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Data updated: Jun 28, 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:
33 Small Molecules 18 Biologics

FDA Novel Drug Designations

(2017-2023)
5 Novel 1 First-in-Class 3 Orphan 3 Breakthrough 2 Accelerated 4 Priority Review 2 Fast Track
See 5 novel approvals →
2023 FRUZAQLA (FRUQUINTINIB) Priority Review · Fast Track
2021 LIVTENCITY (MARIBAVIR) First-in-Class · Orphan · Breakthrough · Priority Review
2021 EXKIVITY (MOBOCERTINIB SUCCINATE) Orphan · Breakthrough · Priority Review · Accelerated · Fast Track
2018 MOTEGRITY (PRUCALOPRIDE SUCCINATE)
2017 ALUNBRIG (BRIGATINIB) Orphan · Breakthrough · Priority Review · Accelerated

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)
30d
Sep 2, 2026 — Rusfertide

Takeda's Recent FDA Approvals

New NDA/BLA approvals for Takeda over the last two years — novel drugs only, excluding generics and label supplements.

No recent approvals

Takeda's Therapeutic Areas

Takeda's approved drugs and pipeline span 5 therapeutic areas, led by Immunology and Metabolic, across 18 biologic and 33 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then 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

Takeda Pipeline Snapshot

Takeda has 310 active clinical programs from ClinicalTrials.gov — 141 Phase 3, 62 Phase 2 and 107 Phase 1.

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 →
Q3 2026
Tetravalent Dengue Vaccine (TDV)
Dengue Fever
Estimated · fresh NCT07047521
Q4 2026
TAK-861
Narcolepsy Type 1 (NT1)
Estimated · fresh NCT07363720
Q4 2026
TAK-788
Advanced/Metastatic Non-Small Cell Lung Cancer (NSCLC)
Estimated · fresh NCT04129502
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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
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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