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RECRUITING
NCT06733441
PHASE1

A Study of TLN-254 in Participants With Relapsed or Refractory T-cell Lymphoma

Sponsor: Treeline Biosciences, Inc.

View on ClinicalTrials.gov

Summary

The primary purpose of this study is to evaluate the anti-tumor activity of TLN-254 monotherapy in participants with relapsed or refractory T-cell lymphoma.

Official title: Phase 1b, Randomized, Dose Optimization Study to Assess the Anti-Tumor Activity, Safety, and Pharmacokinetics of TLN-254 in Patients With Relapsed or Refractory T-cell Lymphoma

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

50

Start Date

2024-12-16

Completion Date

2028-11-15

Last Updated

2025-10-10

Healthy Volunteers

No

Conditions

Interventions

DRUG

TLN-254

TLN-254 will be administered orally at a specified dose on specified days depending on treatment allocation.

DRUG

TLN-254

TLN-254 will be administered orally at a specified dose on specified days.

Locations (5)

Stanford Cancer Institute

Stanford, California, United States

Washington University School of Medicine

St Louis, Missouri, United States

Memorial Sloan Kettering Cancer Center

New York, New York, United States

Sarah Cannon Research Institute

Nashville, Tennessee, United States

British Columbia Cancer Agency

Vancouver, British Columbia, Canada