BIOCRYST
PharmaBIOCRYST is a pharmaceutical company focused on Immunology, Oncology, Ophthalmology. Key products include RAPIVAB.
FDA Novel Drug Designations
(2020)See 1 novel approval →
BIOCRYST at a Glance
- Fast trial execution (13 months median completion)
BIOCRYST's Key Drugs
BIOCRYST's core commercial portfolio centers on RAPIVAB, ORLADEYO, spanning Immunology and Oncology — its most strategically important drugs approved in the last 15 years.
BIOCRYST News
All BIOCRYST news →- Nov 13, 2026 TrialsBioCryst Presents New Real-World Evidence Showing Reduced Angioedema-Related Medical Visits After Switching to ORLADEYO® (berotralstat) at ACAAI 2026 Annual Scientific Meeting ↗
- Nov 4, 2026 EarningsBioCryst Reports Third Quarter 2026 Financial Results ↗
- Oct 29, 2026 TrialsBioCryst to Present New Data for ORLADEYO® (berotralstat) and Navenibart at the 2026 American College of Allergy, Asthma & Immunology Annual Scientific Meeting ↗
- Oct 21, 2026 RegulatoryBioCryst Announces U.S. FDA Approval of ORLADEYO® 150 mg Oral Pellets for Adults and Adolescents with HAE ↗
- Aug 25, 2026 RegulatoryBioCryst Announces Approval of ORLADEYO® for Pediatric HAE Patients in Japan ↗
BIOCRYST's Recent FDA Approvals
BIOCRYST secured 1 new FDA approval for novel drugs (NDA/BLA) in the last two years.
BIOCRYST's Therapeutic Areas
BIOCRYST's approved drugs and pipeline span 4 therapeutic areas, led by Immunology and Oncology, across 0 biologic and 2 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.
BIOCRYST's Top Competitors
BIOCRYST's closest competitors by therapeutic-area and drug-target overlap include AbbVie, Pfizer, and Novartis. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.
BIOCRYST Pipeline Snapshot
BIOCRYST has 5 active clinical programs from ClinicalTrials.gov — 0 Phase 3, 3 Phase 2 and 2 Phase 1.
Pro Intelligence Preview
Deep insights for investors and analysts
Revenue Insights
- • RAPIVAB leads revenue
- • 2 key drugs tracked
Trial Catalysts
- • Immunology 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: 5/11 completed
- • Speed: 13 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