COMPANY
Bristol-Myers Squibb
FDA-approved therapeutic company FDA-cleared device company Clinical Phase 3
Bristol Myers Squibb is a global biopharmaceutical company. From company website Source · Oct 12, 2026
Hiring
| Title | Location (from posting) | Employer posted | First seen |
|---|---|---|---|
| Cybersecurity Specialist II - Application Security | Hyderabad - TS - IN | Oct 22, 2026 | Oct 13, 2026 |
| Clinical Trial Results Manager | Hyderabad - TS - IN | Oct 22, 2026 | Oct 22, 2026 |
| Clinical Trial Registration Manager II | Hyderabad - TS - IN | Oct 22, 2026 | Oct 22, 2026 |
| Risk Analyst II | Hyderabad - TS - IN | Oct 22, 2026 | Oct 22, 2026 |
| Speciality Care Advisor (Field based in Delhi) | Field - India - IN | Oct 22, 2026 | Oct 22, 2026 |
Trial and FDA signals
- New trial + clinical hiring Started a Phase 3 trial (NCT07680790, actual start Sep 8, 2026) (+5 other new trials); 73 clinical-operations roles open. ClinicalTrials.gov NCT07680790 (Sep 8, 2026)
Evidence (6 events)
- Sep 8, 2026 · ClinicalTrials.gov NCT07680790
leadSponsor.name='Bristol-Myers Squibb'; phases=['PHASE3']; overallStatus=RECRUITING; startDateStruct={date:2026-09-08,type:ACTUAL}; studyFirstPostDate=2026-07-02; briefTitle='Study of Izalontamab Brengitecan (BMS-986507) in Combination With Osimertinib Versus Osimertinib Monotherapy or Osimertinib in Combination W' - Sep 10, 2026 · ClinicalTrials.gov NCT07680764
leadSponsor.name='Bristol-Myers Squibb'; phases=['PHASE2']; overallStatus=RECRUITING; startDateStruct={date:2026-09-10,type:ACTUAL}; studyFirstPostDate=2026-07-02; briefTitle='A Study To Assess the Safety, Tolerability, and Efficacy of Imzokitug in Combination With Pumitamig and Platinum-Doublet Chemotherapy (PDCT)' - Jul 27, 2026 · ClinicalTrials.gov NCT07492680
leadSponsor.name='Bristol-Myers Squibb'; phases=['PHASE2']; overallStatus=RECRUITING; startDateStruct={date:2026-07-27,type:ACTUAL}; studyFirstPostDate=2026-03-25; briefTitle='A Study of BMS-986504 Monotherapy and in Combination With Other Agents in Participants With Advanced and/or Metastatic Solid Tumors With Hom' - Sep 8, 2026 · ClinicalTrials.gov NCT07763418
leadSponsor.name='Bristol-Myers Squibb'; phases=['PHASE1']; overallStatus=RECRUITING; startDateStruct={date:2026-09-08,type:ACTUAL}; studyFirstPostDate=2026-08-13; briefTitle='A Study to Evaluate the Pharmacokinetics and Safety of Golcadomide in Participants With Severe Renal Impairment and End-Stage Renal Disease ' - Aug 31, 2026 · ClinicalTrials.gov NCT07800897
leadSponsor.name='Bristol-Myers Squibb'; phases=['PHASE1']; overallStatus=RECRUITING; startDateStruct={date:2026-08-31,type:ACTUAL}; studyFirstPostDate=2026-09-02; briefTitle='A Study of Navlimetostat (BMS-986504) Drug Interactions and Food Effect in Healthy Participants' - Aug 21, 2026 · ClinicalTrials.gov NCT07780383
leadSponsor.name='Bristol-Myers Squibb'; phases=['PHASE1']; overallStatus=RECRUITING; startDateStruct={date:2026-08-21,type:ACTUAL}; studyFirstPostDate=2026-08-21; briefTitle='A Study to Evaluate the Drug Levels, Absolute Bioavailability, Safety, Tolerability, and Immunogenicity of Single-Dose of BMS-986446 in Heal'
- Sep 8, 2026 · ClinicalTrials.gov NCT07680790
- Drug approval + hiring FDA novel approval for ZENBEXUS (NDA 221075, Aug 13, 2026); 378 manufacturing/quality or commercial roles open. FDA NDA 221075 (Aug 13, 2026)
Evidence (1 event)
- Aug 13, 2026 · FDA NDA 221075
openFDA drugsfda: application_number=NDA221075; sponsor_name='BRISTOL MYERS SQUIBB'; submission_type=ORIG; submission_number=1; submission_status=AP; submission_status_date=20260813; submission_class_code=TYPE 1; brand_name=['ZENBEXUS']
- Aug 13, 2026 · FDA NDA 221075
Timeline
- Trial start Phase 1: Study to Assess Drug Levels, Immune Response, Safety and Tolerability of BMS-986446 in Healthy Chinese Participants. source ↗
- Trial start —: Repotrectinib Post-Marketing Surveillance in Korean Patients With ROS1-Positive Non-Small Cell Lung Cancer (NSCLC) or Solid Tumors Harboring a Neurotrophic Tyrosine Receptor Kinase (NTRK) Gene Fusi source ↗
- Board tracked Radar started tracking this company’s job board (739 open jobs at last check). source ↗
- Trial start Phase 3: A Study of KarXT + KarX-EC for Treatment of Irritability in Children and Adolescents With Autism Spectrum Disorder source ↗
- FDA FDA New indication / efficacy supplement: CAMZYOS (mavacamten) — NDA214998/13, Sep 30, 2026. Applicant at approval: Bristol-Myers Squibb Company. source ↗
- Trial start —: Evaluation of Mavacamten-Based Practice in Chinese Adults With Obstructive Hypertrophic Cardiomyopathy source ↗
- Trial start Phase 2: A Study To Assess the Safety, Tolerability, and Efficacy of Imzokitug in Combination With Pumitamig and Platinum-Doublet Chemotherapy (PDCT) Versus Pumitamig and PDCT as First-line Treatment source ↗
- Trial start Phase 3: Study of Izalontamab Brengitecan (BMS-986507) in Combination With Osimertinib Versus Osimertinib Monotherapy or Osimertinib in Combination With Platinum-based Chemotherapy for EGFRmt Non-smal source ↗
- Trial start Phase 1: A Study to Evaluate the Pharmacokinetics and Safety of Golcadomide in Participants With Severe Renal Impairment and End-Stage Renal Disease Compared With Participants With Normal Renal Functi source ↗
- Trial start Phase 1: A Study of Navlimetostat (BMS-986504) Drug Interactions and Food Effect in Healthy Participants source ↗
- Trial start Phase 1: A Study to Evaluate the Drug Levels, Absolute Bioavailability, Safety, Tolerability, and Immunogenicity of Single-Dose of BMS-986446 in Healthy Adults After Single-dose Administration, and Pa source ↗
- FDA FDA New drug/biologic (novel): ZENBEXUS (iberdomide hydrochloride) — NDA221075, Aug 13, 2026. Applicant at approval: Bristol-Myers Squibb Company. Accelerated approval. source ↗
- Trial start —: Asia Myelodysplastic Syndrome (MDS) Registry source ↗
- Trial start Phase 2: A Study of BMS-986504 Monotherapy and in Combination With Other Agents in Participants With Advanced and/or Metastatic Solid Tumors With Homozygous MTAP Deletion (MountainTAP-5) source ↗
- Trial start —: First-Line Systemic Therapies in Advanced Renal Cell Carcinoma in Spain source ↗
- Trial start 1: A Phase 1 Study of Navlimetostat Tablet Formulations source ↗
- FDA FDA New indication / efficacy supplement: ONUREG (azacitidine) — NDA214120/3, Apr 9, 2026. Applicant at approval: Bristol-Myers Squibb Company. source ↗
- Trial start Phase 1/Phase 2: A Study to Evaluate the Safety, Tolerability, and Efficacy of Pumitamig Alone or in Combination With Other Agents in Participants With Advanced Renal Cell Carcinoma (RCC) (ROSETTA RCC source ↗
- FDA FDA New indication / efficacy supplement: OPDIVO (nivolumab) — BLA125554/135, Mar 20, 2026. Applicant at approval: Bristol-Myers Squibb Company. source ↗
- Trial start Phase 3: A Study to Evaluate Pumitamig Versus Durvalumab Following Concurrent Chemoradiation Therapy in Participants With Unresectable Stage III Non-small Cell Lung Cancer (NSCLC) (ROSETTA Lung-201) source ↗
- Trial start Phase 1/Phase 2: A Study to Evaluate the Safety and Tolerability of Pumitamig Alone or In Combination With Ipilimumab in Participants With First-Line Advanced or Unresectable Hepatocellular Carcinoma source ↗
- Trial start Phase 2/Phase 3: A Study to Evaluate the Safety and Efficacy of Pumitamig in Combination With Chemotherapy Versus Nivolumab in Combination With Chemotherapy in Participants With Previously Untreated A source ↗
- Trial start Phase 3: A Study to Evaluate the Efficacy of Pumitamig Versus Pembrolizumab in Participants With Previously Untreated Advanced Non-Small Cell Lung Cancer and PD-L1 ≥ 50%. (ROSETTA Lung-202) source ↗
- FDA FDA New indication / efficacy supplement: SOTYKTU (deucravacitinib) — NDA214958/2, Mar 6, 2026. Applicant at approval: Bristol Myers Squibb Company. source ↗
- Trial start Phase 1: A Study to Evaluate the Safety, Tolerability, and Drug Levels of BMS-986454 in Participants With Rheumatoid Arthritis source ↗
Upcoming milestones
- Oct 31, 2026 (ESTIMATED) · · Asia Myelodysplastic Syndrome (MDS) Registry · NCT07355478
- Nov 2, 2026 (ESTIMATED) · 1 · A Phase 1 Study of Navlimetostat Tablet Formulations · NCT07544628
- Nov 2, 2026 (ESTIMATED) · Phase 3 · A Study to Evaluate the Efficacy and Safety of KarXT for the Treatment of Manic Episodes in Bipolar-I Disorder (BALSAM-2) · NCT06951711
- Dec 14, 2026 (ESTIMATED) · Phase 1 · A Study to Evaluate the Pharmacokinetics and Safety of Golcadomide in Participants With Severe Renal Impairment and End-Stage Renal Disease Compared With Participants With Normal Renal Function · NCT07763418
- Mar 25, 2027 (ESTIMATED) · Phase 1 · A Study of Navlimetostat (BMS-986504) Drug Interactions and Food Effect in Healthy Participants · NCT07800897
- Mar 31, 2027 (ESTIMATED) · · Evaluation of Mavacamten-Based Practice in Chinese Adults With Obstructive Hypertrophic Cardiomyopathy · NCT07846059
- Jun 17, 2027 (ESTIMATED) · Phase 1 · A Study to Evaluate the Drug Levels, Absolute Bioavailability, Safety, Tolerability, and Immunogenicity of Single-Dose of BMS-986446 in Healthy Adults After Single-dose Administration, and Participant · NCT07780383
- Jun 28, 2027 (ESTIMATED) · Phase 1 · A Study to Evaluate the Safety, Tolerability, and Drug Levels of BMS-986454 in Participants With Rheumatoid Arthritis · NCT07171983
Open jobs 732
| Title | Location (from posting, not HQ) | Employer posted | First seen | Level |
|---|---|---|---|---|
| Cybersecurity Specialist II - Application Security | Hyderabad - TS - IN | Oct 22, 2026 | Oct 13, 2026 | Not stated |
| Clinical Trial Results Manager | Hyderabad - TS - IN | Oct 22, 2026 | Oct 22, 2026 | Not stated |
| Clinical Trial Registration Manager II | Hyderabad - TS - IN | Oct 22, 2026 | Oct 22, 2026 | Not stated |
| Risk Analyst II | Hyderabad - TS - IN | Oct 22, 2026 | Oct 22, 2026 | Not stated |
| Speciality Care Advisor (Field based in Delhi) | Field - India - IN | Oct 22, 2026 | Oct 22, 2026 | Not stated |
| EMEA Payroll Analyst | Warsaw - PL | Oct 22, 2026 | Oct 22, 2026 | Not stated |
| Senior Manager I, Advanced Capabilities COE | Hyderabad - TS - IN | Oct 22, 2026 | Oct 22, 2026 | Not stated |
| Senior Analyst (Business Analyst II) | Hyderabad - TS - IN | Oct 22, 2026 | Oct 22, 2026 | Not stated |
| Director, Biostatistics | 3 locations, including US, NJ, Giralda, Madison | Oct 22, 2026 | Oct 22, 2026 | Not stated |
| Specialist, APAC Site Accounts, Scheduling & Cell Logistics | Otemachi-JP | Oct 22, 2026 | Oct 22, 2026 | Not stated |
| Senior Manager, Health Economics & Outcomes Research (HEOR) | Otemachi-JP | Oct 22, 2026 | Oct 22, 2026 | Not stated |
| Manager, Technical Lead, Sterile Drug Product (Manufacturing) | Cruiserath - IE | Oct 21, 2026 | Oct 7, 2026 | Senior |
| Associate, QC Analytical, Cell Therapy | Devens - MA - US | Oct 21, 2026 | Oct 7, 2026 | Not stated |
| Sr. Manager, Marketing and Commercialization Capability Development, Commercialization Learning Japancialization Learning Japan | Otemachi-JP | Oct 21, 2026 | Oct 7, 2026 | Senior |
| Executive Director, Research – Integrative Sciences — Cardiovascular | 2 locations, including US, MA, Cambridge Crossing | Oct 21, 2026 | Oct 7, 2026 | Executive |
| Sr. Medical Information Communication Specialist, IO | Nanjing - CN | Oct 21, 2026 | Oct 7, 2026 | Mid |
| Director, Drug Development AI Nexus Decision Integration Lead | 4 locations, including US, NJ, Princeton | Oct 21, 2026 | Oct 7, 2026 | Senior |
| Senior Therapeutic Area Specialist, Cardiovascular Community - Lafayette, IN/Northwest Indiana | 2 locations, including US, IN, Lafayette | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Executive Director, Chief of Staff, Global Development Operations | 2 locations, including CH, Boudry | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Director - US Field HEOR Scientist | Field - United States - US | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Associate Director, Customer Insights & Engagement, Lung Cancer | Princeton - NJ - US | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Associate Director, Aseptic Facility and Utility Design | 7 locations, including US, NJ, New Brunswick | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Associate Director, Clinical Pharmacology | Princeton - NJ - US | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Senior Manager Biospecimen Lead | 2 locations, including US, NJ, Princeton | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Electrician | Devens - MA - US | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Senior Specialist, Field Quality QA Operations | Devens - MA - US | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Associate Scientist | Seattle, WA | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Associate Director, Portfolio Consolidation | Princeton - NJ - US | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Senior Scientist, Gene Delivery and Editing Process Development | Seattle, WA | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Director, ASAT Critical Reagent Operations | 3 locations, including US, MA, Devens | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| International Therapeutic Area Head Immunology/Cardiovascular | 8 locations, including CH, Boudry | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Director, Global Clinical Trial Physician | 2 locations, including GB, Uxbridge | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Senior Technician, Clinical Supply Warehouse & Logistics Operations | Moreton - GB | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Manager, Operations Supply Planner | 2 locations, including Dublin, EXMFG | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Manager, Quality Engineering, Change Control/Document Review | Madison - Giralda - NJ - US | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Senior Manager, QA Engineering (Equipment/Lab Methods/Utilities/Facilities) | Madison - Giralda - NJ - US | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Senior Manufacturing Associate, Cell Therapy in Devens, MA | Devens - MA - US | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Senior Manufacturing Associate, Cell Therapy in Devens, MA | Devens - MA - US | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Drug Product Associate, Sterile Drug Product | Cruiserath - IE | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Senior Specialist, Submission Management | Warsaw - PL | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Manager, Submission Management | Warsaw - PL | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Therapeutic Area Specialist, Hematology & Oncology (m/f/d) - Gebiet 10303: Heidelberg, Mannheim, Heilbronn, Freiburg | 4 locations, including DE, Germany, Field | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Scientist | New Brunswick - NJ - US | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Senior Specialist, QCAS Instrumentation | Cruiserath - IE | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Senior Manager, Regulatory Sciences (m/w/d) | Munich - DE | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Therapeutic Area Specialist Immunology | Field - Poland - PL | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Senior Manager, Content Strategy & Enablement | Otemachi-JP | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Global Trial Acceleration Associate | Hyderabad - TS - IN | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| IO Medical Information Communication Specialist | Jinan - CN | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| 2027 Summer Intern Real Estate | Princeton - NJ - US | Oct 20, 2026 | Oct 7, 2026 | Entry |
Clinical trials (lead sponsor) Showing 50 of 1,560
| Record | Title | Phase | Status | Start | Primary completion |
|---|---|---|---|---|---|
| NCT07680790 | Study of Izalontamab Brengitecan (BMS-986507) in Combination With Osimertinib Versus Osimertinib Monotherapy or Osimertinib in Combination With Platinum-based Chemotherapy for EGFRmt Non-small Cell Lung Cancer (IZABRIGHT-Lung02) | Phase 3 | Recruiting | Sep 8, 2026 | Dec 30, 2031 (estimated) |
| NCT06976203 | A Study to Evaluate the Efficacy and Safety of KarXT + KarX-EC for Cognitive Impairment in Alzheimer's Disease (MINDSET 2) | Phase 3 | Recruiting | Jul 21, 2025 | Sep 11, 2028 (estimated) |
| NCT07355478 | Asia Myelodysplastic Syndrome (MDS) Registry | Not listed | Recruiting | Aug 11, 2026 | Oct 31, 2026 (estimated) |
| NCT07011745 | A Phase 3 Study to Evaluate the Safety and Efficacy of KarXT + KarX-EC for the Treatment of Agitation Associated With Alzheimer's Disease | 3 | Recruiting | Jul 16, 2025 | Nov 3, 2028 (estimated) |
| NCT06035497 | A Study to Assess the Safety, Tolerability, Efficacy, and Drug Levels of BMS-986369 (Golcadomide) in Participants With Relapsed or Refractory T-cell Lymphomas in Japan (GOLSEEK-3) | Phase 1/Phase 2 | Active, not recruiting | Nov 20, 2023 | Aug 11, 2026 (actual) |
| NCT07544628 | A Phase 1 Study of Navlimetostat Tablet Formulations | 1 | Recruiting | Apr 27, 2026 | Nov 2, 2026 (estimated) |
| NCT06976216 | A Study to Evaluate the Efficacy and Safety of KarXT + KarX-EC for Cognitive Impairment in Alzheimer's Disease | Phase 3 | Recruiting | Jul 14, 2025 | Sep 11, 2028 (estimated) |
| NCT07492680 | A Study of BMS-986504 Monotherapy and in Combination With Other Agents in Participants With Advanced and/or Metastatic Solid Tumors With Homozygous MTAP Deletion (MountainTAP-5) | Phase 2 | Recruiting | Jul 27, 2026 | Aug 15, 2028 (estimated) |
| NCT00724334 | A Long-Term Study of the Effects of Orally Administered SAR302503 in Patients With Myelofibrosis | Phase 1/Phase 2 | Completed | Jul 31, 2008 | May 28, 2014 (actual) |
| NCT06997029 | A Phase 1 Study of BMS-986500 as Monotherapy or Combination Therapy in Advanced Solid Tumors | 1 | Recruiting | Aug 1, 2025 | Dec 14, 2028 (estimated) |
| NCT07288567 | A Study to Evaluate the Efficacy and Safety of KarXT for the Treatment of Schizophrenia in Adolescents (EMERGENT TEEN) | Phase 3 | Recruiting | Jan 29, 2026 | Dec 18, 2029 (estimated) |
| NCT06869551 | A Study to Evaluate the Drug Levels, Efficacy, and Safety of Deucravacitinib (BMS-986165) in Pediatric Participants With Juvenile Psoriatic Arthritis | Phase 3 | Recruiting | Mar 13, 2025 | Mar 6, 2030 (estimated) |
| NCT07800897 | A Study of Navlimetostat (BMS-986504) Drug Interactions and Food Effect in Healthy Participants | Phase 1 | Recruiting | Aug 31, 2026 | Mar 25, 2027 (estimated) |
| NCT07680764 | A Study To Assess the Safety, Tolerability, and Efficacy of Imzokitug in Combination With Pumitamig and Platinum-Doublet Chemotherapy (PDCT) Versus Pumitamig and PDCT as First-line Treatment for Participants With Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC) | Phase 2 | Recruiting | Sep 10, 2026 | Sep 15, 2028 (estimated) |
| NCT07017699 | A Study to Assess Deucravacitinib Safety in Pregnancy | Not listed | Recruiting | Mar 21, 2025 | Apr 1, 2028 (estimated) |
| NCT07465029 | A Study of Incidence, Treatment Patterns, and Outcomes in Transfusion-dependent Lower-risk Myelodysplastic Syndromes in Spain | Not listed | Active, not recruiting | Feb 2, 2026 | Apr 23, 2026 (actual) |
| NCT06952465 | A Study Comparing the Risk of Serious Infections and Malignancies With Deucravacitinib or Biologics in Japanese Patients With Psoriasis | Not listed | Active, not recruiting | Jan 24, 2025 | Nov 30, 2031 (estimated) |
| NCT07458542 | Effectiveness and Safety of ONUREG (Oral Azacitidine) in Chinese Patients With Acute Myeloid Leukemia | Not listed | Completed | Dec 9, 2025 | Jan 9, 2026 (actual) |
| NCT07171983 | A Study to Evaluate the Safety, Tolerability, and Drug Levels of BMS-986454 in Participants With Rheumatoid Arthritis | Phase 1 | Recruiting | Feb 27, 2026 | Jun 28, 2027 (estimated) |
| NCT07852962 | Study to Assess Drug Levels, Immune Response, Safety and Tolerability of BMS-986446 in Healthy Chinese Participants. | Phase 1 | Not yet recruiting | Feb 10, 2027 | Jul 18, 2027 (estimated) |
| NCT06698887 | A Study to Evaluate the Long-Term Safety of Idecabtagene Vicleucel Treatment in Adults With Newly Diagnosed Multiple Myeloma in Korea | Not listed | Recruiting | Sep 11, 2024 | Mar 27, 2031 (estimated) |
| NCT07571148 | Real-world Patient Characteristics, Treatment Patterns, and Healthcare Utilization Among KarXT Users | Not listed | Completed | Jan 16, 2026 | Mar 25, 2026 (actual) |
| NCT07852884 | First-Line Systemic Therapies in Advanced Renal Cell Carcinoma in Spain | Not listed | Active, not recruiting | Jul 15, 2026 | Sep 1, 2026 (actual) |
| NCT06419634 | Study of BMS-986497 (ORM-6151) as a Monotherapy, in Double and Triple Combination With Azacitidine and Venetoclax in Participants With Relapsed or Refractory Acute Myeloid Leukemia or Myelodysplastic Syndrome | Phase 1 | Terminated | May 29, 2024 | Aug 28, 2026 (actual) |
| NCT07763418 | A Study to Evaluate the Pharmacokinetics and Safety of Golcadomide in Participants With Severe Renal Impairment and End-Stage Renal Disease Compared With Participants With Normal Renal Function | Phase 1 | Recruiting | Sep 8, 2026 | Dec 14, 2026 (estimated) |
| NCT07599007 | Repotrectinib Post-Marketing Surveillance in Korean Patients With ROS1-Positive Non-Small Cell Lung Cancer (NSCLC) or Solid Tumors Harboring a Neurotrophic Tyrosine Receptor Kinase (NTRK) Gene Fusion | Not listed | Not yet recruiting | Oct 31, 2026 | Dec 30, 2027 (estimated) |
| NCT07361497 | A Study to Evaluate Pumitamig Versus Durvalumab Following Concurrent Chemoradiation Therapy in Participants With Unresectable Stage III Non-small Cell Lung Cancer (NSCLC) (ROSETTA Lung-201) | Phase 3 | Recruiting | Mar 16, 2026 | Sep 18, 2030 (estimated) |
| NCT07221149 | A Study to Evaluate the Safety and Efficacy of Pumitamig in Combination With Chemotherapy Versus Nivolumab in Combination With Chemotherapy in Participants With Previously Untreated Advanced or Metastatic Gastric, Gastroesophageal Junction, or Esophageal Adenocarcinoma (ROSETTA Gastric-204) | Phase 2/Phase 3 | Recruiting | Mar 13, 2026 | Nov 8, 2030 (estimated) |
| NCT06372457 | COLLIGO-HCM: A Multinational Observational Study of the Real-World Effectiveness of Mavacamten Among Patients With Symptomatic Obstructive Hypertrophic Cardiomyopathy (oHCM) | Not listed | Active, not recruiting | Dec 1, 2023 | Sep 29, 2025 (actual) |
| NCT07101094 | Evaluation of Treatment Satisfaction and KarXT Utilization Registry (RESKU) | Not listed | Recruiting | Sep 22, 2025 | Jan 31, 2029 (estimated) |
| NCT07107373 | A Study to Assess the Treatment of Obstructive Hypertrophic Cardiomyopathy (oHCM) With Mavacamten in the US | Not listed | Active, not recruiting | Dec 22, 2023 | Jul 26, 2024 (actual) |
| NCT06971185 | A Study to Evaluate Treatment Patterns and Effectiveness of Luspatercept | Not listed | Completed | Nov 22, 2024 | Aug 1, 2025 (actual) |
| NCT07361510 | A Study to Evaluate the Efficacy of Pumitamig Versus Pembrolizumab in Participants With Previously Untreated Advanced Non-Small Cell Lung Cancer and PD-L1 ≥ 50%. (ROSETTA Lung-202) | Phase 3 | Recruiting | Mar 12, 2026 | Oct 14, 2031 (estimated) |
| NCT07846059 | Evaluation of Mavacamten-Based Practice in Chinese Adults With Obstructive Hypertrophic Cardiomyopathy | Not listed | Not yet recruiting | Sep 30, 2026 | Mar 31, 2027 (estimated) |
| NCT07285798 | A Study of KarXT + KarX-EC for Treatment of Irritability in Children and Adolescents With Autism Spectrum Disorder | Phase 3 | Not yet recruiting | Oct 2, 2026 | Aug 6, 2029 (estimated) |
| NCT06937229 | A Study to Evaluate the Long-term Efficacy and Safety of KarXT + KarX-EC for Agitation in Alzheimer's Disease (ADAGIO-3) | Phase 3 | Recruiting | Dec 2, 2025 | Jun 22, 2029 (estimated) |
| NCT04908202 | A Study to Determine the Efficacy and Safety of Deucravacitinib Compared With Placebo in Participants With Active Psoriatic Arthritis (PsA) Who Are Naïve to Biologic Disease-modifying Anti-rheumatic Drugs | Phase 3 | Active, not recruiting | Jul 13, 2021 | Sep 5, 2024 (actual) |
| NCT06951711 | A Study to Evaluate the Efficacy and Safety of KarXT for the Treatment of Manic Episodes in Bipolar-I Disorder (BALSAM-2) | Phase 3 | Recruiting | Jun 13, 2025 | Nov 2, 2026 (estimated) |
| NCT05552976 | A Study to Evaluate Mezigdomide in Combination With Carfilzomib and Dexamethasone (MeziKD) Versus Carfilzomib and Dexamethasone (Kd) in Participants With Relapsed or Refractory Multiple Myeloma (SUCCESSOR-2) | Phase 3 | Active, not recruiting | Jan 10, 2023 | Sep 28, 2026 (estimated) |
| NCT05076175 | A Study Investigating Oral Ozanimod (RPC1063) in Pediatric Participants With Moderate to Severe Active Ulcerative Colitis | Phase 2/Phase 3 | Recruiting | May 30, 2022 | Jul 12, 2032 (estimated) |
| NCT07780383 | A Study to Evaluate the Drug Levels, Absolute Bioavailability, Safety, Tolerability, and Immunogenicity of Single-Dose of BMS-986446 in Healthy Adults After Single-dose Administration, and Participants With Early Alzheimer's Disease After Multiple Dose Administration | Phase 1 | Recruiting | Aug 21, 2026 | Jun 17, 2027 (estimated) |
| NCT06799286 | A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of BMS-986489 in Chinese Participants With Relapsed/Refractory Small Cell Lung Cancer | Phase 1 | Completed | May 7, 2025 | Sep 9, 2026 (actual) |
| NCT03899155 | Pan Tumor Rollover Study | Phase 2 | Recruiting | Aug 9, 2019 | Aug 25, 2029 (estimated) |
| NCT07293351 | A Study to Evaluate the Safety, Tolerability, and Efficacy of Pumitamig Alone or in Combination With Other Agents in Participants With Advanced Renal Cell Carcinoma (RCC) (ROSETTA RCC-208) | Phase 1/Phase 2 | Recruiting | Mar 26, 2026 | Nov 28, 2029 (estimated) |
| NCT07063745 | A Study to Compare the Combination of Navlimetostat (BMS-986504) With Pembrolizumab and Chemotherapy Versus Placebo Plus Pembrolizumab and Chemotherapy in First-line Metastatic Non-small Cell Lung Cancer Participants With Homozygous MTAP Deletion | Phase 2/Phase 3 | Recruiting | Jan 2, 2026 | Aug 12, 2031 (estimated) |
| NCT07221357 | A Study to Evaluate the Safety and Efficacy of Pumitamig in Combination With Chemotherapy Versus Bevacizumab in Combination With Chemotherapy in Participants With Previously Untreated, Unresectable, or Metastatic Colorectal Cancer | Phase 2/Phase 3 | Recruiting | Dec 31, 2025 | Feb 2, 2030 (estimated) |
| NCT06618287 | A Study to Evaluate the Safety, Tolerability, Drug Levels, and Preliminary Efficacy of BMS-986507 Combinations in Adult Participants With Advanced Solid Tumors | Phase 1/Phase 2 | Recruiting | Feb 4, 2025 | Feb 26, 2031 (estimated) |
| NCT07291076 | A Study to Evaluate the Safety and Tolerability of Pumitamig Alone or In Combination With Ipilimumab in Participants With First-Line Advanced or Unresectable Hepatocellular Carcinoma (HCC) (ROSETTA HCC-206) | Phase 1/Phase 2 | Recruiting | Mar 16, 2026 | Oct 15, 2029 (estimated) |
| NCT06561386 | A Study to Compare the Efficacy of Nivolumab and Relatlimab Plus Chemotherapy vs Pembrolizumab Plus Chemotherapy for Stage IV/Recurrent Non-squamous Non-small Cell Lung Cancer With PD-L1 Expression ≥ 1% | Phase 3 | Recruiting | Oct 7, 2024 | Jul 30, 2030 (estimated) |
| NCT07100080 | Study of Izalontamab Brengitecan (BMS-986507) Versus Platinum-Pemetrexed for EGFR-mutated Non-small Cell Lung Cancer After Failure of EGFR TKI Therapy (IZABRIGHT-Lung01) | Phase 2/Phase 3 | Recruiting | Nov 5, 2025 | Dec 15, 2028 (estimated) |
FDA records (last 2 years)
- FDA New indication / efficacy supplement: CAMZYOS (mavacamten) — NDA214998/13, Sep 30, 2026. Applicant at approval: Bristol-Myers Squibb Company. source ↗
- FDA New drug/biologic (novel): ZENBEXUS (iberdomide hydrochloride) — NDA221075, Aug 13, 2026. Applicant at approval: Bristol-Myers Squibb Company. Accelerated approval. source ↗
- FDA New indication / efficacy supplement: ONUREG (azacitidine) — NDA214120/3, Apr 9, 2026. Applicant at approval: Bristol-Myers Squibb Company. source ↗
- FDA New indication / efficacy supplement: OPDIVO (nivolumab) — BLA125554/135, Mar 20, 2026. Applicant at approval: Bristol-Myers Squibb Company. source ↗
- FDA New indication / efficacy supplement: SOTYKTU (deucravacitinib) — NDA214958/2, Mar 6, 2026. Applicant at approval: Bristol Myers Squibb Company. source ↗
- FDA New indication / efficacy supplement: OPDIVO QVANTIG (hyaluronidase-nvhy; nivolumab) — BLA761381/5, Nov 24, 2025. Applicant at approval: Bristol-Myers Squibb Company. source ↗
- FDA New indication / efficacy supplement: OPDIVO QVANTIG (hyaluronidase-nvhy; nivolumab) — BLA761381/2, Oct 27, 2025. Applicant at approval: Bristol-Myers Squibb Company. source ↗
- FDA New indication / efficacy supplement: OPDIVO QVANTIG (hyaluronidase-nvhy; nivolumab) — BLA761381/1, Oct 27, 2025. Applicant at approval: Bristol-Myers Squibb Company. source ↗
- FDA New indication / efficacy supplement: OPDIVO (nivolumab) — BLA125554/133, May 23, 2025. Applicant at approval: Bristol-Myers Squibb Company. source ↗
- FDA New indication / efficacy supplement: CAMZYOS (mavacamten) — NDA214998/10, Apr 17, 2025. Applicant at approval: Bristol-Myers Squibb Company. source ↗
- FDA New indication / efficacy supplement: ELIQUIS (apixaban) — NDA202155/40, Apr 17, 2025. Applicant at approval: Bristol-Myers Squibb Company. source ↗
- FDA New indication / efficacy supplement: ELIQUIS (apixaban) — NDA202155/39, Apr 17, 2025. Applicant at approval: Bristol-Myers Squibb Company. source ↗
- FDA New indication / efficacy supplement: YERVOY (ipilimumab) — BLA125377/133, Apr 11, 2025. Applicant at approval: Bristol-Myers Squibb Company. source ↗
- FDA New indication / efficacy supplement: OPDIVO (nivolumab) — BLA125554/129, Apr 11, 2025. Applicant at approval: Bristol-Myers Squibb Company. source ↗
- FDA New indication / efficacy supplement: OPDIVO (nivolumab) — BLA125554/132, Apr 8, 2025. Applicant at approval: Bristol-Myers Squibb Company. source ↗
- FDA New indication / efficacy supplement: YERVOY (ipilimumab) — BLA125377/135, Apr 8, 2025. Applicant at approval: Bristol-Myers Squibb Company. source ↗
- FDA New indication / efficacy supplement: YERVOY (ipilimumab) — BLA125377/132, Jan 28, 2025. Applicant at approval: Bristol-Myers Squibb Company. source ↗
- FDA Original approval: OPDIVO QVANTIG (hyaluronidase-nvhy; nivolumab) — BLA761429, Dec 27, 2024. Applicant at approval: Bristol Myers Squibb, Company. source ↗
- FDA Original approval: OPDIVO QVANTIG (hyaluronidase-nvhy; nivolumab) — BLA761381, Dec 27, 2024. Applicant at approval: Bristol Myers Squibb, Company. Accelerated approval. source ↗
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