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Clinical Trial Summary

The study consists of the two parts, phase IIa and phase IIb.


Clinical Trial Description

The study consists of the two parts, phase IIa and phase IIb. Phase IIa study is to assess the safety and the antitumor activity in patients with mCRC and to recommend reasonable dosage regimen of HL-085 for phase IIb study. Phase IIb is a pivotal study to evaluate HL-085 plus Vemurafenib in patients with BRAFV600E mCRC whose disease has progressed after 1 or 2 prior regimens in the metastatic setting. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05233332
Study type Interventional
Source Shanghai Kechow Pharma, Inc.
Contact Zhimei Zhu, Master
Phone 86 215201345822
Email zhuzm@kechowpharma.com
Status Recruiting
Phase Phase 2
Start date February 24, 2022
Completion date July 20, 2024

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