MELINTA
PharmaMELINTA is a pharmaceutical company focused on Infectious Disease, Dermatology, Gastroenterology. Key products include BAXDELA.
FDA Novel Drug Designations
(2017)See 1 novel approval →
MELINTA at a Glance
- Strong track record with 84% execution quality across 29 trials
- Fast trial execution (11 months median completion)
Upcoming FDA Decisions
Full Calendar →MELINTA's Key Drugs
MELINTA's core commercial portfolio centers on BAXDELA, spanning Infectious Disease and Dermatology — its most strategically important drugs approved in the last 15 years.
MELINTA's Recent FDA Approvals
New NDA/BLA approvals for MELINTA over the last two years — novel drugs only, excluding generics and label supplements.
MELINTA's Therapeutic Areas
MELINTA's approved drugs and pipeline span 3 therapeutic areas, led by Infectious Disease and Dermatology, across 0 biologic and 1 small-molecule drug. Weighted by commercial stage — approved drugs count most, then late-stage trials.
MELINTA's Top Competitors
MELINTA's closest competitors by therapeutic-area and drug-target overlap include APOTHECON, Pfizer, and PF PRISM CV. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.
MELINTA Pipeline Snapshot
MELINTA has 29 active clinical programs from ClinicalTrials.gov — 12 Phase 3, 10 Phase 2 and 7 Phase 1.
Pro Intelligence Preview
Deep insights for investors and analysts
Revenue Insights
- • BAXDELA leads revenue
- • Drug-level revenue analysis
Trial Catalysts
- • Infectious Disease 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: 9/11 completed
- • Speed: 11 months avg
Revenue forecasts • Trial milestones • Patent risk modeling
Active (1)
Discontinued (0)
Company Info
- First Approval
- 2017-06-19
- Latest
- 2023-12-01
- Applications
- 2
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 Trials that were terminated early, withdrawn, or suspended are not counted as completed—these often indicate safety issues, lack of efficacy, or strategic pivots.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