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Recruiting Phase 1, Phase 2 NCT07259590

NCT07259590 A Study of GFH375 Combined With Cetuximab or Chemotherapy in Participants With Solid Tumors Harboring KRAS G12D Mutation

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Clinical Trial Summary
NCT ID NCT07259590
Status Recruiting
Phase Phase 1, Phase 2
Sponsor Genfleet Therapeutics (Shanghai) Inc.
Condition Advanced Solid Tumors Cancer
Study Type INTERVENTIONAL
Enrollment 126 participants
Start Date 2025-10-21
Primary Completion 2027-07

Trial Parameters

Condition Advanced Solid Tumors Cancer
Sponsor Genfleet Therapeutics (Shanghai) Inc.
Study Type INTERVENTIONAL
Phase Phase 1, Phase 2
Enrollment 126
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2025-10-21
Completion 2027-07
Interventions
GFH375GFH375

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Brief Summary

This is a Phase Ib/II clinical study aimed at exploring the safety and efficacy of Regimen A (GFH375 in combination with Cetuximab) and Regimen B (GFH375 in combination with AG) in participants with solid tumors.Phase Ib: To evaluate the safety/tolerability and pharmacokinetic (PK) characteristics of GFH375 in combination with cetuximab or AG in participants with solid tumors, and to explore the efficacy of the combination therapy. Phase II: To evaluate the efficacy, safety/tolerability and PK characteristics of the combination therapy, and to explore the correlation between bio-marker and clinical efficacy.

Eligibility Criteria

Inclusion Criteria: 1. Voluntarily participate in the study and sign the informed consent form. 2. Participants receiving Regimen A must be ≥ 18 years old when signing the informed consent form, and participants receiving Arm B must be 18 - 75 years old. 3. Histologically or cytologically confirmed locally advanced unresectable or metastatic solid tumors, with KRAS G12D mutation. 4. Failed standard systemic treatment, or intolerant to standard treatment, or unsuitable for standard treatment, or no standard treatment available. 5. At least one measurable lesions according to RECIST v1.1 6. Participants receiving Regimen A must have an Eastern Cooperative Oncology Group Performance Status (ECOG PS) score of 0 - 2; participants receiving Regimen B must have an ECOG PS score of 0 - 1. 7. Have sufficient organ function. Exclusion Criteria: 1. Symptomatic brain metastasis, leptomeningeal metastasis, spinal cord compression, or primary brain tumor. 2. Presence of known coexisting other cancer

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