lutetium lu 177 vipivotide tetraxetan
lutetium lu 177 vipivotide tetraxetan: 7 clinical trials tracked.
lutetium lu 177 vipivotide tetraxetan evidence translation
What we can confirm
7 tracked trials
What it means
What to watch
Prepared research question
What is verified about lutetium lu 177 vipivotide tetraxetan, and what remains unknown?
Traceable citations · Unknowns marked
See linked entities and source evidence2 indications · 0 study sponsors
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Clinical Trials (7)
Radioligand Efficacy Comparison by Initial PSA-Response Outcome in Metastatic CRPC With Lutetium 177Lu PSMA RLT (RECIPROCAL)
Primary endpoint: Overall survival (OS)
A Phase 2 Study of Biomarker-Modulated PSMA Theranostics
Primary endpoint: Prostate-specific antigen (PSA) progression-free survival (PFS)
PREcision DIagnostics in Prostate Cancer Treatment (PREDICT)
Primary endpoint: Objective Response
Vorinostat to Augment Response to 177Lutetium-PSMA-617 in the Treatment of Patients With PSMA-Low Metastatic Castration-Resistant Prostate Cancer
Primary endpoint: Proportion of patients who convert from prostate-specific membrane antigen (PSMA) low to PSMA high
Re-Treatment With 177Lu-PSMA-617 Molecular Radiotherapy for Metastatic Castration Resistant Prostate Cancer: A Prospective Phase 2 Trial (RE-LuPSMA STUDY)
Primary endpoint: 12-month overall survival
A Phase 2 Randomized Trial in Patients With Metastatic Castration Resistant Prostate Cancer to Determine the Efficacy of a Flexible Dosing Schedule of Lu-PSMA Treatment up to 12 Cycles Including Potential Treatment Holiday Periods in Comparison to the Standard Fixed Dosing Schedule of Six Cycles Every Six Weeks (FLEX-MRT)
Primary endpoint: 2-year survival rate
Phase I/II Study of CDK4/6 Inhibition With Abemaciclib to Upregulate PSMA Expression Prior to 177Lu-PSMA-617 Treatment in Patients With Metastatic Castrate Resistant Prostate Cancer (mCRPC) Previously Treated With Novel Hormonal Agents and Chemotherapy
Primary endpoint: Recommended phase 2 dose (Part A)