RecruitingEN original

A Study to Survey Adults in South Korea With Cancer Who Receive PADCEV Injection

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This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.

About the trial

Enfortumab vedotin (or PADCEV Injection) is a treatment for cancer in the bladder lining (urothelial cancer). PADCEV Injection is now available to treat this cancer. People in this study will be adults in South Korea with locally advanced or metastatic urothelial cancer. Metastatic means the cancer has spread to other parts of the body. During their care, the person's doctor will have prescribed PADCEV Injection and other medicines to treat their cancer. People in the study will be treated according to their clinic's standard practice. This study is about collecting information only. This study will survey people who know they are receiving PADCEV Injection. The aims of the study are to check outcomes of treatment with PADCEV and record any medical problems during the study. Once a doctor has prescribed PADCEV Injection, a person in the study will be observed for up to 48 weeks (about 1 year) after their first dose. During this time, a person's medical records will be reviewed to check for any medical problems and to follow the condition of their cancer. If a person in the study stops taking PADCEV Injection sooner than 48 weeks, records will be reviewed until 30 days (1 month) after each person's last dose of PADCEV Injection or until they start a different medicine for their cancer.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • Pacjenci otrzymujący leczenie zastrzykami PADCEV zgodnie z zatwierdzoną lokalną etykietą leku

✗ Disqualifies

  • Pacjenci, u których PADCEV jest przeciwwskazany zgodnie z zatwierdzoną lokalną etykietą leku
  • Pacjenci otrzymujący lub planujący otrzymywać eksperymentalne leki w czasie obserwacji

Simplified criteria — AI translation

Trial details

Last updated (source)
July 8, 2026
Sex
No restrictions

Therapies / drugs in trial

Locations (18)

Site KR82001

Goyang-si, South Korea

Site KR82012

Suwon, South Korea

Site KR82008

Suwon, South Korea

Site KR82007

Jeollanam-do, South Korea

Site KR82013

Jeonju, South Korea

Site KR82015

Busan, South Korea

Site KR82010

Busan, South Korea

Site KR82009

Busan, South Korea

Site KR82016

Busan, South Korea

Site KR82014

Daegu, South Korea

Site KR82018

Daejeon, South Korea

Site KR82004

Incheon, South Korea

Site KR82002

Seoul, South Korea

Site KR82005

Seoul, South Korea

Site KR82003

Seoul, South Korea

Site KR82017

Seoul, South Korea

Site KR82006

Seoul, South Korea

Site KR82011

Seoul, South Korea

Trial contact

Astellas Pharma Global Development, Inc.

Contact information from ClinicalTrials.gov. Contact in English.

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/9/2026.

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