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U.K.’s cost-effectiveness agency gives negative review of Alzheimer’s drug Leqembi 

August 22, 2024
Pharmalot Columnist, Senior Writer
Illustration: Alex Hogan/STAT; Photo: Eisai via AP

STAT+ | U.K.'s cost-effectiveness agency gives negative review of Alzheimer's drug Leqembi

The review from the U.K.'s cost-effectiveness watchdog means the Alzheimer's therapy wouldn't be available through the NHS.

By Andrew Joseph


STAT+ | Gene therapy pioneer Jim Wilson believes he can commercialize rare-disease drugs in a tough climate

As other firms are 'walking away, we can lean into this,' Wilson tells STAT, discussing launch of Gemma Biotherapeutics and Franklin Biolabs

By Jonathan Wosen


FDA approves updated Covid-19 vaccines, shots should be available in days

Pfizer and Moderna are set to begin shipping millions of doses. Novavax expects its updated vaccine version to be available a little later.

By Associated Press



Adobe

STAT+ | Tome Biosciences, once a high-flying gene-editing startup, is floundering

The company announced in December that it had raised $213 million to fund what it called the "final chapter in genomic medicines."

By Jason Mast and Allison DeAngelis


Opinion: In drug development, diversity must be extended to preclinical research

The FDA's draft guidance on diversity in clinical trials is good, but it overlooks the lack of diversity in preclinical research.

By Sophie Zaaijer


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