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Data updated: May 24, 2026

Takeda

TAK Big Pharma

Takeda is a major pharmaceutical company focused on Immunology, Metabolic, Gastroenterology. Key products include ENTYVIO.

1945
Since
86
Drugs
-
Trials
0
New Drugs (2yr)
Modality:
34 Small Molecules 18 Biologics
Novel Drugs (2017-2023):
5 Novel Approvals 1 First-in-Class 3 Orphan Drug 3 Breakthrough

Takeda at a Glance

  • Leading 6 drug targets across portfolio
  • Fast trial execution (17 months median completion)

Upcoming FDA Decisions

Full Calendar →
Aug 10, 2026 — Oveporexton (TAK-861)
Sep 2, 2026 — Rusfertide

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.

Immunology 30%
3 drugs Phase 3: 47 Phase 2: 22 Phase 1: 23
Metabolic 21%
4 drugs Phase 3: 32 Phase 2: 12 Phase 1: 19
Gastroenterology 20%
4 drugs Phase 3: 29 Phase 2: 9 Phase 1: 20
Oncology 18%
6 drugs Phase 3: 15 Phase 2: 16 Phase 1: 37
Cardiovascular 11%
2 drugs Phase 3: 18 Phase 2: 3 Phase 1: 8

Pipeline Snapshot

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

141
Phase 3
62
Phase 2
107
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q2 2026
Zasocitinib
Plaque Psoriasis
Estimated · fresh NCT06973291
Q3 2026
Tetravalent Dengue Vaccine (TDV)
Dengue Fever
Estimated · fresh NCT07047521
Q4 2026
TAK-861
Narcolepsy Type 1 (NT1)
Estimated · fresh NCT07363720
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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

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

Trial Catalysts

  • Immunology 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
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Execution Intelligence

  • Phase 3: 154/220 completed
  • Speed: 17 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