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Data updated: Jun 28, 2026

Bristol-Myers Squibb

BMY Big Pharma

Oncology and immunology leader with Opdivo, Revlimid, and Eliquis franchises. Known for strategic acquisitions including Celgene and recent cell therapy deals.

$48.3B
Revenue (2024)
$95.0B
Market Cap
-
Trials
6
New Drugs (2yr)
Modality:
23 Small Molecules 8 Biologics

FDA Novel Drug Designations

(2017-2024)
10 Novel 6 First-in-Class 7 Orphan 2 Breakthrough 1 Accelerated 5 Priority Review 4 Fast Track
See 10 novel approvals →
2024 COBENFY (TROSPIUM CHLORIDE) First-in-Class
2023 AUGTYRO (REPOTRECTINIB) Orphan · Priority Review
2022 SOTYKTU (DEUCRAVACITINIB) First-in-Class
2022 CAMZYOS (MAVACAMTEN) First-in-Class · Orphan · Breakthrough
2022 KRAZATI (ADAGRASIB) Orphan · Breakthrough · Accelerated · Fast Track
2022 OPDUALAG (NIVOLUMAB) First-in-Class · Orphan · Priority Review · Fast Track
2020 ZEPOSIA (OZANIMOD HYDROCHLORIDE)
2019 REBLOZYL (LUSPATERCEPT-AAMT) First-in-Class · Orphan · Priority Review · Fast Track
2019 INREBIC (FEDRATINIB HYDROCHLORIDE) Orphan · Priority Review
2017 IDHIFA (ENASIDENIB MESYLATE) First-in-Class · Orphan · Priority Review · Fast Track

Bristol-Myers Squibb at a Glance

  • Leading 13 drug targets across portfolio
  • Fast trial execution (20 months median completion)

Upcoming FDA Decisions

Full Calendar →
Aug 17, 2026 — Iberdomide + daratumumab/dexamethasone
Sep 30, 2026 — Camzyos (mavacamten)

Bristol-Myers Squibb's Key Drugs

Bristol-Myers Squibb's core commercial portfolio centers on OPDIVO, ELIQUIS, YERVOY, spanning Oncology and Immunology — its most strategically important drugs approved in the last 15 years.

Bristol-Myers Squibb's Therapeutic Areas

Bristol-Myers Squibb's approved drugs and pipeline span 5 therapeutic areas, led by Oncology and Immunology, across 8 biologic and 23 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Oncology 61%
17 drugs Phase 3: 124 Phase 2: 153 Phase 1: 282
Immunology 15%
4 drugs Phase 3: 38 Phase 2: 34 Phase 1: 48
Infectious Disease 14%
3 drugs Phase 3: 35 Phase 2: 33 Phase 1: 41
Gastroenterology 5%
4 drugs Phase 3: 5 Phase 2: 16 Phase 1: 25
Neurology 5%
1 drugs Phase 3: 16 Phase 2: 6 Phase 1: 15

Bristol-Myers Squibb Pipeline Snapshot

Bristol-Myers Squibb has 871 active clinical programs from ClinicalTrials.gov — 218 Phase 3, 242 Phase 2 and 411 Phase 1.

218
Phase 3
242
Phase 2
411
Phase 1

Phase 3 Readout Calendar Pro

8 Phase 3 trials with confidence-graded primary completion dates.

Full calendar →
Q3 2026
Mezigdomide
Relapsed or Refractory Multiple Myeloma
Estimated · fresh NCT05552976
Q3 2026
BMS-986165
Psoriasis
Estimated · aging NCT04036435
Q4 2026
BMS-986278
Idiopathic Pulmonary Fibrosis
Estimated · fresh NCT06003426
Unlock 5 more readouts with confidence-graded estimates
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Anchored on CT.gov primary completion date. Topline announcements typically precede this by 3–9 months. Confidence labels combine date type (ACTUAL/ESTIMATED) with last-update freshness.

Pro Intelligence Preview

Deep insights for investors and analysts

Revenue Insights

  • OPDIVO leads revenue
  • 5 key drugs tracked
View revenue breakdown →

Trial Catalysts

  • Oncology pipeline focus
  • 8 Phase 3 readouts tracked
View readout calendar →

Patent Risk

  • Patent expiration timeline
  • Revenue at risk analysis
View patent timeline →

Compare Companies

  • Side-by-side pipeline analysis
  • Revenue & market share comparison
Compare with competitor →

Execution Intelligence

  • Phase 3: 113/184 completed
  • Speed: 20 months avg
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Revenue forecasts • Trial milestones • Patent risk modeling

How We Calculate These Metrics

Execution Quality Score

Measures trial completion rates weighted by phase importance. Phase 3 trials count 4x more than Phase 1 because late-stage completion is harder and more valuable.

What counts as "completed": A trial that reached its planned endpoint and reported results. Trials that were terminated early, withdrawn, or suspended are not counted as completed—these often indicate safety issues, lack of efficacy, or strategic pivots.

  • Excellent (80%+): Top-tier execution, most trials reach planned endpoints
  • Good (60-79%): Strong execution with occasional early terminations
  • Fair (40-59%): Average execution, notable rate of terminated/withdrawn trials
  • Needs Improvement (under 40%): High termination rates, execution challenges