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Data updated: Jun 28, 2026

AVEO PHARMS

Pharma
Oncology Execution: Good

AVEO PHARMS is a pharmaceutical company focused on Oncology. Key products include FOTIVDA.

2021
Since
1
Drugs
-
Trials
0
New Drugs (2yr)
Modality:
1 Small Molecules

FDA Novel Drug Designations

(2021)
1 Novel
See 1 novel approval →
2021 FOTIVDA (TIVOZANIB HYDROCHLORIDE)

AVEO PHARMS at a Glance

  • Fast trial execution (27 months median completion)

AVEO PHARMS's Key Drugs

AVEO PHARMS's core commercial portfolio centers on FOTIVDA, spanning Oncology — its most strategically important drugs approved in the last 15 years.

AVEO PHARMS's Recent FDA Approvals

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

No recent approvals

AVEO PHARMS's Therapeutic Areas

AVEO PHARMS's approved drugs and pipeline span 1 therapeutic area, led by Oncology, across 0 biologic and 1 small-molecule drug. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Oncology 100%
1 drugs

AVEO PHARMS's Top Competitors

AVEO PHARMS's closest competitors by therapeutic-area and drug-target overlap include Pfizer, Novartis, and Merck. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

AVEO PHARMS Pipeline Snapshot

Active clinical trials for AVEO PHARMS across all therapeutic areas, from ClinicalTrials.gov.

No active pipeline data available

Phase 3 Readout Calendar Pro

1 Phase 3 trial with confidence-graded primary completion dates.

Full calendar →
Q3 2027
Ficlatuzumab
Metastatic Head-and-neck Squamous-cell Carcinoma
Estimated · fresh NCT06064877

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

  • FOTIVDA leads revenue
  • Drug-level revenue analysis

Trial Catalysts

  • Oncology pipeline focus
  • 1 Phase 3 readout 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: 3/5 completed
  • Speed: 27 months avg
Unlock Full Intelligence

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