LSK BioPharma, a US-based biopharmaceutical firm, has entered into a global clinical collaboration with Jiangsu Hengrui Medicine Co. Ltd. (SHA:600276), an integrated biopharmaceutical company based in China, it was reported on Sunday.
The collaboration is aimed at evaluating the safety and efficacy of LSK BioPharma's rivoceranib, also known as apatinib or Aitan (brand name) in China, a selective and potent VEGFR-2 inhibitor, in combination with Hengrui's camrelizumab (SHR-1210), a humanised anti-PD-1 monoclonal antibody currently under NDA review in China for classic Hodgkin's Lymphoma in patients with advanced hepatocellular carcinoma. It is considered that the combination of rivoceranib and camrelizumab may enhance the immune system, aiding the fight against cancer. In addition to the known anti-angiogenic effects of rivoceranib, it may also enhance camrelizumab's anti-tumour activity by normalising tumour vasculature and reversing the tumour suppressive immune microenvironment.
According to the terms of the clinical collaboration agreement, Hengrui will be responsible for administering the clinical trial with all study costs outside China shared equally among both parties. LSK BioPharma will retain full commercial rights for rivoceranib outside China and Hengrui will retain full commercial rights for camrelizumab worldwide.
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Astrazeneca Imfinzi perioperative regimen gains positive EU CHMP opinion in early gastric cancer
I Peace generates human iPS cells from NKT cells and offers them for research use
Frontage expands early phase clinical research capabilities across US and China
Summit Therapeutics' BLA for ivonescimab in EGFR-mutated NSCLC accepted by FDA
InSysBio agrees new collaborative project with BeOne Medicines
Physiomics secures new modelling contract with Numab Therapeutics
Mabwell reports first patient dosed with 7MW4911 in US trial
Atossa Therapeutics' founder and CEO named one of The Top 50 Healthcare Technology CEOs of 2025
Avacta secures FDA clearance for second pre|CISION oncology programme
Guardant Health and Merck enter multi-year oncology diagnostics collaboration
Akeso secures NMPA review acceptance for gumokimab in ankylosing spondylitis