PUMA BIOTECH
PharmaPUMA BIOTECH is a pharmaceutical company focused on Oncology, Gastroenterology. Key products include NERLYNX.
PUMA BIOTECH's Key Drugs
PUMA BIOTECH's core commercial portfolio centers on NERLYNX, spanning Oncology and Gastroenterology — its most strategically important drugs approved in the last 15 years.
PUMA BIOTECH's Recent FDA Approvals
New NDA/BLA approvals for PUMA BIOTECH over the last two years — novel drugs only, excluding generics and label supplements.
PUMA BIOTECH's Therapeutic Areas
PUMA BIOTECH's approved drugs and pipeline span 2 therapeutic areas, led by Oncology and Gastroenterology, across 0 biologic and 1 small-molecule drug. Weighted by commercial stage — approved drugs count most, then late-stage trials.
PUMA BIOTECH's Top Competitors
PUMA BIOTECH's closest competitors by therapeutic-area and drug-target overlap include Johnson & Johnson, Bristol-Myers Squibb, and Takeda. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.
PUMA BIOTECH Pipeline Snapshot
PUMA BIOTECH has 20 active clinical programs from ClinicalTrials.gov — 2 Phase 3, 9 Phase 2 and 9 Phase 1.
Pro Intelligence Preview
Deep insights for investors and analysts
Revenue Insights
- • NERLYNX leads revenue
- • Drug-level revenue analysis
Trial Catalysts
- • Oncology pipeline focus
- • Phase 3 readout tracking
Patent Risk
- • Patent expiration timeline
- • Revenue at risk analysis
Compare Companies
- • Side-by-side pipeline analysis
- • Revenue & market share comparison
Execution Intelligence
- • Phase 3: 2/2 completed
- • Speed: 52 months avg
Revenue forecasts • Trial milestones • Patent risk modeling
Active (1)
Discontinued (0)
Company Info
- First Approval
- 2017-07-17
- Latest
- 2021-06-28
- Applications
- 1
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 Trials that were terminated early, withdrawn, or suspended are not counted as completed—these often indicate safety issues, lack of efficacy, or strategic pivots.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- Fair (40-59%): Average execution, notable rate of terminated/withdrawn trials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