NDAORALTABLETPriority Review
Approved
Jun 2025
Lifecycle
Growth
Competitive Pressure
0/100
Data completeness
3/8 — Basic
Priority Review
Drug data last refreshed 13h ago · AI intelligence enriched 3d ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
YEZTUGO (lenacapavir sodium) is an oral small-molecule tablet approved by the FDA on June 18, 2025. The drug's specific indication and mechanism of action are not yet detailed in available data, but it represents Gilead Sciences' entry into a new therapeutic area. This NDA approval signals a significant expansion of Gilead's portfolio beyond its established franchise areas.
Growth11.9 years to LOE
Early-stage growth product with minimal competitive pressure, suggesting a building commercial infrastructure and opportunity for foundational team roles.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Why This Matters for Your Career
Gilead Sciences is hiring 3 roles related to this product
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.