Chinese biopharma Innovent Biologics (HKEX: 01801) and Xuanzhu Biopharma have entered into a clinical trial collaboration and supply accord for the combination therapies of Tyvyt (sintilimab) injection with KM-501, a novel HER-2 bispecific ADC, as potential treatment options for advanced solid tumors in China.
The agreement will see Innovent supply sintilimab for the collaborated clinical trial. Xuanzhu Biopharma, a subsidiary of Xuanzhu Biopharmaceutical, will conduct a Phase Ib clinical study to evaluate the anti-tumor activity and safety of the combination therapy of sintilimab with KM-501 in Chinese patients with advanced solid tumors. Innovent’s shares gained 2.5% to HK$41.55 on the news.
Tyvyt, which is licensed to US pharma major Eli Lilly (NYSE: LLY) for geographies outside of China, is an innovative PD-1 inhibitor that has been approved and included in the national reimbursement drug list (NRDL) for seven indications. It is also the only PD-1 inhibitor for the first-line treatment of five high-incidence cancer types in the NRDL.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze