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The European Medicines Agency (EMA)’s safety committee has recommended measures to reduce the serious side effects linked with Janus kinase (JAK) inhibitors used to treat chronic inflammatory disorders. Read More
California is taking to the courts to challenge insulin pricing, charging that Eli Lilly, Novo Nordisk, Sanofi and three pharmacy benefit managers (PBMs) have conspired to set the price of insulin and to keep it on an ever-increasing trajectory. Read More
The FDA’s new pilot, the Biosimilar Regulatory Science Program, has gotten off the ground and has awarded grants for five projects that will explore ways to enhance biosimilar and interchangeable biosimilar product development and regulatory science. Read More
Airsupra is the result of a collaboration between AstraZeneca and UK-based Avillion, a drug development company that conducted the clinical studies. Read More
A new draft guidance from the FDA provides a variety of recommendations for the content of drug dosage and administration labeling, including information on dosage range, risks related to drug handling, concomitant treatments, specific populations and missed doses. Read More
A nonprofit physicians’ group has issued a statement calling for a full vetting of Eisai’s Alzheimer’s disease drug Leqembi (lecanemab) in an FDA advisory committee meeting before the agency makes any decision on full approval. Read More
Sandoz received bad news Tuesday when a federal appeals court affirmed the FDA’s decision to deny its challenge and grant Sanofi the exclusive right to market the blockbuster multiple sclerosis drug Aubagio. Read More
India-based Biocon Biologics has received a Complete Response Letter (CRL) from the FDA calling for more data on its biologics license application for a form of regular insulin (insulin-R) and evidence the company has resolved manufacturing problems uncovered in a preapproval inspection. Read More