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Data updated: May 24, 2026

Regeneron

REGN Biotech

Biotechnology leader known for Eylea (ophthalmology) and Dupixent (immunology, co-developed with Sanofi). Strong antibody discovery platform.

$14.9B
Revenue (2024)
$85.0B
Market Cap
-
Trials
0
New Drugs (2yr)
Modality:
5 Biologics
Novel Drugs (2017-2023):
5 Novel Approvals 4 First-in-Class 3 Orphan Drug 4 Breakthrough

Regeneron at a Glance

  • Growing R&D activity with 71 trials in last 2 years
  • Fast trial execution (19 months median completion)

Upcoming FDA Decisions

Full Calendar →
Aug 19, 2026 — Garetosmab

Recent FDA Approvals

New drug approvals (NDA/BLA) in the last 2 years. Shows novel drugs only, excluding generics and label supplements.

No recent approvals

Therapeutic Areas

Disease areas where this company has approved drugs and active pipeline. Weighted by commercial stage: approved drugs count most, followed by late-stage trials.

Oncology 41%
1 drugs Phase 3: 18 Phase 2: 26 Phase 1: 35
Cardiovascular 20%
2 drugs Phase 3: 11 Phase 2: 10 Phase 1: 3
Dermatology 18%
1 drugs Phase 3: 10 Phase 2: 9 Phase 1: 8
Ophthalmology 14%
2 drugs Phase 3: 7 Phase 2: 6 Phase 1: 4
Immunology 8%
0 drugs Phase 3: 4 Phase 2: 4 Phase 1: 7

Pipeline Snapshot

Active clinical trials across all therapeutic areas. Data from ClinicalTrials.gov.

50
Phase 3
55
Phase 2
57
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q3 2026
mibavademab
Generalized Lipodystrophy
Estimated · fresh NCT06548100
Q4 2026
Dupilumab
Atopic Dermatitis
Estimated · aging NCT02612454
Q1 2027
Ravulizumab
Paroxysmal Nocturnal Hemoglobinuria
Estimated · fresh NCT05133531
Unlock 5 more readouts with confidence-graded estimates
Upgrade to Pro

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

  • DUPIXENT 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: 43/85 completed
  • Speed: 19 months avg
Unlock Full Intelligence

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