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Data updated: Jun 28, 2026

VERASTEM INC

Pharma
Oncology Execution: Needs Improvement

VERASTEM INC is a pharmaceutical company focused on Oncology. Key products include AVMAPKI FAKZYNJA CO-PACK (COPACKAGED).

2025
Since
1
Drugs
-
Trials
1
New Drugs (2yr)
Modality:
1 Small Molecules

FDA Novel Drug Designations

(2025)
1 Novel 1 First-in-Class 1 Orphan 1 Breakthrough 1 Accelerated 1 Priority Review
See 1 novel approval →
2025 AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) (AVUTOMETINIB POTASSIUM) First-in-Class · Orphan · Breakthrough · Priority Review · Accelerated

VERASTEM INC at a Glance

  • Fast trial execution (28 months median completion)

VERASTEM INC's Key Drugs

VERASTEM INC's core commercial portfolio centers on AVMAPKI FAKZYNJA CO-PACK (COPACKAGED), spanning Oncology — its most strategically important drugs approved in the last 15 years.

VERASTEM INC's Recent FDA Approvals

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

VERASTEM INC's Therapeutic Areas

VERASTEM INC'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 Phase 3: 1 Phase 2: 5 Phase 1: 11

VERASTEM INC's Top Competitors

VERASTEM INC'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.

VERASTEM INC Pipeline Snapshot

VERASTEM INC has 17 active clinical programs from ClinicalTrials.gov — 1 Phase 3, 5 Phase 2 and 11 Phase 1.

1
Phase 3
5
Phase 2
11
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q4 2028
avutometinib
Low Grade Serous Ovarian Cancer
Estimated · fresh NCT06072781

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

  • AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) 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: 0/1 completed
  • Speed: 28 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