RecruitingNCT07290270

Real-world Use of Lutetium (177Lu) Vipivotide Tetraxetan in China(PSMAreal CN)

Real-world Use of Lutetium (177Lu) Vipivotide Tetraxetan Injection in Metastatic Prostate Cancer: an Observational, Multicenter, Prospective Cohort Study in China (PSMAreal CN)


Sponsor

Novartis Pharmaceuticals

Enrollment

170 participants

Start Date

Feb 4, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

This non-interventional, observational, multicenter, prospective cohort study is designed to investigate the treatment patterns of mPC patients treated with lutetium (177Lu) vipivotide tetraxetan, as well as their clinical outcomes, real-world characteristics, and quality of life during the treatment period and up to one year after treatment completion.


Eligibility

Sex: MALEMin Age: 18 YearsMax Age: 99 Years

Plain Language Summary

Simplified for easier understanding

This real-world study tracks how a radioactive drug called lutetium-177 PSMA (used to treat advanced prostate cancer) is used and how well it works in patients across China in everyday clinical settings outside of a controlled trial. **You may be eligible if...** - You are an adult male diagnosed with metastatic castration-resistant prostate cancer (mCRPC) or metastatic hormone-sensitive prostate cancer (mHSPC) - Your doctor has decided to treat you with lutetium-177 PSMA as part of your normal care - You have adequate organ function as assessed by your medical team **You may NOT be eligible if...** - You are currently enrolled in another interventional clinical trial - You are already participating in another Novartis-sponsored non-interventional study using the same drug Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(1)

Novartis Investigative Site

Shanghai, Shanghai Municipality, China

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NCT07290270


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