Enfortumab vedotin - Astellas Pharma/Pfizer
Alternative Names: AGS-22C3; AGS-22CE; AGS-22M6E; AGS-22ME; AGS-M6; ASG-22CE; ASG-22M6E; ASG-22ME; Enfortumab; Enfortumab vedotin-ejfv; PADCEVLatest Information Update: 26 Aug 2025
At a glance
- Originator Agensys; Seattle Genetics
- Developer Astellas Pharma; Astellas Pharma Global Development; Merck & Co; Seagen
- Class Antineoplastics; Auristatins; Drug conjugates; Immunoconjugates; Monoclonal antibodies
- Mechanism of Action Apoptosis stimulants; Mitosis inhibitors; Tubulin inhibitors; Tubulin polymerisation inhibitors
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Orphan Drug Status
Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.
- New Molecular Entity Yes
Highest Development Phases
- Marketed Urogenital cancer
- Phase III Bladder cancer
- Discontinued Solid tumours
Most Recent Events
- 26 Aug 2025 Discontinued - Phase-I for Bladder cancer (Second-line therapy or greater) in Canada, France, Germany, Spain, United Kingdom (Intravesicular) (Astellas pipeline, August 2025)
- 26 Aug 2025 Discontinued - Phase-II for Solid tumours (Late-stage disease, Second-line therapy or greater, Metastatic disease) in USA, Japan, Canada (IV) (Astellas pipeline, August 2025)
- 13 Aug 2025 Efficacy data from a phase III trial in Bladder cancer released by Pfizer and Astellas Pharma