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Clinical Trial Summary

This is a phase 1 study of FT522 administered with rituximab in participants with relapsed/refractory B-cell lymphoma (R/R BCL). The primary objectives of the study are to evaluate the safety and tolerability of FT522 in combination with rituximab, and to determine the recommended phase 2 dose (RP2D) of FT522 in combination with rituximab; each objective will be assessed with or without conditioning chemotherapy.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05950334
Study type Interventional
Source Fate Therapeutics
Contact Fate Trial Disclosure
Phone 866-875-1800
Email FateTrialDisclosure@fatetherapeutics.com
Status Recruiting
Phase Phase 1
Start date November 16, 2023
Completion date June 30, 2044

See also
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Recruiting NCT06445517 - Study Evaluating ISM8207 in Participants With Advanced Solid Tumors and Relapsed/Refractory B-Cell Lymphoma Phase 1