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Data updated: Jun 28, 2026

BEIGENE

Biotech

BEIGENE is a biotechnology company focused on Oncology, Gastroenterology, Immunology.

2024
Since
1
Drugs
-
Trials
2
New Drugs (2yr)

FDA Novel Drug Designations

(2024)
1 Novel 1 Orphan
See 1 novel approval →
2024 TEVIMBRA (TISLELIZUMAB-JSGR) Orphan

BEIGENE's Key Drugs

BEIGENE's core commercial portfolio centers on TEVIMBRA, spanning Oncology and Gastroenterology — its most strategically important drugs approved in the last 15 years.

BEIGENE's Recent FDA Approvals

BEIGENE secured 2 new FDA approvals for novel drugs (NDA/BLA) in the last two years.

BEIGENE's Therapeutic Areas

BEIGENE's approved drugs and pipeline span 5 therapeutic areas, led by Oncology and Gastroenterology. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Oncology 88%
1 drugs Phase 3: 20 Phase 2: 36 Phase 1: 39
Gastroenterology 8%
1 drugs Phase 3: 1 Phase 2: 2 Phase 1: 4
Immunology 2%
0 drugs Phase 2: 2 Phase 1: 1
Respiratory 1%
0 drugs Phase 2: 1
Dermatology 0%
0 drugs Phase 1: 1

BEIGENE's Top Competitors

BEIGENE's closest competitors by therapeutic-area and drug-target overlap include Pfizer, Novartis, and PF PRISM CV. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

BEIGENE Pipeline Snapshot

BEIGENE has 107 active clinical programs from ClinicalTrials.gov — 21 Phase 3, 41 Phase 2 and 45 Phase 1.

21
Phase 3
41
Phase 2
45
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q2 2027
Tislelizumab
Urothelial Carcinoma
Estimated · fresh NCT03967977
Q4 2027
Zanubrutinib
B-cell Malignancies
Estimated · aging NCT04170283
Q4 2025
Pamiparib capsule
Ovarian Cancer
Completed · awaiting NCT03519230

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

  • TEVIMBRA leads revenue
  • Drug-level revenue analysis

Trial Catalysts

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

Patent Risk

  • Patent expiration timeline
  • Revenue at risk analysis

Compare Companies

  • Side-by-side pipeline analysis
  • Revenue & market share comparison

Execution Intelligence

  • Phase 3: 12/24 completed
  • Speed: 39 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