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Data updated: Jun 28, 2026

AKESO BIOPHARMA

Biotech
OncologyGastroenterologyImmunology Execution: Needs Improvement

AKESO BIOPHARMA is a biotechnology company focused on Oncology, Gastroenterology, Immunology.

2025
Since
1
Drugs
-
Trials
1
New Drugs (2yr)

FDA Novel Drug Designations

(2025)
1 Novel 1 Orphan 1 Breakthrough 1 Fast Track
See 1 novel approval →
2025 PENPULIMAB-KCQX Orphan · Breakthrough · Fast Track

AKESO BIOPHARMA at a Glance

  • Fast trial execution (28 months median completion)

AKESO BIOPHARMA's Key Drugs

AKESO BIOPHARMA's key approved drugs from the last 15 years (excludes generics, biosimilars and IV formulations).

No active drugs

AKESO BIOPHARMA's Recent FDA Approvals

AKESO BIOPHARMA secured 1 new FDA approval for novel drugs (NDA/BLA) in the last two years.

AKESO BIOPHARMA's Therapeutic Areas

AKESO BIOPHARMA'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 74%
1 drugs Phase 3: 23 Phase 2: 30 Phase 1: 47
Gastroenterology 8%
0 drugs Phase 3: 4 Phase 2: 1 Phase 1: 5
Immunology 8%
0 drugs Phase 3: 3 Phase 2: 3 Phase 1: 3
Dermatology 7%
0 drugs Phase 3: 2 Phase 2: 5 Phase 1: 1
Cardiovascular 3%
0 drugs Phase 2: 4 Phase 1: 1

AKESO BIOPHARMA's Top Competitors

AKESO BIOPHARMA's closest competitors by therapeutic-area and drug-target overlap include BAUSCH, Pfizer, and Takeda. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

AKESO BIOPHARMA Pipeline Snapshot

AKESO BIOPHARMA has 132 active clinical programs from ClinicalTrials.gov — 32 Phase 3, 43 Phase 2 and 57 Phase 1.

32
Phase 3
43
Phase 2
57
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q4 2026
Cadonilimab (AK104)
NSCLC (Non-small Cell Lung Cancer)
Estimated · stale NCT06617416
Q4 2026
AK112, Gemcitabine, Cisplatin
Biliary Tract Cancer
Estimated · fresh NCT06591520
Q4 2026
cadonilimab
Gastric and Gastroesophageal Junction Adenocarcinoma
Estimated · stale NCT06341335
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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

  • Top drug revenue breakdown
  • Drug-level revenue analysis

Trial Catalysts

  • Oncology pipeline focus
  • 8 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: 9/33 completed
  • Speed: 28 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