VS-7375
DrugTaken by mouth
NCT Number: NCT07644559
This study will assess the safety and efficacy of VS-7375 alone and in combination with cetuximab in patients with metastatic KRAS G12D - mutated Pancreatic Cancer
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 2
ICON Kurralta Park, Kurralta Park, South Australia, Australia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Adequate organ function
VS-7375 + cetuximab (2L PDAC) :
-Received only 1 prior Tx in the metastatic setting; prior adjuvant counts as a line if progressed within 6 months
VS-7375 + cetuximab (1L PDAC) :
-Treatment-naïve or received ≤ 1 cycle of SoC for metastatic disease
Exclusion criteria
Taken by mouth
Subcutaneous 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: 24 months
To evaluate additional efficacy parameters of VS-7375 monotherapy and VS-7375 in combination with cetuximab, administered on a daily oral schedule in participants with KRAS G12D-mutated PDAC.
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 pancreatic ductal adenocarcinoma patients
Time frame: 24 months
To assess the interval between initiation of study treatment and initiation of subsequent
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, as Monotherapy and With Cetuximab, in Patients With Metastatic KRAS G12D-Mutated Pancreatic Cancer (TARGET-D 201)
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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