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: 17 Feb 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
- Phase II Solid tumours
Most Recent Events
- 10 Feb 2025 Updated long term efficacy data from the phase-III EV-302 trial in Urogenital cancer released by Pfizer
- 08 Jan 2025 Registered for Urogenital cancer (Combination therapy, First-line therapy, Late-stage disease, Metastatic disease) in China (IV)
- 28 Nov 2024 No recent reports of development identified for phase-I development in Bladder-cancer(Second-line therapy or greater) in USA (Intravesicular)