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Data updated: Jun 28, 2026

Octapharma

Biotech

Octapharma is a biotechnology company focused on Immunology, Neurology, Cardiovascular. Key products include Octaplas.

2004
Since
8
Drugs
-
Trials
0
New Drugs (2yr)
Modality:
5 Biologics

Octapharma at a Glance

  • Fast trial execution (29 months median completion)

Octapharma's Key Drugs

Octapharma's core commercial portfolio centers on Octaplas, Nuwiq, Panzyga, spanning Immunology and Neurology — its most strategically important drugs approved in the last 15 years.

Octapharma's Recent FDA Approvals

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

No recent approvals

Octapharma's Therapeutic Areas

Octapharma's approved drugs and pipeline span 5 therapeutic areas, led by Immunology and Neurology, across 5 biologic and 0 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Immunology 42%
0 drugs Phase 3: 4 Phase 1: 2
Neurology 28%
0 drugs Phase 3: 2 Phase 2: 2
Cardiovascular 12%
0 drugs Phase 3: 1 Phase 1: 1
Infectious Disease 9%
0 drugs Phase 3: 1
Oncology 9%
0 drugs Phase 3: 1

Octapharma Pipeline Snapshot

Octapharma has 14 active clinical programs from ClinicalTrials.gov — 9 Phase 3, 2 Phase 2 and 3 Phase 1.

9
Phase 3
2
Phase 2
3
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q4 2026
OCTA-C1-INH
Acute Hereditary Angio Edema
Estimated · aging NCT06361537
Q1 2028
Human plasma derived antithrombin
Acquired Antithrombin Deficiency
Estimated · fresh NCT06096116
Q4 2029
Panzyga, 10% Intravenous Solution
Hypogammaglobulinemia
Estimated · aging NCT07220915
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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

  • Octaplas leads revenue
  • 5 key drugs tracked

Trial Catalysts

  • Immunology pipeline focus
  • 4 Phase 3 readouts 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: 28/37 completed
  • Speed: 29 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