TheraRadar
← Back
Data updated: Jun 28, 2026

USWM

Specialty
OncologyGastroenterology Execution: Needs Improvement

USWM is a specialty pharmaceutical company focused on Oncology, Gastroenterology. Key products include IWILFIN.

1979
Since
4
Drugs
-
Trials
0
New Drugs (2yr)
Modality:
1 Small Molecules

USWM's Key Drugs

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

USWM's Recent FDA Approvals

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

No recent approvals

USWM's Therapeutic Areas

USWM's approved drugs and pipeline span 2 therapeutic areas, led by Oncology and Gastroenterology, across 0 biologic and 1 small-molecule drug. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Oncology 88%
0 drugs Phase 2: 5 Phase 1: 4
Gastroenterology 13%
0 drugs Phase 1: 2

USWM's Top Competitors

USWM'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.

USWM Pipeline Snapshot

USWM has 11 active clinical programs from ClinicalTrials.gov — 0 Phase 3, 5 Phase 2 and 6 Phase 1.

0
Phase 3
5
Phase 2
6
Phase 1

Pro Intelligence Preview

Deep insights for investors and analysts

Revenue Insights

  • IWILFIN leads revenue
  • Drug-level revenue analysis

Trial Catalysts

  • Oncology 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: 0/0 completed
  • Speed: N/A 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 Trials that were terminated early, withdrawn, or suspended are not counted as completed—these often indicate safety issues, lack of efficacy, or strategic pivots.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