Open-label, dose-confirmation and cohort expansion, multicenter, Phase Ib/II study to
assess the anti-tumor activity and safety of MEN1611 in combination with cetuximab for
the treatment of participants with phosphatidylinositol 3-kinase, catalytic, alpha
polypeptide gene (PIK3CA)-mutated metastatic colorectal cancer.
Additional locations may be listed on ClinicalTrials.gov for NCT04495621.
See trial information on ClinicalTrials.gov for a list of participating sites.
This Phase Ib/II study investigated the anti-tumor activity and safety of daily oral
doses MEN1611 in combination with cetuximab in female and male participants affected by
PIK3CA-mutated, neuroblastoma-Kristen-rat sarcoma virus (N-K-RAS) wild-type, and BRAF
wild-type metastatic colorectal cancer.
MEN1611 is a potent, selective class I phosphoinositide 3-kinase (PI3K) inhibitor. The
maximum tolerated dose of MEN1611 given as single agent was assessed in a Phase I trial
in participants with advanced solid tumors.
This Phase Ib/II started with a dose confirmation part (Step 1) to identify the
recommended phase 2 dose of MEN1611 given in combination with cetuximab.
The study continued with a cohort expansion (Step 2) to explore the anti-tumor activity
of the selected MEN1611 dose level combined with cetuximab with further assessment of
safety and tolerability.
Lead OrganizationMenarini Group