EMD SERONO
BiotechEMD SERONO is a biotechnology company focused on Oncology, Neurology, Immunology. Key products include BAVENCIO.
FDA Novel Drug Designations
(2017-2021)EMD SERONO at a Glance
- Fast trial execution (23 months median completion)
EMD SERONO's Key Drugs
EMD SERONO's core commercial portfolio centers on BAVENCIO, MAVENCLAD, TEPMETKO, spanning Oncology and Neurology — its most strategically important drugs approved in the last 15 years.
Metastatic Merkel cell carcinoma in adults and pediatric patients 12 years and older
Multiple Sclerosis
Metastatic non-small cell lung cancer (NSCLC) harboring mesenchymal-epithelial transition (MET) exon 14 skipping alterations.
EMD SERONO's Recent FDA Approvals
New NDA/BLA approvals for EMD SERONO over the last two years — novel drugs only, excluding generics and label supplements.
EMD SERONO's Therapeutic Areas
EMD SERONO's approved drugs and pipeline span 5 therapeutic areas, led by Oncology and Neurology, across 5 biologic and 2 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.
EMD SERONO's Top Competitors
EMD SERONO's closest competitors by therapeutic-area and drug-target overlap include Johnson & Johnson, Eli Lilly, and Roche. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.
EMD SERONO Pipeline Snapshot
EMD SERONO has 112 active clinical programs from ClinicalTrials.gov — 22 Phase 3, 34 Phase 2 and 56 Phase 1.
Pro Intelligence Preview
Deep insights for investors and analysts
Revenue Insights
- • BAVENCIO leads revenue
- • 3 key drugs tracked
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: 4/7 completed
- • Speed: 23 months avg
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 Trials that were terminated early, withdrawn, or suspended are not counted as completed—these often indicate safety issues, lack of efficacy, or strategic pivots.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