A Study to Evaluate the Efficacy and Safety of Inavolisib When Administered in Combination With Bevacizumab and FOLFOX or FOLFIRI as First Line Therapy in Participants With Colorectal Cancer
Megadott ok: Sponsor's decision
A legfontosabb adatok
- Fázis
- 2. fázis
A vizsgálat adatai
- Ki végzi
- Hoffmann-La Roche
- Azonosító
- NCT07323576EU 2025-523014-84-00
- A regiszteradat frissítve
- 2026. február 9.
- Eredeti leírás
This is a blinded Phase 2 study designed to evaluate the safety and efficacy of inavolisib with bevacizumab and chemotherapy, in participants with metastatic colorectal cancer (mCRC) whose tumors have a PIK3CA mutation. The study has a safety run-in period followed by a randomized period.A teljes eredeti leírásKevesebb
A Phase II, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Efficacy and Safety of Inavolisib With Bevacizumab Plus Folfox or Folfiri as First Line Therapy in Patients With PIK3CA-Mutated Metastatic Colorectal Cancer
This is a blinded Phase 2 study designed to evaluate the safety and efficacy of inavolisib with bevacizumab and chemotherapy, in participants with metastatic colorectal cancer (mCRC) whose tumors have a PIK3CA mutation. The study has a safety run-in period followed by a randomized period.
Bevonási feltételek: Eastern Cooperative Oncology Group (ECOG) <=1; Histologically confirmed adenocarcinoma originating in the colon or rectum of the Stage 4 ( treatment plan does not include resection or curative ablation) per American Joint Committee on Cancer (AJCC) v8; Measurable disease per RECIST v1.1; No prior systemic therapy in the metastatic setting; Confirmation of biomarker eligibility: documentation of a PIK3CA mutation from either central testing of tissue, or from a validated historically obtained (pre-existing) test of tumor tissue or blood may be used to confirm eligibility; Adequate hematologic and organ function within 14 days prior to initiation of study treatment; Agreement to adhere to the contraception requirements.
Kizáró feltételek: Residual Grade 2 or higher neuropathy due to prior oxaliplatin exposure (unless the participant is planned to be treated with FOLFIRI); History of gastrointestinal (GI) fistula, GI perforation, or intra-abdominal abscess within 6 months prior to Day 1 of Cycle 1; Treatment with strong cytochrome P450 (CYP) 3A4 inducers or strong CYP3A4 inhibitors within 1 week or 5 drug-elimination half-lives, whichever is longer, prior to initiation of study treatment (only for patients who will receive FOLFIRI); Type 2 diabetes requiring ongoing systemic treatment at the time of study entry or any history of Type 1 diabetes; Known HIV positive status with exceptions for well controlled and on stable treatment; History of malignancy within 5 years prior to screening, with the exception of the cancer under investigation in this study and malignancies with a negligible risk of metastasis or death; Biomarker eligibility as per definition; Symptomatic, untreated, or actively progressing CNS metastases.