This study will assess the safety and efficacy of VS-7375 alone and in combination with cetuximab or panitumumab and cetuximab plus mFOLFOX in patients with metastatic KRAS G12D - mutated Colorectal Cancer
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
150
START Los Angeles
Los Angeles, California, United States
RECRUITINGConfirmed ORR by blinded independent central review (BICR) per RESIST v1.1 - 2L CRC only
Overall Response Rate per RECIST version 1.1, per blinded independent central review (BICR)
Time frame: 6 months
To characterize the safety and tolerability of VS-7375 monotherapy or in combination with cetuximab or panitumumab, administered on a daily oral schedule in participants with KRAS G12D-mutated 2L+ CRC
Proportion/number of participants with AEs, TEAEs, TRAEs, SAEs, and dose interruptions/reductions and discontinuations
Time frame: 6 months
To characterize the safety and tolerability of VS-7375 in combination with cetuximab + mFOLFOX, administered on a daily oral schedule in participants with KRAS G12D-mutated 1L CRC
Proportion/number of participants with AEs, TEAEs, TRAEs, SAEs, and dose interruptions/reductions and discontinuations
Time frame: 6 months
Confirmed ORR per RECIST v1.1 assessed by BICR (primary) and Investigator (secondary) assessments
To evaluate additional efficacy parameters of VS-7375 monotherapy and VS-7375 in combination with cetuximab or panitumumab or cetuximab + mFOLFOX, administered on a daily oral schedule in participants with KRAS G12D-mutated CRC
Time frame: 24 months
Plasma Pharmacokinetics (PK) of VS-7375 and relevant metabolites, Cmax
Maximum concentration (Cmax)
Time frame: 20 weeks
Plasma Pharmacokinetics (PK) of VS-7375 and relevant metabolites, AUC
Area under plasma Concentration (AUC) 0 to t
Time frame: 20 weeks
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Intravenous infusion
Valkyrie Clinical Trials (contact for more locations)
Los Angeles, California, United States
RECRUITINGMoffitt Cancer Center
Tampa, Florida, United States
RECRUITINGIndiana University, Simon Comprehensive Cancer Center
Indianapolis, Indiana, United States
RECRUITINGSTART Midwest
Grand Rapids, Michigan, United States
RECRUITINGWashington University
St Louis, Missouri, United States
RECRUITINGSTART New Jersey
East Brunswick, New Jersey, United States
RECRUITINGSarah Cannon Research Institute Oncology Partners
Nashville, Tennessee, United States
RECRUITINGSTART Dallas Fort Worth
Fort Worth, Texas, United States
RECRUITINGThe University of Texas MD Anderson Cancer Center
Houston, Texas, United States
RECRUITING...and 7 more locations
To evaluate Pharmacodynamics (PD) and other relevant blood tumor markers specific to tumor type
CA19-9, CEA, CA-125
Time frame: Up to 2.5 years
To assess the health-related quality of life and disease based on European Organization for Research and Treatment of Cancer (EORTC) Quality of life Questionnaire Core module C30 (QLQ-C30)
The EORTC QLQ-C30 is a validated questionnaire to assess the quality of life of colorectal cancer patients
Time frame: 24 months
Time to next therapy
To assess the interval between initiation of study treatment and initiation of subsequent treatment
Time frame: 24 months