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Study identifier: NCT06862219 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Safety Study of Enfortumab Vedotin in Indian Adults With Urothelial Cancer

Condition: Metastatic Urothelial Carcinoma  ·  Sponsor: Astellas Pharma Global Development, Inc.

PhasePhase 4
Planned participants100
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study is for Indian adults in India who have cancer in the bladder lining (urothelial cancer). Their cancer is advanced or has spread to other parts of the body. Enfortumab vedotin is a treatment for this type of cancer. The main aim of the study is to confirm the safety of enfortumab vedotin in Indian adults with urothelial cancer. During the study, people will receive enfortumab vedotin. The study treatment will be given to people slowly through a tube into a vein. This is called an infusion. People will receive 3 separate infusions of enfortumab vedotin in each 28-day (4 weeks) treatment cycle. People visit their study clinic for health-checks several times during and after they receive enfortumab vedotin.

This description comes directly from the study's public registry record.

Talk to the study team

Astellas Pharma Global Development, Inc.  ·  800-888-7704  ·  astellas.registration@astellas.com

Always discuss trial participation with your own doctor first.

Locations (13)

Site IN91013Patna, Bihar, IndiaRecruiting
Site IN91015Kochi, Kerala, IndiaRecruiting
Site IN91004Mumbai, Maharashtra, IndiaRecruiting
Site IN91016New Delhi, National Capital Territory of Delhi, IndiaRecruiting
Site IN91017Dumas, Surat, IndiaRecruiting
Site IN91007Vellore, Tamil Nadu, IndiaRecruiting
Site IN91005Varanasi, Uttar Pradesh, IndiaRecruiting
Site IN91006Kolkata, West Bengal, IndiaRecruiting
Site IN91012Ahmedabad, IndiaRecruiting
Site IN91010Bhubaneswar, IndiaRecruiting
Site IN91008Mumbai, IndiaRecruiting
Site IN91009Nagpur, IndiaRecruiting

+ 1 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06862219