Autopsy report · NCT03329885
A Study of Experimental Medication BMS-986251, Taken by Mouth, in Healthy Participants and Patients With Average to Very Serious Psoriasis
Cause of deathSafety
“Adverse change in the risk/benefit”
Life of this trial
- Ran for about 8 months before it stopped.
- 38 participants enrolled.
- Results were posted on the registry 1 year 4 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1, Phase 2
- Sponsor
- Bristol-Myers Squibb
- Sponsor type
- Industry
- Conditions
- Rheumatoid Arthritis; Psoriasis; Ankylosing Spondylitis; Inflammatory Bowel Diseases; Nonalcoholic Steatohepatitis
- Interventions
- BMS-986251; Placebo
- Participants
- 38
- Sites
- 1
- Countries
- Netherlands
Trials that died the same way
- High Flow Oxygen in Patients Undergoing Suspension Laryngoscopy Under General Anesthesia
“Risk-benefit analysis” - A Clinical Study to Test How Effective and Safe GLPG1690 is for Subjects With Idiopathic Pulmonary Fibrosis (IPF) When Used Together With Standard of Care
“The benefit-risk profile no longer supports continuing the study” - Phase I Trial of AZD1775 and Belinostat in Treating Patients With Relapsed or Refractory Myeloid Malignancies or Untreated Acute Myeloid Leukemia
“Other - Adverse Events” - Safety and Bioactivity of AXT107 in Subjects With Diabetic Macular Edema
“Adverse Events” - MB-CART20.1 Melanoma
“The risk-benefit assessment was not as expected.”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.