South korea tracks Real-World safety of bladder cancer drug PADCEV
NCT ID NCT06011954
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study monitors 202 adults in South Korea with advanced bladder cancer who are receiving the drug PADCEV (enfortumab vedotin) as part of their normal care. Researchers will track side effects and how well the cancer responds for up to a year. No new treatment is given; the goal is to gather real-world safety and effectiveness data.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
Active substance
Enfortumab vedotin (PADCEV)
What this could lead to
If successful, this study will provide real-world safety and effectiveness data on PADCEV for advanced bladder cancer in South Korean patients.
What could go wrong
This is an observational study, not a controlled trial, so it cannot prove cause and effect. Results may be limited by small sample size and short follow-up.
Disclaimer
Read more
Show less
This is a summary of
the original study
.
Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for UROTHELIAL CANCER are added.
By submitting, you agree to our Terms of use
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
By submitting, you agree to our Terms of use
Study contacts
-
Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
-
Site KR82001
RECRUITINGGoyang-si, Gyeonggi-do, 10408, South Korea
-
Site KR82002
RECRUITINGSeoul, 02841, South Korea
-
Site KR82003
ACTIVE_NOT_RECRUITINGSeoul, 03722, South Korea
-
Site KR82004
ACTIVE_NOT_RECRUITINGIncheon, 21565, South Korea
-
Site KR82005
RECRUITINGSeoul, 03181, South Korea
-
Site KR82006
RECRUITINGSeoul, 07417, South Korea
-
Site KR82007
COMPLETEDJeollanam-do, Jeollanam-do, 58128, South Korea
-
Site KR82008
RECRUITINGSuwon, Gyeonggi-do, 16500, South Korea
-
Site KR82009
ACTIVE_NOT_RECRUITINGBusan, 49201, South Korea
-
Site KR82010
COMPLETEDBusan, 48108, South Korea
-
Site KR82011
RECRUITINGSeoul, 07985, South Korea
-
Site KR82012
RECRUITINGSuwon, Gyeonggi-do, 16247, South Korea
-
Site KR82013
RECRUITINGJeonju, Jeonbuk-do, 54907, South Korea
-
Site KR82014
RECRUITINGDaegu, 42415, South Korea
-
Site KR82015
ACTIVE_NOT_RECRUITINGBusan, 47392, South Korea
-
Site KR82016
COMPLETEDBusan, 50612, South Korea
-
Site KR82017
ACTIVE_NOT_RECRUITINGSeoul, 06351, South Korea
-
Site KR82018
RECRUITINGDaejeon, 35365, South Korea