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

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NCT05225584

Sponsored by Kymera Therapeutics, Inc. (industry) · KYMR — their whole pipeline →.

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
56actual
Sites
13
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2022-05-19actualWhen the study began enrolling
Primary completion2025-03-03actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-03-03actualThe whole study's end, after follow-up
First posted2022-02-04actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-03-19actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Non Hodgkin Lymphoma (NHL)
  • Peripheral T-cell Lymphoma (PTCL)
  • Cutaneous T-Cell Lymphoma (CTCL)
  • Large Granular Lymphocytic Leukemia (LGL-L)
  • T-cell Prolymphocytic Leukemia (T-PLL)
  • Solid Tumors

Intervention

  • Drug: KT-333

Primary outcomes

what the primary-completion date above is the date OF
Safety
measured Safety will be assessed from the time ICF signature through 30 days post dose or prior to start of a new anticancer therapy
Safety
measured Safety will be assessed from the time ICF signature through 30 days post dose or prior to start of a new anticancer therapy
Safety
measured Safety will be assessed from the time ICF signature through 30 days post dose or prior to start of a new anticancer therapy
Maximum Tolerated Dose (MTD)
measured Within the first 28 days of treatment
Dose Limiting Toxicities (DLTs)
measured Within the first 28days of treatment

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