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NCT05775406 · ClinicalTrials.gov registry record · Phase 1

Safety and Clinical Activity of KT-253 in Adult Patients with High Grade Myeloid Malignancies, Acute Lymphocytic Leukemia, Lymphoma, Solid Tumors

A Phase 1 study, sponsored by Kymera Therapeutics.

Completed
Registry status
Phase 1
Development phase
52
Enrollment target

NCT05775406 is a Phase 1 study that has completed, run by Kymera Therapeutics. The registered enrollment target is 52 participants.

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The verdict

NCT05775406, a Phase 1 study, has completed, sponsored by Kymera Therapeutics.

COMPLETED
Registry status
Phase 1
Development phase
52 participants
Enrollment target

Study Summary

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, myelofibrosis, and R/R solid tumors. The study will identify the pharmacologically optimal dose(s) (MTD) of KT-253 as the recommended Phase 2 dose (RP2D), based on all safety, PK, PD, and efficacy data.

Interventions

  • DRUG KT-253

Trial Details

FieldValue
Enrollment Target 52 participants
Start Date 2023-05-15
Est. Completion 2024-12-18
Phase Phase 1

Sponsor

Kymera Therapeutics

10 total trials

What the Registry Record Tells You About NCT05775406

The ClinicalTrials.gov registry entry for NCT05775406 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 52 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Kymera Therapeutics, which has 10 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which KT-253 is the first listed.

NCT05775406 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05775406 about?

NCT05775406 is a clinical study titled "Safety and Clinical Activity of KT-253 in Adult Patients with High Grade Myeloid Malignancies, Acute Lymphocytic Leukemia, Lymphoma, Solid Tumors". 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, myelofibrosis, and R/R solid tumo...

What is the current status of trial NCT05775406?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 52 participants. The study started on 2023-05-15. Estimated completion is 2024-12-18.

What interventions are being tested in trial NCT05775406?

The interventions under investigation include: KT-253 (DRUG).

Who is sponsoring clinical trial NCT05775406?

This trial is sponsored by Kymera Therapeutics, which has 10 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.