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SENTI-202: Off-the-shelf Logic Gated CAR NK Cell Therapy in Adults With CD33 and/or FLT3 Blood Cancers Including AML/MDS

SENTI-202: Off-the-shelf Logic Gated CAR NK Cell Therapy in Adults With CD33 and/or FLT3 Blood Cancers Including AML/MDS

Recruiting
18-74 years
All
Phase 1

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Overview

This is an open-label study of the safety, biodynamics, and anti-cancer activity of SENTI-202 (an off-the-shelf logic gated CAR NK cell therapy) in patients with CD33 and/or FLT3 expressing blood cancers, including AML and MDS.

Description

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).

Eligibility

Inclusion Criteria:

  • Subjects with CD33 and/or FLT3 expressing malignancies, including:
    • Relapsed refractory acute myeloid leukemia (AML) with morphologic relapse as defined by ≥5% bone marrow blasts who have received at least 1 prior line, but no more than 3 prior lines of standard anti-AML therapy. Subjects with FLT3-mutated or IDH ½-mutated disease must have received at least one prior targeted therapy.
    • Relapsed refractory myelodysplastic syndrome (MDS) with increased blasts who have received at least 1 prior line, but no more than 2 prior lines of anti-MDS therapy
    • Other hematological malignancies who have received at least 1 prior line of standard of care for the respective disease
    • Documentation of CD33 expression (or FLT3 expression if available) by individual institutional standard of care
  • ECOG performance score of 0-1
  • Adequate organ function including platelet count >20x109/L (platelet transfusion is permitted)
  • Adequate recovery from toxicities from previous cancer treatments, as described in the study protocol
  • Willing and able to provide written informed consent

Exclusion Criteria:

  • White blood cell (WBC) count of ≥20×109/L or circulating blasts ≥10×109/L or rapidly progressive/hyperproliferative disease
  • Acute promyelocytic leukemia with t(15;17) (q22;q12) or abnormal promyelocytic leukemia/retinoic acid receptor alpha (APML-RARA)
  • MDS with fibrosis (MDS-f) or known prior history of constitutional conditions/syndromes with chemo-responsive AML
  • Evidence of leukemic meningitis or known active central nervous system disease
  • Presence of extra-medullary disease or myeloid sarcoma alone with no morphologic hematologic relapse
  • Prior use of certain anti-cancer therapies and/or use within a certain number of days prior to SENTI-202 study treatment, as described in the study protocol
  • Hematopoietic cell transplantation (HCT) less than 100 days prior to the first dose of SENTI-202
  • Prior NK cell or CAR T cell therapy at any time
  • Prior donor lymphocyte infusion (DLI), except if after HCT for MRD+ disease
  • Medical conditions or medications prohibited by the study protocol
  • Pregnant or breastfeeding female

Study details
    AML/MDS
    CD33 Expressing Hematological Malignancies
    FLT3 Expressing Hematological Malignancies

NCT06325748

Senti Biosciences

16 June 2024

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