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Data updated: Jun 28, 2026

BIO-THERA SOLUTIONS LTD

Biotech

BIO-THERA SOLUTIONS LTD is a biotechnology company focused on Oncology, Immunology, Ophthalmology.

2023
Since
2
Drugs
-
Trials
1
New Drugs (2yr)

BIO-THERA SOLUTIONS LTD at a Glance

  • Fast trial execution (25 months median completion)

BIO-THERA SOLUTIONS LTD's Key Drugs

BIO-THERA SOLUTIONS LTD's key approved drugs from the last 15 years (excludes generics, biosimilars and IV formulations).

No active drugs

BIO-THERA SOLUTIONS LTD's Recent FDA Approvals

BIO-THERA SOLUTIONS LTD secured 1 new FDA approval for novel drugs (NDA/BLA) in the last two years.

BIO-THERA SOLUTIONS LTD's Therapeutic Areas

BIO-THERA SOLUTIONS LTD's approved drugs and pipeline span 5 therapeutic areas, led by Oncology and Immunology. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Oncology 45%
1 drugs Phase 3: 2 Phase 2: 2 Phase 1: 19
Immunology 33%
1 drugs Phase 3: 4 Phase 1: 5
Ophthalmology 14%
0 drugs Phase 3: 2 Phase 2: 1 Phase 1: 2
Gastroenterology 7%
1 drugs
Dermatology 1%
0 drugs Phase 1: 1

BIO-THERA SOLUTIONS LTD's Top Competitors

BIO-THERA SOLUTIONS LTD's closest competitors by therapeutic-area and drug-target overlap include BAUSCH, Pfizer, and Novartis. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

BIO-THERA SOLUTIONS LTD Pipeline Snapshot

BIO-THERA SOLUTIONS LTD has 38 active clinical programs from ClinicalTrials.gov — 8 Phase 3, 3 Phase 2 and 27 Phase 1.

8
Phase 3
3
Phase 2
27
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q3 2026
Recombinant humanized anti-PD-1 monoclonal antibody injection
Cervical Cancer
Estimated · stale NCT06123884
Q2 2027
BAT5906 injection
Diabetic Macular Edema (DME)
Estimated · fresh NCT07515079
Q4 2030
BAT4406F
Minimal Change Disease (MCD)
Estimated · fresh NCT07499700

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
  • 3 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: 7/9 completed
  • Speed: 25 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