SENTI-202

SENTI-202-101: A Phase 1, Multicenter, Open-Label Study of SENTI-202, a Selective Off-the-Shelf Logic Gated CAR NK Cell Therapy, in Subjects With CD33 and/or FLT3 Expressing Hematological Malignancies

What will happen during the trial?

This is a dose-finding study of SENTI-202, comprised of an initial dose finding using a modified "3+3" study design to determine the maximum tolerated dose (MTD) and recommended phase two dose (RP2D) of SENTI-202 when administered after lymphodepleting chemotherapy (Part 1) followed by disease-specific expansion cohorts at the RP2D (Part 2).

More Information

Trial Status
Accepting patients
Trial Phase
Phase 1
Enrollment
21 patients (estimated)
Sponsors
Senti Biosciences
Tags
Natural Killer (NK) Cells (Allogeneic), CD33, FLT3
Trial Type
Treatment
Last Update
3 weeks ago
SparkCures ID
1857
NCT Identifier
NCT06325748

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