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Chinese cancer treatment shows survival edge in trial

By Zhang Chenxu | chinadaily.com.cn | Updated: 2026-08-26 11:40
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Chinese biotech firm Akeso Inc has announced positive interim results from a registrational Phase-3 trial, showing that its home-grown bispecific antibody ivonescimab combined with chemotherapy delivers statistically significant and clinically meaningful overall-survival benefits for patients with advanced biliary-tract cancer, compared with durvalumab plus chemotherapy.

Durvalumab plus chemotherapy is currently the globally-recognized standard-of-care first-line immunotherapy recommended by major international clinical guidelines for advanced BTC, an aggressive malignancy with limited treatment options and poor patient prognosis.

Conducted in a randomised, double-blind, multicentre setting, the study hit its pre-specified primary endpoint of overall-survival, as reviewed by an Independent Data Monitoring Committee.

All key secondary endpoints, including progression-free survival and objective response rate, were also achieved. Full detailed clinical data will be unveiled at upcoming international medical conferences and later published in peer-reviewed journals, the company said in a statement.

That means the trial, named as HARMONi-GI1, marks the first Phase-3 trial worldwide to yield a statistically superior OS outcome against this gold-standard PD-L1-based regimen for biliary-tract cancer, representing a landmark advance for this hard-to-treat tumour type.

“This statistically significant positive overall-survival result is a major breakthrough in biliary-tract cancer treatment,” said Michelle Xia, founder, chairwoman, president and CEO of Akeso.

According to Xia, HARMONi-GI1 is ivonescimab’s first successful Phase-3 readout within gastrointestinal oncology, building on four previously positive Phase-3 outcomes across lung-cancer indications.

The clinical potential of the PD-1/VEGF bispecific antibody is now expanding beyond lung malignancies to a wider spectrum of solid tumours.

“We strive to bring this innovative therapy to patients across the globe at the earliest possible time,” she added.

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