Drug data last refreshed 16h ago · AI intelligence enriched 5d ago
PADCEV (enfortumab vedotin) is an antibody-drug conjugate (ADC) targeting Nectin-4 for the treatment of metastatic urothelial carcinoma in patients who have previously received platinum-containing chemotherapy and a PD-1/PD-L1 inhibitor. It combines an anti-Nectin-4 monoclonal antibody with a microtubule-disrupting payload delivered directly to cancer cells.
The product is at peak commercial maturity with modest Part D uptake (133 claims in 2023), indicating a specialized niche indication requiring targeted medical and sales expertise.
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.
Enfortumab Vedotin, Pembrolizumab and Quemliclustat for the Treatment of Unresectable Locally Advanced and Metastatic Urothelial Cancer
Enfortumab Vedotin + Pembrolizumab Induction to Spare the Bladder in MIBC
Study of EV for Recurrent Endometrial Carcinoma
Study of GB-4362 With Enfortumab Vedotin and Pembrolizumab for Advanced Urothelial Cancer
Enfortumab Vedotin in Combination With Pembrolizumab vs. Concurrent Chemoradiotherapy (cCRT) in People With Muscle Invasive Bladder Cancer (EV-309)
Worked on PADCEV at Astellas? Share your interview experience or compensation data (+7 days Pro)
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.
Upgrade to Pro to access Medicare Part D spending data and other premium pharma intelligence.
Upgrade to Pro — $25/moWorking on PADCEV offers specialized experience in oncology, ADC biology, and second-line treatment algorithms in a niche indication. Medical Affairs roles dominate, reflecting the need for physician education and patient selection expertise rather than broad commercial expansion.
1 open roles linked to this drug