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Clinical Trial Summary

At the completion of primary follow-up of various Medeor Transplant studies (called parent studies), subjects receiving Medeor's cellular immunotherapy products will be followed annually for up to an additional 84 months (7 years), in order to evaluate for long-term safety.


Clinical Trial Description

Study MDR-105-SAE is intended to be the long-term safety monitoring extension of Medeor's cellular immunotherapy, kidney transplant clinical studies. This Master Protocol has been created in order to establish a single database for all long-term safety data for those subjects that have received Medeor's cellular products. This Master Protocol will provide up to 84 months (7 years) of additional follow-up. Long-term safety of subjects treated with Medeor's cellular immunotherapy has not been assessed. This study will collect the data into a centralized database allowing for continuous monitoring of any important safety signals. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05010174
Study type Observational
Source Medeor Therapeutics, Inc.
Contact Lenuta Micsa, MD
Phone 646-239-9748
Email lmicsa@medeortx.com
Status Recruiting
Phase
Start date May 11, 2022
Completion date December 2031

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