AstraZeneca is spending $100 million upfront to secure ex-China rights for an early-stage cancer drug developed by Jacobio Pharma.
The UK drugmaker will be responsible for advancing and selling the oral pan-KRAS inhibitor, JAB-23E73, in all markets except China, where it will co-develop and co-commercialize with Jacobio. The Beijing-headquartered biotech could get up to $1.9 billion in milestones, plus tiered royalties on future sales outside China, according to a Sunday
release
.
KRAS is one of the “most important oncogenes in cancer,” AstraZeneca’s head of early oncology and precision medicine Matt Hellmann said in the release. KRAS mutations play a role in a variety of tumor types, including pancreatic, colorectal and lung cancers, he added.
JAB-23E73 is currently in Phase 1 development in both the US and China, where it has shown “early signs of anti-tumor activity,” according to Jacobio. In China, the company is currently enrolling 334 patients with advanced solid tumors with a KRAS mutation in an open-label dose-escalation and dose-expansion Phase 1/2a trial. Data could come next year.
In the US, the company is signing up 294 patients with tumors, including colorectal cancer, pancreatic ductal adenocarcinoma, and non-small cell lung cancer (NSCLC), for a similar trial that might report in 2027.
The biotech developed the pill using its so-called Induced Allosteric Drug Discovery Platform, which uses computational and screening methods to pinpoint small molecules that can modify proteins.
Jacobio’s oncology efforts have caught the attention of several drugmakers. In August last year, Shanghai Allist Pharmaceuticals
licensed the China rights
for a KRAS G12C inhibitor and an SHP2 inhibitor from Jacobio. In 2020, AbbVie
licensed a suite
of SHP2 inhibitors from the biotech, though it returned them a few years later.
Not all of AstraZeneca’s recent developments in cancer have been positive. On Monday, the pharma
admitte
d
that a Phase 3 trial of Imfinzi in combination with the ATR kinase inhibitor ceralasertib had failed. The Imfinzi regimen didn’t significantly improve overall survival over the standard of care docetaxel in patients with locally advanced or metastatic non-small cell lung cancer. The company said it would share detailed results from the study, called LATIFY, at a future medical meeting.