HHS is asking the court to affirm its Office of Inspector General's finding that paying for fertility services would run ...

The FDA also approved Qiagen's Therascreen KRAS RGQ PCR kit as a companion diagnostic to identify KRAS G12C-mutant patients.

Despite Leqembi's initial slow sales, the firm's CEO cited areas for the drug's growth and ambitions for an antisense ...

The firm will pay $45 million upfront for several new targeted agents that it plans to pair with isotopes to develop both ...

The company anticipates launching three CRISPR products by 2030, including therapies for hereditary angioedema and ...

This marks the first US approval for AstraZeneca and Daiichi Sankyo's Trop-2-directed antibody drug conjugate.

Researchers from the Broad Institute, Mass General, Stanford, and elsewhere are investigating why patients with South Asian ...

Although Pfizer is not among the drugmakers suing the government to block negotiations, it has said the program will hinder drug R&D and innovation.

NEW YORK – Context Therapeutics on Wednesday said it began treating patients in a Phase I trial of its claudin 6 (CLDN6)- and CD3 T-cell-engaging bispecific antibody, CTIM-76, in CLDN6-positive ...

The firm, which plans to use the ticker symbol "MAZE" on the Nasdaq, develops drugs designed to mimic the protective effects ...

NEW YORK – The US Department of Health and Human Services' Office of Inspector General posted a report Tuesday outlining recommendations to improve consistency and transparency in the US Food and Drug ...

NEW YORK – When the US Food and Drug Administration approved Tecelra (afamitresgene autoleucel) in August 2024 for certain patients with advanced sarcoma, Adaptimmune became the second company to ever ...