Biopharma Transcript

Bristol Myers Squibb Co BMY

NYSE · Phase 3 · oncology · biologic-other · EDGAR · Updated Oct 24, 2026

Bristol Myers Squibb Co (NYSE: BMY) is an oncology drug developer. Its lead program, Marketed portfolio (Opdivo, Eliquis, Reblozyl, Breyanzi, Camzyos, Cobenfy, others), is in Phase 3 for oncology, hematology, immunology, cardiovascular, neuroscience. Its next catalyst on record is Reblozyl: PDUFA date, sBLA for MF-associated anemia (March 11, 2027).

Upcoming catalysts

  1. March 11, 2027
    Reblozyl — PDUFA date, sBLA for MF-associated anemiaThe FDA granted a PDUFA date of March 11, 2027.
  2. May 13, 2027
    mezigdomide — PDUFA date, NDA for MeziKd in RRMMThe FDA has granted a PDUFA date of May 13, 2027 for this indication.

Next further out: Registrational programs (AR LDD, Sotyktu SLE/SjS, admilparant, milvexian, Cobenfy, arlo-cel, iberdomide, others) — Registrational study readouts (2026). 1 catalyst on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
Reblozyl sNDA/sBLA (MF-associated anemia)myelofibrosis-associated anemiaprotein/peptideApproved
Camzyos sNDA (adolescents)symptomatic obstructive HCM, ages 12-<18small moleculeApproved
iberdomiderelapsed/refractory multiple myeloma (RRMM)small moleculePhase 3
mezigdomide + carfilzomib/dexamethasone (MeziKd)RRMMsmall moleculePhase 3
milvexian (with J&J)atrial fibrillation; secondary stroke preventionsmall moleculePhase 3
admilparantIPF; progressive pulmonary fibrosissmall moleculePhase 3
Cobenfy (additional indications)Alzheimer's disease psychosis; bipolar-Ismall moleculePhase 3
arlo-cel4L+ multiple myelomacell therapyPhase 3
pumitamig (BNT327, with BioNTech)NSCLC and other solid tumorsantibodyPhase 3
iza-bren (with SystImmune)TNBC, ESCC, NSCLCantibodyPhase 3
golcadomidefollicular lymphoma, LBCLsmall moleculePhase 3
RYZ101SSTR2+ GEP-NETsradiopharmaceuticalPhase 3

For subscribers

Other phase 3 oncology companies