VS-7375
DrugTaken by mouth
NCT Number: NCT07659795
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
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 2
Icon Cancer Centre South Brisbane, South Brisbane, Queensland, Australia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
2L+ patients:
1L patients:
Exclusion criteria
Taken by mouth
Intravenous infusion
Intravenous infusion
Intravenous infusion
Time frame: 6 months
Overall Response Rate per RECIST version 1.1, per blinded independent central review (BICR)
Time frame: 6 months
Proportion/number of participants with AEs, TEAEs, TRAEs, SAEs, and dose interruptions/reductions and discontinuations
Time frame: 6 months
Proportion/number of participants with AEs, TEAEs, TRAEs, SAEs, and dose interruptions/reductions and discontinuations
Time frame: 24 months
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: 20 weeks
Maximum concentration (Cmax)
Time frame: 20 weeks
Area under plasma Concentration (AUC) 0 to t
Time frame: Up to 2.5 years
CA19-9, CEA, CA-125
Time frame: 24 months
The EORTC QLQ-C30 is a validated questionnaire to assess the quality of life of colorectal cancer patients
Time frame: 24 months
To assess the interval between initiation of study treatment and initiation of subsequent treatment
Time frame: 24 months
To assess tumor metabolism dynamics on FDG-PET/CT
Contact information is provided by the study sponsor or research team.
Verastem, Inc.
Industry
A Phase 2, Open-label Study of VS-7375, an Oral KRAS G12D (ON/OFF) Inhibitor, With and Without an Anti-EGFR Antibody, and With an Anti-EGFR Antibody and Chemotherapy, in Patients With Metastatic KRAS G12D-Mutated Colorectal Adenocarcinoma (TARGET-D 203)
Acronym: TARGET-D 203
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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