CHIESI FARMACEUTICI SPA
BiotechCHIESI FARMACEUTICI SPA is a biotechnology company focused on Respiratory, Dermatology, Cardiovascular. Key products include MYALEPT.
FDA Novel Drug Designations
(2023)CHIESI FARMACEUTICI SPA at a Glance
- Fast trial execution (12 months median completion)
CHIESI FARMACEUTICI SPA's Key Drugs
CHIESI FARMACEUTICI SPA's core commercial portfolio centers on MYALEPT, LAMZEDE, ELFABRIO, spanning Respiratory and Dermatology — its most strategically important drugs approved in the last 15 years.
CHIESI FARMACEUTICI SPA's Recent FDA Approvals
New NDA/BLA approvals for CHIESI FARMACEUTICI SPA over the last two years — novel drugs only, excluding generics and label supplements.
CHIESI FARMACEUTICI SPA's Therapeutic Areas
CHIESI FARMACEUTICI SPA's approved drugs and pipeline span 5 therapeutic areas, led by Respiratory and Dermatology, across 1 biologic and 0 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.
CHIESI FARMACEUTICI SPA's Top Competitors
CHIESI FARMACEUTICI SPA's closest competitors by therapeutic-area and drug-target overlap include APOTHECON, CHIESI, and MALLINCKRODT. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.
CHIESI FARMACEUTICI SPA Pipeline Snapshot
CHIESI FARMACEUTICI SPA has 115 active clinical programs from ClinicalTrials.gov — 34 Phase 3, 41 Phase 2 and 40 Phase 1.
Pro Intelligence Preview
Deep insights for investors and analysts
Revenue Insights
- • MYALEPT leads revenue
- • 3 key drugs tracked
Trial Catalysts
- • Respiratory 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: 31/44 completed
- • Speed: 12 months avg
Revenue forecasts • Trial milestones • Patent risk modeling
Active (1)
Discontinued (0)
Company Info
- First Approval
- 2014-02-24
- Latest
- 2025-09-17
- Applications
- 3
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 Trials that were terminated early, withdrawn, or suspended are not counted as completed—these often indicate safety issues, lack of efficacy, or strategic pivots.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