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Clinical Trial Summary

This study will evaluate the long-term safety and efficacy of CRISPR CAR T cellular therapies


Clinical Trial Description

All subjects with hematological and solid malignancies who are enrolled in a parent study and were exposed to allogeneic CRISPR CAR T cellular therapy will be asked to participate in this long-term follow-up (LTFU) study. Subjects who have completed the parent study for the protocol-defined duration, or who have discontinued the parent study early, or who are in secondary follow-up (follow up of subjects with progressive disease or who receive a subsequent line of anticancer therapy) in the parent study may enroll in this LTFU study. This will allow for collection of long-term efficacy data (as applicable) and safety data up to 15 years post-treatment with CRISPR CAR T cellular therapies. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06208878
Study type Observational
Source CRISPR Therapeutics
Contact
Status Enrolling by invitation
Phase
Start date November 22, 2023
Completion date August 2038

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