Biopharmaceutical company AstraZeneca plc (STO:AZN) (LON:AZN) (NYSE:AZN) announced on Tuesday that it has agreed to invest USD2bn in newly issued equity in biopharmaceutical oncology company Summit Therapeutics Inc (NASDAQ:SMMT) to accelerate the development of ivonescimab, a PD-1/VEGF bispecific antibody, in combination with antibody drug conjugates (ADCs) across tumour types.
The companies will initially collaborate on clinical trials evaluating sonesitatug vedotin (Sone-Ve), a potential first-in-class Claudin-18.2-targeting ADC, with ivonescimab in gastrointestinal cancers.
Under the agreement, AstraZeneca and Summit will each provide their respective medicines and jointly fund trial costs, while retaining development and commercial rights to their own products.
The companies also signed a memorandum of understanding covering a planned global development programme combining ivonescimab with AstraZeneca's cancer medicines, including additional ADCs.
AstraZeneca recently reported positive high-level results from the CLARITY-Gastric01 trial of Sone-Ve in second-line and later Claudin18.2-positive advanced gastric cancer, with the results due to be presented at the European Society for Medical Oncology Congress 2026.
Ivonescimab, engineered by biopharmaceutical company Akeso Inc (HKEX: 9926), combines PD-1 blockade with VEGF inhibition and is approved for certain non-small cell lung cancer patients in China, while a US FDA application for EGFR-mutated NSCLC is under review. Summit holds exclusive rights to develop and commercialise ivonescimab in major territories outside China, with Akeso retaining rights in China and other regions.
AstraZeneca will receive approximately 109,000 preferred shares convertible into common stock at a 1:1,000 ratio, giving it rights equivalent to approximately 12.0% of Summit's outstanding common stock, or about 10.6% on a fully diluted basis. Closing of the investment is expected within one week.
Sone-Ve is continuing development in Phase III and Phase II trials across gastric, gastroesophageal junction, oesophageal adenocarcinoma, pancreatic and biliary tract cancers.
Precigen announces FDA platform technology designation for AdenoVerse
Kelun-Biotech publishes phase III data for trastuzumab botidotin in HER2-positive breast cancer
GSK reports positive Jideytro data supporting potential first-line lung cancer use
Akeso presents positive results from registrational Phase III study of ivonescimab
Insilico Medicine doses first patient in Phase III trial of rentosertib
Altesa BioSciences presents positive vapendavir clinical data at ERS International Congress 2026
Akeso's ivonescimab meets overall survival endpoint in interim analysis of Phase III HARMONi-2 study
AstraZeneca completes global licence agreement for Zegfrovy
Kazia Therapeutics reports 100% clinical benefit rate in initial paxalisib breast cancer trial
Oxcia receives EMA orphan designation for OXC-201 in idiopathic pulmonary fibrosis
Cizzle Bio presents CIZ1B biomarker blood test for lung cancer at Next Generation Dx Summit
Maverix Medical's Narwhal Cryo System receives FDA 510(k) clearance
Vascarta commences NIH phase I clinical study of VAS-101 in sickle cell disease