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Data updated: May 24, 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
Novel Drugs (2025):
1 Novel Approvals 1 First-in-Class 1 Orphan Drug

CSL Behring at a Glance

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

Key Drugs

Top revenue-generating and strategically important drugs approved in the last 15 years. These represent the company's core commercial portfolio.

Recent FDA Approvals

New drug approvals (NDA/BLA) in the last 2 years. Shows novel drugs only, excluding generics and label supplements.

Therapeutic Areas

Disease areas where this company has approved drugs and active pipeline. Weighted by commercial stage: approved drugs count most, followed by 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

Pipeline Snapshot

Active clinical trials across all therapeutic areas. Data from ClinicalTrials.gov.

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