Clinical trial
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
NCT05775406 is registered in ClinicalTrials.gov with Kymera Therapeutics, Inc. as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- 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
- Lead sponsor
- Kymera Therapeutics, Inc.
- Phase
- Phase 1
- Overall status
- Completed
- Start date
- May 15, 2023
- Completion date
- December 18, 2024
- Enrollment
- 52 (actual)
- Sites
- 11
Conditions
As the registry lists them; a condition with its own page is linked.
acute lymphocytic leukemia, advanced solid tumors, lymphomas, myeloid malignancies