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NCT05225584 · ClinicalTrials.gov registry record · Phase 1

Safety, PK, PD, Clinical Activity of KT-333 in Adult Patients With Refractory Lymphoma, Large Granular Lymphocytic Leukemia, Solid Tumors

A Phase 1 study, sponsored by Kymera Therapeutics.

Completed
Registry status
Phase 1
Development phase
56
Enrollment target

NCT05225584 is a Phase 1 study that has completed, run by Kymera Therapeutics. The registered enrollment target is 56 participants.

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The verdict

NCT05225584, a Phase 1 study, has completed, sponsored by Kymera Therapeutics.

COMPLETED
Registry status
Phase 1
Development phase
56 participants
Enrollment target

Study Summary

This Phase 1a/1b study will evaluate the safety, tolerability and the pharmacokinetics/pharmacodynamics (PK/PD) of KT-333 in Adult patients with Relapsed or Refractory (R/R) Lymphomas, Large Granular Lymphocytic Leukemia (LGL-L), T-cell prolymphocytic leukemia (T-PLL), and Solid Tumors. The Phase 1a stage of the study will explore escalating doses of single-agent KT-333. The Phase Ib stage will consist of 4 expansion cohorts to further characterize the safety, tolerability and the pharmacokinetics/pharmacodynamics (PK/PD) of KT-333 in Peripheral T-cell Lymphoma (PTCL), Cutaneous T-Cell Lymphoma (CTCL), LGL-L, and solid tumors.

Interventions

  • DRUG KT-333

Trial Details

FieldValue
Enrollment Target 56 participants
Start Date 2022-05-19
Est. Completion 2025-03-03
Phase Phase 1

Sponsor

Kymera Therapeutics

10 total trials

What the Registry Record Tells You About NCT05225584

The ClinicalTrials.gov registry entry for NCT05225584 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 56 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-333 is the first listed.

NCT05225584 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05225584 about?

NCT05225584 is a clinical study titled "Safety, PK, PD, Clinical Activity of KT-333 in Adult Patients With Refractory Lymphoma, Large Granular Lymphocytic Leukemia, Solid Tumors". This Phase 1a/1b study will evaluate the safety, tolerability and the pharmacokinetics/pharmacodynamics (PK/PD) of KT-333 in Adult patients with Relapsed or Refractory (R/R) Lymphomas, Large Granular Lymphocytic Leukemia (LGL-L), T-cell prolymphocytic leukemia (T-PLL), and Solid Tumors. The Phase 1a...

What is the current status of trial NCT05225584?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 56 participants. The study started on 2022-05-19. Estimated completion is 2025-03-03.

What interventions are being tested in trial NCT05225584?

The interventions under investigation include: KT-333 (DRUG).

Who is sponsoring clinical trial NCT05225584?

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.