Company profile

BRISTOL MYERS SQUIBB CO

NYSE:BMYBiotechnology: Pharmaceutical Preparations

Drug pipeline (334)

AssetStageRevenueTrialsStatus
ELIQUISapproved$4.5BQ2 202629approved
OPDIVOapproved$2.7BQ2 2026222approved
OPDIVOapproved$2.7BQ2 2026222approved
ORENCIAapproved$1.0BQ2 202653approved
ORENCIAapproved$1.0BQ2 202653approved

Revenue is the latest quarter the company reported for that product, from SEC filings; a fourth quarter is the year less nine months when no filing states one. Trial counts are of the product's ingredients, deduplicated by trial, so products sharing an ingredient share trials.

Clinical trials (1727)

NCT IDPhaseStatusStartCompletionSponsor nameTitle
NCT01733875phase1completed2012-11-012013-10-09Celgene2-part Study to Assess Safety, Pharmacokinetics & Pharmacodynamics of CC-220 & Effect of Food on CC-220 in Healthy Subjects
NCT02034773phase1completed2013-05-012013-12-01Celgene Corporation3-part Study to Evaluate Safety, Tolerability, Pharmacokinetics & Pharmacodynamics of Multiple Doses of CC-220 and Relative Bioavailability of a Formulated CC-220 Capsule
NCT02323594phase1completed2014-12-012015-02-01Bristol-Myers SquibbA Bioequivalence Study of Daclatasvir Tablets and Bioavailability Studies of Daclatasvir and Asunaprevir
NCT02156076phase2terminated2014-07-252016-06-01Bristol-Myers SquibbA Blinded Study to Evaluate Effect on Atrial Fibrillation Burden in Patients With Paroxysmal Atrial Fibrillation
NCT04151563phase1_2withdrawn2021-04-152023-12-17Bristol-Myers SquibbA Clinical Study Evaluating Nivolumab-containing Treatments in Patients With Advanced Non-small Cell Lung Cancer After Failing Previous PD-1/(L)1 Therapy and Chemotherapy

FDA applications (248)

ApplicationApprovedTypeApplicantProducts
NDA 2210752026-08-13NDABRISTOL MYERS SQUIBB CO
NDA 2200732025-04-17NDABRISTOL MYERS SQUIBB CO
BLA 7613812024-12-27BLABRISTOL-MYERS SQUIBB COMPANY
NDA 2161582024-09-26NDABRISTOL-MYERS SQUIBB CO
NDA 2182132023-11-15NDABRISTOL MYERS SQUIBB CO