Ipilimumab 3 mg/kg Versus Ipilimumab 10 mg/kg in Subjects With Metastatic Castration Resistant Prostate Cancer Who Are Chemotherapy NaiveRecruiting
Cancer, Solid TumorsCA186-011Safety, Tolerability, Pharmacokinetics, and Immunoregulatory Study of Urelumab (BMS-663513) in Subjects With Advanced and/or Metastatic Solid Tumors and Relapsed/Refractory B-cell Non-Hodgkin's LymphomaRecruiting
CancerCA186-017Combination Study of Urelumab and Rituximab in Patients With B-cell Non-Hodgkins LymphomaRecruiting
Colorectal Cancer, Gastrointestinal Cancer, CancerCA186-018Combination Study of Urelumab and Cetuximab in Patients With Advanced/Metastatic Colorectal Cancer or Advanced/Metastatic Head and Neck CancerRecruiting
CancerCA186-107Study of the Safety and Tolerability of Urelumab Administered in Combination With Nivolumab in Solid Tumors and B-cell Non-Hodgkins LymphomaRecruiting
Cancer, Leukemia (Adult), Multiple MyelomaCA204-008Prospective Research Assessment in Multiple Myeloma: An Observational Evaluation (PREAMBLE)Recruiting
Cancer, Leukemia (Adult), Multiple MyelomaCA204-009Study of Bortezomib and Dexamethasone With or Without Elotuzumab to Treat Relapsed or Refractory Multiple MyelomaRecruiting
Cancer, Leukemia (Adult), Multiple MyelomaCA204-112Study of Safety of Elotuzumab Administered Over Approximately 60 Minutes in Combination With Lenalidomide and Dexamethasone for Newly Diagnosed or Relapsed/Refractory Multiple Myeloma PatientsRecruiting
Lung Cancer, CancerCA209-012Study of Nivolumab (BMS-936558) in Combination With Gemcitabine/Cisplatin, Pemetrexed/Cisplatin, Carboplatin/Paclitaxel, Bevacizumab Maintenance, Erlotinib, Ipilimumab or as Monotherapy in Subjects With Stage IIIB/IV Non-small Cell Lung Cancer (NSCLC) (CheckMate 012)Recruiting
Lung Cancer, CancerCA209-026An Open-Label, Randomized, Phase 3 Trial of Nivolumab Versus Investigator's Choice Chemotherapy as First-Line Therapy for Stage IV or Recurrent PD-L1+ Non-Small Cell Lung Cancer (CheckMate 026)Recruiting
Cancer, Solid TumorsCA209-032A Phase 1/2, Open-label Study of Nivolumab Monotherapy or Nivolumab Combined With Ipilimumab in Subjects With Advanced or Metastatic Solid TumorsRecruiting
Cancer, Leukemia (Adult)CA209-039Safety Study in Nivolumab Alone and in Combination With Ipilimumab or Lirilumab in Lymphoma and Multiple MyelomaRecruiting
Liver Cancer, CancerCA209-040Study to Evaluate the Effectiveness, Safety and Tolerability of Nivolumab in Subjects With Advanced Liver Cancer Anti-PD-1 HCC (Anti-Programmed-Death-1 Hepatocellular Carcinoma)Recruiting
Lymphoma, Non Hodgkin's Lymphoma, Non Hodgkin's Lymphoma (DLBCL), CancerCA209-139Study of Nivolumab in Patients With Relapsed or Refractory Diffuse Large B-Cell Lymphoma (DLBCL) That Have Either Failed or Are Not Eligible for Autologous Stem Cell Transplant (CheckMate 139)Recruiting
Cancer, Lymphoma, Non Hodgkin's Lymphoma, Non Hodgkin's Lymphoma (Follicular)CA209-140Study of Nivolumab in Subjects With Relapsed or Refractory Follicular Lymphoma (FL) (CheckMate 140)Recruiting
Cancer, Head and Neck cancer (SCCHN)CA209-141Trial of Nivolumab vs Therapy of Investigator's Choice in Recurrent or Metastatic Head and Neck Carcinoma (CheckMate 141)Recruiting
Colorectal Cancer, Cancer, Colon Cancer MSI HighCA209-142A Study of Nivolumab and Nivolumab Plus Ipilimumab in Recurrent and Metastatic Colon Cancer (CheckMate 142)Recruiting
Glioblastoma, Brain CancerCA209-143A Randomized Study of Nivolumab Versus Bevacizumab and a Safety Study of Nivolumab in Adult Subjects With Recurrent Glioblastoma (GBM) (CheckMate 143)Recruiting
Cancer, Lung CancerCA209-153A Safety Trial of Nivolumab (BMS-936558) in Subjects With Advanced or Metastatic Non-Small Cell Lung Cancer Who Have Progressed During or After Receiving At Least One Prior Systemic Regimen (CheckMate 153)Recruiting
Cancer, MelanomaCA209-168Expanded Access Program With Nivolumab for Subjects With Histologically Confirmed Stage III (Unresectable) or Stage IV Melanoma Progressing Post Prior Systemic Treatment Containing an Anti_CTLA-4 Monoclonal Antibody (CheckMate 168)Available
Cancer, MelanomaCA209-204A Multi-Center Phase 2 Open-Label Study to Evaluate Safety and Efficacy in Subjects With Melanoma Metastatic to the Brain Treated With Nivolumab in Combination With Ipilimumab Followed by Nivolumab Monotherapy (CheckMate 204)Recruiting
Lymphoma, Hodgkin Lymphoma , CancerCA209-205Study of Nivolumab in Subjects With Hodgkin's Lymphoma (Registrational) (CheckMate 205)Recruiting
Kidney Cancer, Cancer, Renal Cell CarcinomaCA209-214Nivolumab Combined With Ipilimumab Versus Sunitinib in Previously Untreated Advanced or Metastatic Renal Cell Carcinoma (CheckMate 214)Recruiting
Cancer, MelanomaCA209-218Expanded Access Program With Nivolumab (BMS-936558) in Combination With Ipilimumab (Yervoy®) in Anti-CTLA-4 Treatment-Naïve Subjects With Unresectable or Metastatic Melanoma (CheckMate 218)Available
CancerCA209-275A Study of Nivolumab in Participants With Metastatic or Unresectable Bladder CancerRecruiting
Cancer, Solid TumorsCA216-001Study to Evaluate the Safety and Tolerability of IV Doses of BMS-906024 in Subjects With Advanced or Metastatic Solid TumorsRecruiting
Cancer, Leukemia (Adult), Non Hodgkin's Lymphoma, LymphomaCA216-002Study to Evaluate the Safety and Tolerability of Weekly Intravenous (IV) Doses of BMS-906024 in Subjects With Acute T-cell Lymphoblastic Leukemia or T-cell Lymphoblastic LymphomaRecruiting
CancerCA216-003Study to Evaluate Safety & Tolerability of BMS-906024 in Combination With Chemotherapy & to Define DLTs & MTD of BMS-906024 in Combination With One of the Following Chemotherapy Regimens; Weekly Paclitaxel, 5FU+Irinotecan or Carboplatin+Paclitaxel in Subjects With Advanced / Metastatic Solid TumorsRecruiting
Cancer, Solid TumorsCA223-001A Phase I Study of an Anti-KIR Antibody in Combination With an Anti-PD1 Antibody in Patients With Advanced Solid TumorsRecruiting
Cancer, Leukemia (Adult)CA223-028A Phase I Open Label Study of the Safety and Tolerability of Elotuzumab (BMS-901608) Administered in Combination With Either Lirilumab (BMS-986015) or Urelumab (BMS-663513) in Subjects With Multiple MyelomaRecruiting
CancerCA224-020Safety Study of Anti-LAG-3 With and Without Anti-PD-1 in the Treatment of Solid TumorsRecruiting
CancerCA224-022Safety Study of Anti-LAG-3 in CLL, HL, NHL and MMRecruiting
 CN001-001Placebo-Controlled, Single and Multiple Ascending Subcutaneous Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of BMS-986089 in Healthy Adult SubjectsRecruiting
 CN002-001A Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Study of Intravenously Administered BMS-986168 in Healthy SubjectsRecruiting
 CV004-006Multiple Ascending Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics of BMS-986120 in Healthy Subjects and the Effects of Co-Administration of Midazolam and BMS-986120Recruiting
 CV006-003Single and Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of BMS-986141 in Healthy SubjectsRecruiting
Diabetes (Pediatric), Pediatric StudiesCV181-058Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of Saxagliptin as Monotherapy in Pediatric Patients With Type 2 DiabetesRecruiting
Diabetes (Pediatric), Pediatric StudiesCV181-147A Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Saxagliptin (BMS-477118) in Combination With Metformin IR or Metformin XR in Pediatric Patients With Type 2 Diabetes Who Have Inadequate Glycemic Control on Metformin AloneRecruiting
Diabetes (Adult)CV181-206Phase 4: Investigational Study to Evaluate Metformin XR Monotherapy Versus Metformin IR Monotherapy in Subjects With Type 2 DiabetesRecruiting
Diabetes (Adult)CV181-363Study to Evaluate the Efficacy and Safety of Saxagliptin Co-administered With Dapagliflozin in Combination With Metformin Compared to Sitagliptin in Combination With Metformin in Adult Patients With Type 2 Diabetes Who Have Inadequate Glycemic Control on Metformin Therapy AloneRecruiting
Blood Clots (Pediatric)CV185-118Study to Evaluate a Single Dose of Apixaban in Pediatric Subjects at Risk for a Thrombotic DisorderRecruiting
Diabetes (Adult), Kidney DiseaseCV202-010Study to Evaluate the Effects of BMS-813160 on Protein Loss in the Urine of Subjects With Type 2 Diabetes and Diabetic Kidney DiseaseRecruiting
 CV205-005A Blinded Study to Evaluate Effect on Atrial Fibrillation Burden in Patients With Paroxysmal Atrial FibrillationRecruiting
Rheumatoid ArthritisIM001-001A Randomized, Placebo-Controlled, Double-Blind, Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of BMS-986104 in Healthy Male SubjectsRecruiting
 IM006-001Study to Evaluate the Safety, Pharmacokinetics and Target Engagement of BMS-986142 in Healthy SubjectsRecruiting
Rheumatoid ArthritisIM101-121Abatacept Pregnancy Exposure RegistryRecruiting
Rheumatoid ArthritisIM101-240An Observational Registry of Abatacept in Patients With Juvenile Idiopathic ArthritisRecruiting
Lupus, Lupus NephritisIM101-291Efficacy and Safety Study of Abatacept to Treat Lupus NephritisRecruiting
Rheumatoid Arthritis, Pediatric StudiesIM101-301Pharmacokinetics, Efficacy and Safety of Abatacept Administered Subcutaneously (SC) in Children and Adolescents With Active Polyarticular Juvenile Idiopathic Arthritis (pJIA) and Inadequate Response (IR) to Biologic or Non Biologic Disease Modifying Anti-rheumatic Drugs (DMARDs)Recruiting
TransplantationIM103-076Evaluating Nulojix (Belatacept) Long-Term Safety in TransplantRecruiting
TransplantationIM103-116A Study in Maintenance Kidney Transplant Recipients Following Conversion to Nulojix® (Belatacept)-BasedRecruiting
Renal Transplant (Pediatric), Pediatric StudiesIM103-144Phase II Pharmacokinetics, Efficacy, and Safety of Belatacept in Pediatric Renal Transplant RecipientsRecruiting
LupusIM128-027Safety and Efficacy Study of a Biologic to Treat Systemic Lupus ErythematosusRecruiting
Idiopathic Pulmonary Fibrosis, Lung DiseaseIM136-003Safety and Efficacy of a Lysophosphatidic Acid Receptor Antagonist in Idiopathic Pulmonary FibrosisRecruiting
Idiopathic Thrombocytopenia Purpura (ITP), ITPIM140-103Study to Evaluate Safety and Efficacy in Adult Subjects With ITPRecruiting
 IM142-003Study to Evaluate the Safety, Tolerability, PK, and PD of BMS-986090 in Healthy SubjectsRecruiting
 MB006-002Randomized, Placebo-Controlled, Double-Blind, Ascending Single and Multiple Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics of BMS-963272 in Healthy SubjectsRecruiting
Diabetes (Adult)MB102-229Efficacy and Safety Study of Dapagliflozin in Type 1 DiabetesRecruiting
Diabetes (Adult)MB130-002A Study to Evaluate BMS-986036 in Obese Adults With Type-2 DiabetesRecruiting