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Data updated: Jul 17, 2026

Kedrion Biopharma

Biotech
ImmunologyNeurology Execution: Needs Improvement

Kedrion Biopharma is a biotechnology company focused on Immunology, Neurology. Key products include QIVIGY.

1998
Since
4
Drugs
-
Trials
1
New Drugs (2yr)
Modality:
2 Biologics

Kedrion Biopharma at a Glance

  • Fast trial execution (21 months median completion)

Kedrion Biopharma's Key Drugs

Kedrion Biopharma's core commercial portfolio centers on Kedbumin, Ryplazim, QIVIGY, spanning Immunology and Neurology — its most strategically important drugs approved in the last 15 years.

Kedrion Biopharma's Recent FDA Approvals

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

Kedrion Biopharma's Therapeutic Areas

Kedrion Biopharma's approved drugs and pipeline span 2 therapeutic areas, led by Immunology and Neurology, across 2 biologic and 0 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Immunology 75%
0 drugs Phase 3: 3
Neurology 25%
0 drugs Phase 3: 1

Kedrion Biopharma's Top Competitors

Kedrion Biopharma'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.

Kedrion Biopharma Pipeline Snapshot

Kedrion Biopharma has 4 active clinical programs from ClinicalTrials.gov — 4 Phase 3, 0 Phase 2 and 0 Phase 1.

4
Phase 3
0
Phase 2
0
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q3 2026
Kedrion IVIG 10%
Chronic Primary Immune Thrombocytopenia (ITP)
Estimated · fresh NCT07059000
Q4 2027
Immune globulin (human) 10% solution for intravenous administration
Chronic Inflammatory Demyelinating Polyneuropathy
Estimated · fresh NCT06752356

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

  • Kedbumin leads revenue
  • 3 key drugs tracked

Trial Catalysts

  • Immunology pipeline focus
  • 2 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: 2/7 completed
  • Speed: 21 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