TLN-372 in Advanced KRAS Mutant Solid Tumors

Part of paid clinical trials in Birmingham, Alabama.

Sponsor
Treeline Biosciences, Inc.
Study ID
NCT07204340
Phase
PHASE1
Status
Recruiting

Conditions

  • KRAS Mutant Solid Tumors

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • TLN-372 — DRUG
    Specified dose on specified days
  • TLN-372 in combination with cetuximab — DRUG
    Specified dose on specified days
  • TLN-372 in combination with pembrolizumab — DRUG
    Specified dose on specified days

Study Details

The primary purpose of this study is to evaluate the safety, pharmacokinetics, and anti-tumor activity of TLN-372 as a single agent and in combination with other anti-tumor agents, in patients with advanced KRAS mutant solid tumors

Key Dates

Start date
Sep 29, 2025
Status verified
Apr 2026
Primary completion
Dec 3, 2031
Completion
Apr 1, 2032

Study Design

Enrollment
240 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT

Arms

  • Experimental: Single Agent
  • Experimental: Combination Treatment

Primary Outcome Measure

Number of patients experiencing adverse events (AEs) that meet protocol-defined dose-limiting toxicity (DLT) criteria following administration of TLN-372 [ Time Frame: Up to 2 years ]

Central Contacts

Locations (6)

FacilityCityStateZIPSite coordinators
University of Alabama at BirminghamBirminghamAlabama35294
Rebecca Arend
Dana-Farber Cancer InstituteBostonMassachusetts02215-5450
Kailene Sullivan
6176323482
START MidwestGrand RapidsMichigan49546
Principal Investigator
616-954-5554
Washington University Medical CampusSt LouisMissouri63108
Gina Vellequette
314-253-0616
Memorial Sloan Kettering Cancer CenterNew YorkNew York10021-3402
Jamie Walters
917-843-7966
Sarah Cannon Research InstituteNashvilleTennessee37203
Brittany Callaway
615-329-7283

Find similar trials in Birmingham, AL