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Data updated: Jun 28, 2026

HALEON US HOLDINGS

Specialty
Gastroenterology Execution: Excellent

HALEON US HOLDINGS is a specialty pharmaceutical company focused on Gastroenterology. Key products include ADVIL ALLERGY AND CONGESTION RELIEF.

1984
Since
28
Drugs
-
Trials
0
New Drugs (2yr)
Modality:
24 Small Molecules

HALEON US HOLDINGS at a Glance

  • Strong track record with 85% execution quality across 17 trials
  • Fast trial execution (2 months median completion)

HALEON US HOLDINGS's Key Drugs

HALEON US HOLDINGS's core commercial portfolio centers on ADVIL DUAL ACTION WITH ACETAMINOPHEN, FLONASE ALLERGY RELIEF, ADVIL ALLERGY AND CONGESTION RELIEF, spanning Gastroenterology — its most strategically important drugs approved in the last 15 years.

HALEON US HOLDINGS's Recent FDA Approvals

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

No recent approvals

HALEON US HOLDINGS's Therapeutic Areas

HALEON US HOLDINGS's approved drugs and pipeline span 1 therapeutic area, led by Gastroenterology, across 0 biologic and 24 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Gastroenterology 100%
0 drugs Phase 1: 1

HALEON US HOLDINGS's Top Competitors

HALEON US HOLDINGS'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.

HALEON US HOLDINGS Pipeline Snapshot

HALEON US HOLDINGS has 1 active clinical program from ClinicalTrials.gov — 0 Phase 3, 0 Phase 2 and 1 Phase 1.

0
Phase 3
0
Phase 2
1
Phase 1

Pro Intelligence Preview

Deep insights for investors and analysts

Revenue Insights

  • ADVIL DUAL ACTION WITH ACETAMINOPHEN leads revenue
  • 4 key drugs tracked

Trial Catalysts

  • Gastroenterology 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: 2/3 completed
  • Speed: 2 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