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cadonilimab

Pharma & Biotech

Akeso adds B7-H3 to its ADC strategy, but AK157D1 enters a field where a rival is already under FDA review

China has cleared Akeso’s AK157D1 for Phase 1 testing in advanced solid tumors, adding a DXd-class B7-H3 programme to a target already attracting late-stage ADC competition.

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Pharma & Biotech

What the Akeso–INOVIO immunotherapy collaboration signals for the future of glioblastoma clinical research

Akeso and INOVIO test cadonilimab plus INO-5412 in the INSIGhT glioblastoma trial. Explore what this immunotherapy strategy could mean for GBM research.

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Pharma & Biotech

Akeso’s cadonilimab outperforms PD-1 inhibitors in real-world gastric cancer study

Cadonilimab outperforms PD-1 inhibitors in PD-L1-low gastric cancer patients. Find out what this means for global immunotherapy standards.

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Pharma & Biotech

Can Akeso’s cadonilimab unlock PD-L1-agnostic immunotherapy for gastric cancer patients?

Akeso Inc. has secured clearance from the United States Food and Drug Administration to initiate COMPASSION-37, a global Phase III trial evaluating cadonilimab, a first-in-class PD-1/CTLA-4 bispecific antibody, as part of a first-line treatment regimen for HER2-negative, unresectable or metastatic gastric and gastroesophageal junction adenocarcinoma. The randomized, multicenter trial will compare cadonilimab plus chemotherapy against

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