Drug data last refreshed 16h ago · AI intelligence enriched 1mo ago
TRODELVY (sacituzumab govitecan) is an antibody-drug conjugate (ADC) that combines an anti-Trop-2 monoclonal antibody with the topoisomerase I inhibitor SN-38. It is approved for metastatic triple-negative breast cancer and other solid tumors where Trop-2 expression is present. The drug works by binding to Trop-2 on cancer cells and delivering cytotoxic payload intracellularly.
TRODELVY is in peak lifecycle stage with modest Part D adoption, suggesting the commercial team is scaling beyond launch phase but faces opportunities for expanded market penetration.
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
NeoAdjuvant Therapy Comparing Sacituzumab Govitecan+Pembrolizumab vs. SoC Chemotherapy in Clinical Stage II-III, Triple-negative Early Breast Cancer
Study of Sacituzumab Govitecan With Atezolizumab/Durvalumab as Maintenance Therapy for Extensive-Stage Small Cell Lung Cancer
A Trial to Evaluate Sacituzumab Govitecan in Combination With Endocrine Therapy in Patients With HR-positive, HER2-negative Metastatic Breast Cancer Progressed on CDK4/6 Inhibitors
Study of Naxitamab and Sacituzumab Govitecan in Patients With Metastatic Triple-negative Breast Cancer (TNBC)
A Study of Sacituzumab Govitecan in Combination With Cetuximab in People With Head and Neck Squamous Cell Cancer (HNSCC)
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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.
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Upgrade to Pro — $25/moTRODELVY careers span R&D, Medical Affairs, Regulatory Affairs, and Quality Assurance, reflecting the complexity of manufacturing and supporting an ADC therapeutic. Working on this product offers exposure to advanced modality science, oncology commercial strategy, and Gilead's global infrastructure.
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