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Clinical Trial Summary

Exploratory study in adult males with metastatic prostate cancer intended to characterize the pharmacokinetics and biodistribution of PSMA-Targeted [In-111]-Labeled Trillium Compounds with and without the cytoprotective agent PTI-122. Up to 36 eligible subjects will be enrolled. Additional subjects may be enrolled if there is insufficient data for evaluation, for example if the original study subjects do not complete required imaging studies for reasons unrelated to adverse events. Up to four PSMA-Targeted [In-111]-Labeled Trillium Compounds will be evaluated. Each compound will be evaluated first without the cytoprotective agent, PTI-122, then the [In-111]-labeled Trillium Compound may be co-administered with PTI-122.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05773703
Study type Interventional
Source RatioThera
Contact John Babich, PhD
Phone 617-371-8898
Email jbabich@ratiotx.com
Status Recruiting
Phase Early Phase 1
Start date December 8, 2022
Completion date September 2023

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