CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 53 enrolled
Drug / intervention
Pembrolizumab +2 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03475004
NCT03475004Phase 2Completed

Phase II Study of Pembrolizumab in Combination With Binimetinib and Bevacizumab in Patients With Refractory Colorectal Cancer

University of Colorado, Denver·interventional·Posted Mar 23, 2018·Updated Sep 19, 2024

In Brief

A Phase 2 clinical trial evaluating Pembrolizumab, Bevacizumab, and 1 other intervention for Colorectal Cancer and Metastatic Cancer. Completed, enrolled 53 participants across 1 site.

Detailed Summary

This is an open-label, single-center, single-arm phase II clinical trial evaluating the combination of pembrolizumab, binimetinib, and bevacizumab in patients with metastatic colorectal adenocarcinoma who have not responded to prior therapy.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
201820192020202120222023202420252026
First PostedMar 23, 2018
Enrollment StartSep 17, 2018
Primary CompletionApr 14, 2022
Study CompletionFeb 12, 2024
TodayJul 2, 2026
Enrollment to primary: 3.6 yearsPosted 8.3 years ago

Interventions

Pembrolizumabdrug

An intravenous, potent and highly selective humanized monoclonal antibody of the immunoglobulin G4 (IgG4)/kappa isotype designed to directly block the interaction between PD-1 and its ligands, PD-L1 and PD-L2.

Bevacizumabdrug

The pharmacokinetics of bevacizumab are characterized by a slow CL, long half-life, and a volume of distribution consistent with limited extravascular distribution.

Binimetinibdrug

Binimetinib (MEK162/ARRY-438162) is an orally bioavailable, small molecule selective and potent mitogen-activated protein kinase (MEK) 1 and MEK 2 inhibitor.