KT-253

A Phase 1, Multicenter, Open-Label, Dose-Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Clinical Activity of Intravenously Administered KT-253 in Adult Patients With High Grade Myeloid Malignancies and Acute Lymphocytic Leukemia, Lymphoma and Advanced Solid Tumors

What's the purpose of the trial?

This Phase 1 study will evaluate the safety, tolerability, pharmacokinetics/pharmacodynamics (PK/PD), and clinical activity of KT-253 in adult patients with relapsed or refractory (R/R) high grade myeloid malignancies, acute lymphocytic leukemia (ALL), R/R lymphoma, and R/R solid tumors. The study will identify the pharmacologically optimal dose(s) of KT-253 as the recommended Phase 2 dose (RP2D), based on all safety, PK, PD, and efficacy data.
Trial status

Accepting patients

Phase
Phase 1
Enrollment
70
Last Updated
4 days ago
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Participating Centers

There are 10 centers participating in this trial. Enter a location below to find the closest center.

Experimental Treatments

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  • KT-253 is a kind of treatment called an MDM2 inhibitor. KT-253 may work by inhibiting proteins that cancer cells use to bypass the immune system to grow uncontrolled.

Arms / Cohorts

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Accepting patients

Arm A: Solid Tumors and Lymphomas

Accepting patients

Arm B: High Grade Myeloid Malignancies and ALL

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