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Data updated: Jun 28, 2026

CSL Behring

Biotech

CSL Behring is a biotechnology company focused on Immunology, Neurology, Respiratory. Key products include Flucelvax, Flucelvax Quadrivalent.

1976
Since
27
Drugs
-
Trials
1
New Drugs (2yr)
Modality:
14 Biologics

FDA Novel Drug Designations

(2025)
1 Novel 1 First-in-Class 1 Orphan 1 Fast Track
See 1 novel approval →
2025 ANDEMBRY (GARADACIMAB-GXII) First-in-Class · Orphan · Fast Track

CSL Behring at a Glance

  • Growing R&D activity with 15 trials in last 2 years
  • Fast trial execution (27 months median completion)

CSL Behring's Key Drugs

CSL Behring's core commercial portfolio centers on ANDEMBRY, Corifact, Flucelvax, Flucelvax Quadrivalent, spanning Immunology and Neurology — its most strategically important drugs approved in the last 15 years.

CSL Behring's Recent FDA Approvals

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

CSL Behring's Therapeutic Areas

CSL Behring's approved drugs and pipeline span 5 therapeutic areas, led by Immunology and Neurology, across 14 biologic and 0 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Immunology 36%
0 drugs Phase 3: 1 Phase 2: 5 Phase 1: 3
Neurology 28%
0 drugs Phase 3: 3 Phase 1: 1
Respiratory 23%
0 drugs Phase 3: 1 Phase 2: 2 Phase 1: 3
Infectious Disease 11%
0 drugs Phase 2: 2 Phase 1: 1
Cardiovascular 2%
0 drugs Phase 1: 1

CSL Behring Pipeline Snapshot

CSL Behring has 23 active clinical programs from ClinicalTrials.gov — 5 Phase 3, 9 Phase 2 and 9 Phase 1.

5
Phase 3
9
Phase 2
9
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q4 2026
Recombinant single-chain factor VIII (rVIII-SingleChain)
Congenital Hemophilia A
Estimated · fresh NCT06738485
Q4 2026
BE1116
Complex Cardiovascular Surgery With Cardiopulmonary Bypass
Estimated · fresh NCT07094087
Q4 2026
aQIV or aTIV
Influenza, Human
Estimated · fresh NCT06087640
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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

  • ANDEMBRY leads revenue
  • 5 key drugs tracked

Trial Catalysts

  • Immunology pipeline focus
  • 8 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: 29/42 completed
  • Speed: 27 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