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

More Information

Trial Status
Accepting patients
Trial Phase
Phase 1
Enrollment
70 patients (estimated)
Sponsors
Kymera Therapeutics, Inc.
Tags
MDM2 Inhibitor
Trial Type
Treatment
Last Update
1 month ago
SparkCures ID
1828
NCT Identifier
NCT05775406

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