CI

At a glance

ClinicalIndex Comparison Record
Phase 2Recruiting· 98 target
Drug / intervention
KN046 +1 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/NCT05985109
NCT05985109Phase 2RecruitingOn TrackUpdated 32mo ago

A Phase II Multi-cohort Clinical Study Evaluating The Efficacy and Safety of KN046 in Combination With Regorafenib for Metastatic Microsatellite-Stable Colorectal Cancer: a Phase II Multi-cohort Study

Peking University Cancer Hospital & Institute·interventional·Posted Aug 14, 2023·Updated Oct 26, 2023

In Brief

A Phase 2 clinical trial evaluating KN046 and regorafenib for Colorectal Cancer. Currently recruiting, targeting 98 participants across 1 site.

Detailed Summary

The study is an interventional Phase II clinical trial aiming to optimize immunotherapy strategies for microsatellite-stable colorectal cancer. We will include three types of metastatic colorectal cancer patients: those without liver metastasis, or carrying BRAF V600E mutation, or unable to tolerate chemotherapy as their initial or second-line treatment. The participants will receive a combination treatment of regorafenib and KN046 which is a PD-L1/CTLA-4 bispecific antibody. Treatment efficacy and safety profile would be evaluated in this study.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Phase 2Recruiting
2024202520262027
First PostedAug 14, 2023
Enrollment StartOct 26, 2023
Primary CompletionDec 31, 2026
TodayJul 1, 2026
Enrollment to primary: 3.2 yearsPosted 2.9 years agoPrimary completion in 6 months

Interventions

KN046drug

KN046 is a recombinant humanized PD-L1/CTLA-4 bispecific single-domain antibody that blocks both PD-L1 interaction with PD-1 and CTLA-4 interaction with CD80/CD86.

regorafenibdrug

Regorafenib is a multi-target tyrosine kinase inhibitors and is one of the standard third-line therapy in mCRC