Drug data last refreshed 8h ago · AI intelligence enriched 3w ago
TRODELVY (sacituzumab govitecan) is an antibody-drug conjugate (ADC) developed by Gilead Sciences, approved in April 2020 for the treatment of certain cancers. It combines an anti-Trop-2 antibody with a topoisomerase I inhibitor payload, designed to deliver cytotoxic activity directly to tumor cells. The drug represents a precision oncology approach targeting Trop-2-positive malignancies.
At peak lifecycle stage with modest Part D utilization, indicating focused adoption in specialized oncology settings and potential for commercial team expansion.
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/moGilead Sciences is hiring 1 role related to this product
TRODELVY careers are concentrated in R&D, Medical Affairs, and QA functions, reflecting the drug's peak lifecycle stage and ongoing optimization needs. The 12 linked positions suggest moderate hiring activity, with emphasis on scientific and senior management roles to support market penetration and clinical evidence generation.
12 open roles linked to this drug