TheraRadar
← Back
Data updated: Jun 28, 2026

FERRING

Biotech
OncologyImmunologyGastroenterology Execution: Excellent

FERRING is a biotechnology company focused on Oncology, Immunology, Gastroenterology.

1974
Since
16
Drugs
-
Trials
0
New Drugs (2yr)
Modality:
2 Small Molecules 4 Biologics

FERRING at a Glance

  • Strong track record with 84% execution quality across 129 trials
  • Fast trial execution (18 months median completion)

FERRING's Key Drugs

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

No active drugs

FERRING's Recent FDA Approvals

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

No recent approvals

FERRING's Therapeutic Areas

FERRING's approved drugs and pipeline span 5 therapeutic areas, led by Oncology and Immunology, across 4 biologic and 2 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Oncology 58%
1 drugs Phase 3: 19 Phase 2: 2 Phase 1: 4
Immunology 22%
0 drugs Phase 3: 8 Phase 1: 2
Gastroenterology 14%
0 drugs Phase 3: 5 Phase 1: 2
Infectious Disease 3%
0 drugs Phase 3: 1
Metabolic 3%
0 drugs Phase 3: 1

FERRING Pipeline Snapshot

FERRING has 44 active clinical programs from ClinicalTrials.gov — 34 Phase 3, 2 Phase 2 and 8 Phase 1.

34
Phase 3
2
Phase 2
8
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q2 2028
Nadofaragene Firadenovec
Intermediate Risk Non-Muscle Invasive Bladder Cancer
Estimated · fresh NCT06510374
Q2 2028
Nadofaragene Firadenovec
Non-muscle Invasive Bladder Cancer With Carcinoma in Situ
Estimated · fresh NCT06545955
Q4 2029
FE 999326
Bladder Cancer
Estimated · aging NCT05704244

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

  • Top drug revenue breakdown
  • Drug-level revenue analysis
View revenue breakdown →

Trial Catalysts

  • Oncology pipeline focus
  • 3 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
Compare with competitor →

Execution Intelligence

  • Phase 3: 62/72 completed
  • Speed: 18 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