Summary
All participants with haematological and solid cancers who are enrolled in a parent study and were exposed to allgeneic CRISPR CAR T cellular therapy will be asked to participate in this long-term follow-up (LTFU) study.
Participants 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 participants with progressive disease or who receive a subsequent line of anti-cancer 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 therapy.