A Phase 1/2a Study of VS-7375 in Patients With KRAS G12D-Mutated Solid Tumors

Eligibility Criteria

• * Individuals ≥18 years of age.
• * Agreement to sign and date an informed consent form (ICF) approved by the Institutional Review Board (IRB)/Independent Ethics Committee (IEC).
• * Histologic or cytologic evidence of locally advanced unresectable or metastatic solid tumor harboring a KRAS G12D mutation.
• * Must have received ≥1 prior line of standard systemic therapy for advanced or metastatic disease or experienced cancer progression within 6 months of neoadjuvant or adjuvant therapy.
• * Measurable disease according to Response Evaluation Criteria in Solid Tumors (RECIST) v1.1.
• * Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
• * Adequate organ function
• * Adequate cardiac function
• * Recovered from all AEs due to previous therapies to Grade ≤1 or baseline.
• * Agreement to use highly effective contraception
• * Underwent major surgical procedure as defined by the Investigator, other than for diagnosis, within 4 weeks prior to Cycle 1 Day 1,
• * Receipt of chemotherapy, targeted therapy, or radiotherapy (excluding palliative radiation) within 4 weeks or 5 half-lives, whichever is shorter, or immunotherapy within 4 weeks prior to Cycle 1 Day 1
• * Treatment with any investigational drug at least 4 weeks or 5 half-lives, whichever is shorter, prior to Cycle 1 Day 1.
• * History of treatment with direct and specific KRAS G12D inhibitors.
• * Symptomatic, untreated, or actively progressing known central nervous system (CNS) metastases.
• * Inability to swallow oral medications.
• * Evidence or history of uncontrolled, clinically significant hematological, renal, hepatic, endocrine, pulmonary, gastrointestinal, cardiovascular, psychiatric, coagulation, neurologic, dermatologic, autoimmune, or allergic disease
• * Individuals who are pregnant or breastfeeding.