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Data updated: May 24, 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)
Novel Drugs (2025):
1 Novel Approvals 1 Orphan Drug 1 Breakthrough

AKESO BIOPHARMA at a Glance

  • Fast trial execution (28 months median completion)

Key Drugs

Top revenue-generating and strategically important drugs approved in the last 15 years. These represent the company's core commercial portfolio.

No active drugs

Recent FDA Approvals

New drug approvals (NDA/BLA) in the last 2 years. Shows novel drugs only, excluding generics and label supplements.

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.

Oncology 74%
1 drugs Phase 3: 23 Phase 2: 29 Phase 1: 45
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

Pipeline Snapshot

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

32
Phase 3
42
Phase 2
55
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q2 2026
AK104
Locally Advanced Cervical Carcinoma
Estimated · stale NCT05235516
Q4 2026
Cadonilimab (AK104)
NSCLC (Non-small Cell Lung Cancer)
Estimated · stale NCT06617416
Q4 2026
AK112, Gemcitabine, Cisplatin
Biliary Tract Cancer
Estimated · fresh NCT06591520
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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