FT576

FT576 in Subjects With Multiple Myeloma

What's the purpose of the trial?

To evaluate the safety and tolerability of FT576 when administered as monotherapy and in combination with daratumumab.

Trial status

Active, Not Recruiting

Phase
Phase 1
Enrollment
31
Last Updated
2 months ago
Patient Screener

Published Results

Explore published results and other resources associated with this clinical trial (including press releases, news articles and videos).

Interim Phase I Clinical Data of FT576 As Monotherapy and in Combination with Daratumumab in Subjects with Relapsed/Refractory Multiple Myeloma

Results: As of a data cutoff date of 18 Jul 2022, 9 patients with R/R MM were treated and evaluable for safety and efficacy, in the first 2 dose levels of Regimen A (n = 6) and in the first dose level of Regimen B (n = 3). No dose-limiting toxicities, and no events of any grade of cytokine release syndrome (CRS), immune effector cell-associated neurotoxicity syndrome, or graft-versus-host disease (GvHD), were observed.


Conclusions: Administration of a single dose of FT576 at 100 or 300 million cells/dose alone or in combination with daratumumab is safe and well tolerated thus far without CRS, neurotoxicity, or GvHD. Interim clinical data, including safety and tolerability and initial anti-tumor activity, from the ongoing Phase I dose-escalation study of FT576 will be presented at the conference.

1 year ago Read more

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