QTX3544 in Patients With Advanced Solid Tumors With KRAS G12V Mutations

Purpose

Phase 1 study to determine the safety, tolerability, and anti-tumor activity of QTX3544 as a single agent or in combination with cetuximab.

Condition

  • Advanced Solid Tumors

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Pathologically documented, locally advanced or metastatic malignancy with KRAS G12V mutations identified through molecular testing (NGS- or PCR-based) with a Clinical Laboratory Improvement Amendments-certified (or equivalent) diagnostic. - Part 1: Advanced solid tumors with at least one prior systemic therapy. - Evaluable and measurable disease per RECIST v1.1. - Part 2 and 3: Measurable disease per RECIST v1.1.

Exclusion Criteria

  • Active brain metastasis or carcinomatous meningitis - Significant cardiovascular disease - Active infection requiring intravenous (IV) antibiotics - Prior treatment with a KRAS inhibitor Other protocol-defined Inclusion/Exclusion Criteria may apply

Study Design

Phase
Phase 1
Study Type
Interventional
Allocation
Non-Randomized
Intervention Model
Sequential Assignment
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Part 1a: QTX3544 monotherapy dose escalation
QTX3544 will be administered at protocol defined dose based on cohort assignment
  • Drug: QTX3544
    QTX3544 will be administered at protocol defined dose.
Experimental
Part 1b: QTX3544 dose escalation in combination with cetuximab
QTX3544 will be administered at protocol defined dose in combination with cetuximab based on cohort assignment
  • Drug: QTX3544
    QTX3544 will be administered at protocol defined dose.
  • Combination Product: Cetuximab
    Cetuximab will be administered at protocol defined dose.
Experimental
Part 2: QTX3544 monotherapy dose expansion
QTX3544 will be administered at protocol defined dose based on cohort assignment
  • Drug: QTX3544
    QTX3544 will be administered at protocol defined dose.
Experimental
Part 3: QTX3544 dose expansion in combination with cetuximab
QTX3544 will be administered at protocol defined dose in combination with cetuximab based on cohort assignment
  • Drug: QTX3544
    QTX3544 will be administered at protocol defined dose.
  • Combination Product: Cetuximab
    Cetuximab will be administered at protocol defined dose.

Recruiting Locations

Sarah Cannon Research Institute
Denver 5419384, Colorado 5417618 80218
Contact:
Front Desk
720-754-2610
cann.ddudenvergeneral@sarahcannon.com

Yale Cancer Center
New Haven 4839366, Connecticut 4831725 06511
Contact:
Ingrid Palma
203-833-1034
ingrid.palma@yale.edu

Florida Cancer Specialists & Research Institute
Sarasota 4172131, Florida 4155751 34232
Contact:
Carly Taylor
941-377-9993
ctaylor@flcancer.com

South Texas Accelerated Research Therapeutics, LLC Midwest
Grand Rapids 4994358, Michigan 5001836 49546
Contact:
Olivia Sweeney
616-389-6674
olivia.sweeney@startresearch.com

Duke Cancer Center
Durham 4464368, North Carolina 4482348 27705
Contact:
Sabina Wlazlo Cascalheiro
919-613-4812
sabina.wlazlo@duke.edu

Sarah Cannon Research Institute
Nashville 4644585, Tennessee 4662168 37203
Contact:
Sarah Cannon Research Institute
844-482-4812
scri.ddureferrals@scri.com

The University of Texas MD Anderson Cancer Center
Houston 4699066, Texas 4736286 77030
Contact:
Ly M. Nguyen
832-794-3672
lmnguyen1@mdanderson.org

South Texas Accelerated Research Therapeutics, LLC San Antonio
San Antonio 4726206, Texas 4736286 78229
Contact:
Isabel Jiminez
210-593-5265
isabel.jimenez@startresearch.com

Huntsman Cancer Institute, University of Utah
Salt Lake City 5780993, Utah 5549030 84112
Contact:
Susan Sharry
801-585-3453
susan.sharry@hci.utah.edu

South Texas Accelerated Research Therapeutics Mountain Region, LLC
West Valley City 5784607, Utah 5549030 84119
Contact:
Marie Asay
801-907-4770
marie.asay@startresearch.com

More Details

NCT ID
NCT06715124
Status
Recruiting
Sponsor
Quanta Therapeutics

Study Contact

Quanta Therapeutics Clinical Trials
415-599-3892
clinicaltrials@quantatx.com