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Data updated: Jun 28, 2026

UCB INC

Specialty
NeurologyImmunology Execution: Fair

UCB INC is a specialty pharmaceutical company focused on Neurology, Immunology. Key products include FINTEPLA.

1955
Since
34
Drugs
-
Trials
1
New Drugs (2yr)
Modality:
10 Small Molecules 1 Biologics

FDA Novel Drug Designations

(2016-2025)
5 Novel 1 First-in-Class 3 Orphan 1 Breakthrough 3 Priority Review
See 5 novel approvals →
2025 KYGEVVI (DOXECITINE) First-in-Class · Orphan · Breakthrough · Priority Review
2023 RYSTIGGO (ROZANOLIXIZUMAB-NOLI) Orphan · Priority Review
2023 ZILBRYSQ (ZILUCOPLAN SODIUM) Orphan
2023 BIMZELX (BIMEKIZUMAB-BKZX)
2016 BRIVIACT (BRIVARACETAM) Priority Review

UCB INC at a Glance

  • Growing R&D activity with 30 trials in last 2 years
  • Fast trial execution (24 months median completion)

UCB INC's Key Drugs

UCB INC's core commercial portfolio centers on BIMZELX, FINTEPLA, NAYZILAM, spanning Neurology and Immunology — its most strategically important drugs approved in the last 15 years.

UCB INC's Recent FDA Approvals

UCB INC secured 1 new FDA approval for novel drugs (NDA/BLA) in the last two years.

UCB INC's Therapeutic Areas

UCB INC's approved drugs and pipeline span 2 therapeutic areas, led by Neurology and Immunology, across 1 biologic and 10 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Neurology 78%
7 drugs
Immunology 22%
2 drugs

UCB INC's Top Competitors

UCB INC's closest competitors by therapeutic-area and drug-target overlap include Pfizer, AbbVie, and Eli Lilly. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

UCB INC Pipeline Snapshot

Active clinical trials for UCB INC across all therapeutic areas, from ClinicalTrials.gov.

No active pipeline data available

Phase 3 Readout Calendar Pro

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

Full calendar →
Q3 2026
fenfluramine
Dravet Syndrome
Estimated · fresh NCT06118255
Q3 2028
fenfluramine hydrochloride
Rett Syndrome
Estimated · fresh NCT07503444

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

  • BIMZELX leads revenue
  • 5 key drugs tracked
View revenue breakdown →

Trial Catalysts

  • Neurology pipeline focus
  • 2 Phase 3 readouts tracked
View readout calendar →

Patent Risk

  • Patent expiration timeline
  • Revenue at risk analysis
View patent timeline →

Compare Companies

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

  • Phase 3: 27/58 completed
  • Speed: 24 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