The FDA last month accepted the application for subcutaneous Leqembi for maintenance dosing, with a target action date of ...

Q3 2024 Management View CEO Haruo Naito highlighted a 9% year-on-year revenue increase to 601.2 billion yen, with a focus on the pharmaceutical business driving growth. Key contributors included ...

Shares of BioArctic AB (STO:BIOA B) climbed 4.8% following the announcement of its partner Eisai's robust sales figures for ...

The FDA has approved the sBLA for once every 4 weeks lecanemab-irmb (Leqembi®) intravenous maintenance dosing.

Following the president’s recent executive order dismantling diversity, equity, and inclusion policies, the main page for the ...

In the latest development, the European Commission has asked the EMA's human medicines committee, the CHMP, to take a look at ...

A monthly 10 mg/mL maintenance dose of Leqembi had the same effects on mild Alzheimer’s symptoms as biweekly dose, research ...

Once every four weeks maintenance dosing may be easier for patients and care partners to continue treatmentAlzheimer's disease progression does ...

The monthly maintenance regimen, which offers a more convenient frequency than the initially approved treatment schedule for ...

Want to stay on top of the science and politics driving biotech today? Sign up to get our biotech newsletter in your inbox.

The reassessment of Leqembi’s safety data follows the agency’s previous recommendation of the drug for use in the EU.

The Japanese and American based pharma companies announced a win for their Alzheimer’s treatment, which has faced some negative backlash over the last year.