Henlius’ EGFR-targeting ADC receives FDA clearance to enter clinic for solid tumors

Nov. 28, 2023

Shanghai Henlius Biotech Inc. has announced IND approval by the FDA for HLX-42 for injection, an antibody-drug conjugate (ADC) developed under a collaboration between Henlius and Medilink Therapeutics.

BioWorld Asia Regulatory Cancer Antibody-drug conjugate Immuno-oncology FDA IND

Today's news in brief

BioWorld

BioWorld briefs for Nov. 12, 2024.

Today's news in brief

BioWorld MedTech

BioWorld MedTech briefs for November 12, 2024.

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Sales balloon for GLP-1 drugs from Novo Nordisk, Eli Lilly

BioWorld

Nearly $3.8 billion was earned by Novo Nordisk A/S and Eli Lilly and Co. in the third quarter for their glucagon-like peptide-1 (GLP-1) drugs to treat obesity....

Regulatory actions for Oct. 31, 2024

BioWorld

Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Capsida, Electra,...

Australia reimburses Vazkepa a decade after US approval

BioWorld

For the first time, Australians have access to CSL Inc.’s Vazkepa (icosapent ethyl/Vascepa) for managing cardiovascular disease more than a decade after the drug...