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Data updated: Jun 28, 2026

TAIHO ONCOLOGY

Pharma
OncologyGastroenterology Execution: Needs Improvement

TAIHO ONCOLOGY is a pharmaceutical company focused on Oncology, Gastroenterology. Key products include INQOVI.

2015
Since
3
Drugs
-
Trials
0
New Drugs (2yr)
Modality:
2 Small Molecules

FDA Novel Drug Designations

(2020-2022)
2 Novel 2 Orphan 1 Breakthrough 1 Accelerated 2 Priority Review 1 Fast Track
See 2 novel approvals →
2022 LYTGOBI (FUTIBATINIB) Orphan · Breakthrough · Priority Review · Accelerated · Fast Track
2020 INQOVI (CEDAZURIDINE) Orphan · Priority Review

TAIHO ONCOLOGY's Key Drugs

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

TAIHO ONCOLOGY's Recent FDA Approvals

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

No recent approvals

TAIHO ONCOLOGY's Therapeutic Areas

TAIHO ONCOLOGY's approved drugs and pipeline span 2 therapeutic areas, led by Oncology and Gastroenterology, across 0 biologic and 2 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Oncology 84%
2 drugs Phase 3: 6 Phase 2: 14 Phase 1: 29
Gastroenterology 16%
1 drugs Phase 3: 2 Phase 2: 1 Phase 1: 2

TAIHO ONCOLOGY's Top Competitors

TAIHO ONCOLOGY's closest competitors by therapeutic-area and drug-target overlap include Johnson & Johnson, Bristol-Myers Squibb, and Takeda. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

TAIHO ONCOLOGY Pipeline Snapshot

TAIHO ONCOLOGY has 54 active clinical programs from ClinicalTrials.gov — 8 Phase 3, 15 Phase 2 and 31 Phase 1.

8
Phase 3
15
Phase 2
31
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q4 2026
TAS6417
Advanced or Metastatic NSCLS With Exon 20 Insertion Mutation
Estimated · fresh NCT05973773
Q2 2027
futibatinib
Advanced/Metastatic Cancer
Estimated · fresh NCT06506955
Q4 2027
Azacitidine
Myelodysplastic Syndromes
Estimated · fresh NCT04256317
Unlock 1 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

  • INQOVI leads revenue
  • 2 key drugs tracked
View revenue breakdown →

Trial Catalysts

  • Oncology pipeline focus
  • 4 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: 3/7 completed
  • Speed: 43 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