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Data updated: Jun 28, 2026

GUERBET

Specialty
OncologyMetabolic Execution: Good

GUERBET is a specialty pharmaceutical company focused on Oncology, Metabolic. Key products include DOTAREM.

1954
Since
6
Drugs
-
Trials
0
New Drugs (2yr)
Modality:
3 Small Molecules

FDA Novel Drug Designations

(2022)
1 Novel 1 Priority Review
See 1 novel approval →
2022 ELUCIREM (GADOPICLENOL) Priority Review

GUERBET at a Glance

  • Fast trial execution (16 months median completion)

GUERBET's Key Drugs

GUERBET's core commercial portfolio centers on DOTAREM, ELUCIREM, spanning Oncology and Metabolic — its most strategically important drugs approved in the last 15 years.

GUERBET's Recent FDA Approvals

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

No recent approvals

GUERBET's Therapeutic Areas

GUERBET's approved drugs and pipeline span 2 therapeutic areas, led by Oncology and Metabolic, across 0 biologic and 3 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Oncology 94%
1 drugs Phase 3: 1 Phase 2: 1 Phase 1: 4
Metabolic 6%
0 drugs Phase 1: 1

GUERBET's Top Competitors

GUERBET's closest competitors by therapeutic-area and drug-target overlap include Merck, Baxter, and Johnson & Johnson. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

GUERBET Pipeline Snapshot

GUERBET has 7 active clinical programs from ClinicalTrials.gov — 1 Phase 3, 1 Phase 2 and 5 Phase 1.

1
Phase 3
1
Phase 2
5
Phase 1

Phase 3 Readout Calendar Pro

1 Phase 3 trial with confidence-graded primary completion dates.

Full calendar →
Q4 2027
gadopiclenol
Steno-occlusive Disease
Estimated · fresh NCT07348640

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

  • DOTAREM leads revenue
  • 2 key drugs tracked

Trial Catalysts

  • Oncology pipeline focus
  • 1 Phase 3 readout 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: 7/10 completed
  • Speed: 16 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