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Data updated: Jun 28, 2026

MEDA PHARMS

Specialty
ImmunologyGastroenterology Execution: Excellent

MEDA PHARMS is a specialty pharmaceutical company focused on Immunology, Gastroenterology.

1960
Since
7
Drugs
-
Trials
0
New Drugs (2yr)

MEDA PHARMS at a Glance

  • Strong track record with 100% execution quality across 11 trials
  • Fast trial execution (10 months median completion)

MEDA PHARMS's Key Drugs

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

No active drugs

MEDA PHARMS's Recent FDA Approvals

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

No recent approvals

MEDA PHARMS's Therapeutic Areas

MEDA PHARMS's approved drugs and pipeline span 2 therapeutic areas, led by Immunology and Gastroenterology. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Immunology 50%
1 drugs
Gastroenterology 50%
1 drugs

MEDA PHARMS's Top Competitors

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

MEDA PHARMS Pipeline Snapshot

Active clinical trials for MEDA PHARMS across all therapeutic areas, from ClinicalTrials.gov.

No active pipeline data available

Pro Intelligence Preview

Deep insights for investors and analysts

Revenue Insights

  • Top drug revenue breakdown
  • Drug-level revenue analysis

Trial Catalysts

  • Immunology pipeline focus
  • Phase 3 readout tracking

Patent Risk

  • Patent expiration timeline
  • Revenue at risk analysis

Compare Companies

  • Side-by-side pipeline analysis
  • Revenue & market share comparison

Execution Intelligence

  • Phase 3: 10/10 completed
  • Speed: 10 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 Trials that were terminated early, withdrawn, or suspended are not counted as completed—these often indicate safety issues, lack of efficacy, or strategic pivots.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