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Data updated: Jun 28, 2026

SANOFI-AVENTIS U.S. LLC

Biotech

SANOFI-AVENTIS U.S. LLC is a biotechnology company focused on Metabolic, Oncology, Cardiovascular. Key products include Toujeo.

2015
Since
3
Drugs
-
Trials
1
New Drugs (2yr)
Modality:
1 Biologics

SANOFI-AVENTIS U.S. LLC at a Glance

  • Fast trial execution (19 months median completion)

SANOFI-AVENTIS U.S. LLC's Key Drugs

SANOFI-AVENTIS U.S. LLC's core commercial portfolio centers on Toujeo, MERILOG SOLOSTAR, spanning Metabolic and Oncology — its most strategically important drugs approved in the last 15 years.

SANOFI-AVENTIS U.S. LLC's Recent FDA Approvals

SANOFI-AVENTIS U.S. LLC secured 1 new FDA approval for novel drugs (NDA/BLA) in the last two years.

SANOFI-AVENTIS U.S. LLC's Therapeutic Areas

SANOFI-AVENTIS U.S. LLC's approved drugs and pipeline span 5 therapeutic areas, led by Metabolic and Oncology, across 1 biologic and 0 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Metabolic 38%
2 drugs Phase 3: 69 Phase 2: 11 Phase 1: 99
Oncology 29%
0 drugs Phase 3: 32 Phase 2: 49 Phase 1: 88
Cardiovascular 13%
0 drugs Phase 3: 27 Phase 2: 8 Phase 1: 15
Immunology 11%
0 drugs Phase 3: 14 Phase 2: 21 Phase 1: 19
Respiratory 9%
0 drugs Phase 3: 15 Phase 2: 14 Phase 1: 9

SANOFI-AVENTIS U.S. LLC's Top Competitors

SANOFI-AVENTIS U.S. LLC's closest competitors by therapeutic-area and drug-target overlap include Novartis, AstraZeneca, and Merck. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

SANOFI-AVENTIS U.S. LLC Pipeline Snapshot

SANOFI-AVENTIS U.S. LLC has 490 active clinical programs from ClinicalTrials.gov — 157 Phase 3, 103 Phase 2 and 230 Phase 1.

157
Phase 3
103
Phase 2
230
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q3 2026
Yellow fever vaccine (live)
Yellow Fever Immunization
Estimated · fresh NCT07103148
Q4 2026
rilzabrutinib
Immune Thrombocytopenia
Estimated · aging NCT07216079
Q4 2026
PCV21
Pneumococcal Infections
Estimated · aging NCT06838000
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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

  • Toujeo leads revenue
  • 2 key drugs tracked

Trial Catalysts

  • Metabolic 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: 224/312 completed
  • Speed: 19 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