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Hutchison China, BeiGene Start Testing Surufatinib/Tislelizumab Combo In Solid Tumor Study


Benzinga | Mar 24, 2021 07:51AM EDT

Hutchison China, BeiGene Start Testing Surufatinib/Tislelizumab Combo In Solid Tumor Study

Hutchison China MediTech (NASDAQ: HCM) has initiated a Phase 1b/2 study of surufatinib combined with BeiGene Ltd's (NASDAQ: BGNE) tislelizumab in patients with advanced solid tumors in the U.S. and Europe.

* The open-label study will evaluate the safety, tolerability, pharmacokinetics, and efficacy of the surufatinib and tislelizumab combination.

* The study consists of two parts:

* Dose-finding Part 1 will be conducted to determine the recommended Phase II dose ("RP2D") and the maximum tolerated dose of surufatinib/ tislelizumab combo in patients with advanced or metastatic solid tumors who have progressed on, or are intolerant to, standard therapies.

* Part 2 dose expansion will be an open-label, multi-cohort design to evaluate the anti-tumor activity of surufatinib/tislelizumab combo in patients with specific types of advanced or metastatic solid tumors.

* Surufatinib is an oral angio-immuno kinase inhibitor that selectively inhibits the tyrosine kinase activity associated with vascular endothelial growth factor receptor and fibroblast growth factor receptor. It inhibits both angiogenesis and colony-stimulating factor-1 receptor, regulating tumor-associated macrophages, promoting the body's immune response against tumor cells.

* Tislelizumab (BGB-A317) is a humanized IgG4 anti-PD-1 monoclonal antibody specifically designed to minimize binding to Fc?R on macrophages.

* Price Action: HCM shares closed 0.1% higher at $28.04, and BGNE shares closed 5.8% lower at $335.39 on Tuesday.







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