 Last Update: Jul 06, 2026 

 A Post Marketing Surveillance on PluvictoTM (Lutetium(177Lu) Vipivotide Tetraxetan) in South Korea; An Open-label, Non-interventional, Primary Data Collection, Multi-center, Non-comparative, Non-randomized Observational Study to Assess Safety and Effectiveness of Pluvicto in Real World Setting 

ClinicalTrials.gov Identifier: [NCT06514521](https://clinicaltrials.gov/ct2/show/NCT06514521)

 

Novartis Reference Number:CAAA617A1KR01

 

 [See if you Pre-qualify](#trial-eligibility "See if you Pre-qualify") 

 All compounds are either investigational or being studied for (a) new use(s). Efficacy and safety have not been established. There is no guarantee that they will become commercially available for the use(s) under investigation. 

 

##  Study Description 

Post marketing study on Pluvicto in Korea This is open-label, multi-center, non-comparative, non-interventional observational study to assess safety and effectiveness of Pluvicto in patients with mCRPC in the real-world setting in South Korea.



 

 Condition Metastatic Castration-resistant Prostate Cancer 

 

 Overall Status Recruiting 

 

 Number of Participants278

 

 

 Start Date Apr 18, 2025 

 

 Completion Date May 31, 2028 

 

 Gender Male 

 

 Age(s) 18 Years - 100 Years (Adult, Older Adult) 

 

 

 

##  Interventions 

Other

### Lutetium vipivotide tetraxetan



This is an observational study. There is no treatment allocation. The decision to initiate Lutetium vipivotide tetraxetan will be based solely on clinical judgement.

 



 

 

 

##  Eligibility Criteria 

Inclusion criteria

Study participants eligible for inclusion in this study must meet all of the following criteria:

1\. Male adult patient age ≥ 18  
2\. Subject who are being treated with Pluvicto or whose treatment plan is finalized and scheduled to be administered at the time of consent by physician in accordance with the approved indication in South Korea  
3\. Subject who provided the written informed consent prior to the study enrollment

Exclusion criteria

Study participants meeting any of the following criteria are not eligible for inclusion in this study:

1\. Subject whose medical record is not accessible  
2\. Subject who is not willing to provide the informed consent



 

 South Korea 

####  Novartis Investigative Site 

Recruiting

 Seongnam-si,Gyeonggi-do,13620,South Korea

 

 

 

 

####  Novartis Investigative Site 

Recruiting

 Gyeonggi-do,Korea,10408,South Korea

 

 

 

 

####  Novartis Investigative Site 

Recruiting

 Seoul,Seoul,06351,South Korea

 

 

 

 

####  Novartis Investigative Site 

Recruiting

 Seoul,03722,South Korea

 

 

 

 

####  Novartis Investigative Site 

Recruiting

 Seoul,05505,South Korea

 

 

 

 

####  Novartis Investigative Site 

Recruiting

 Seoul,06591,South Korea

 

 

 

 

####  Novartis Investigative Site 

Recruiting

 Seoul,110-744,South Korea

 

 

 

 

####  Novartis Investigative Site 

Recruiting

 Suwon,Gyeonggi-do,442-723,South Korea

 

 

 

 

####  Novartis Investigative Site 

Recruiting

 Busan,Korea,46033,South Korea

 

 

 

 

####  Novartis Investigative Site 

Recruiting

 Seoul,Seoul,03374,South Korea

 

 

 

 

####  Novartis Investigative Site 

Recruiting

 Seoul,01812,South Korea

 

 

 

 

####  Novartis Investigative Site 

Recruiting

 Jeollanam,519763,South Korea

 

 

 

 

 

 

 

 

 

##  Worldwide Contacts 

If the location of your choosing does not feature any contact detail, please reach out using the information below.

#### Novartis Pharmaceuticals

Phone: [ +41613241111](tel:+41613241111) 

Email: <novartis.email@novartis.com>