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Adaptyv Bio reveals latest results in protein design competition

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RIO DE JANEIRO, Brazil — For the past two years, Adaptyv Bio has challenged the AI community to see how good today’s models are at designing proteins. Its latest competition, presented Monday at a top machine-learning …

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CellCentric raises $220M to get multiple myeloma pill to market

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CellCentric has reeled in a massive fund to help it address multiple myeloma patients who have exhausted all other treatment options.

The 22-year-old transatlantic biotech has collected a $220 million Series D to finish its …

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Novo Nordisk’s Q1 in four words: Pills, pricing, payments and pressure

Novo Nordisk’s Q1 in four words: Pills, pricing, payments and pressure

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A million patients with obesity are already taking Novo Nordisk’s Wegovy pill, CEO Mike Doustdar said Wednesday, despite the market entry of Lilly’s Foundayo.

Novo’s pill had sales of 2.3 billion Danish …​ ​Read More

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STAT+: Even at a meeting in Rome, FDA shifts are top of mind for gene therapy field

ROME — When Tim Hunt, who leads an organization for cell and gene therapy makers, reached for some reasons for optimism for the jittery field at a conference here last week, he highlighted the recent approvals of rare disease treatments from the likes of Rocket Pharmaceuticals and Regeneron Pharmaceuticals.

There was one other headline he touted as potentially promising: “FDA vaccine chief to leave the agency again.”

The allusion to Vinay Prasad — the Food and Drug Administration’s top regulator of gene and cell therapies as well as vaccines until his departure from the agency last week — was an indication that even at this event, designed to emphasize the opportunities and roadblocks the sector faces in Europe, it couldn’t escape the decisions that are coming from 4,500 miles away.

Continue to STAT+ to read the full story…

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ROME — When Tim Hunt, who leads an organization for cell and gene therapy makers, reached for some reasons for optimism for the jittery field at a conference here last week, he highlighted the recent approvals of rare disease treatments from the likes of Rocket Pharmaceuticals and Regeneron Pharmaceuticals.

There was one other headline he touted as potentially promising: “FDA vaccine chief to leave the agency again.”

The allusion to Vinay Prasad — the Food and Drug Administration’s top regulator of gene and cell therapies as well as vaccines until his departure from the agency last week — was an indication that even at this event, designed to emphasize the opportunities and roadblocks the sector faces in Europe, it couldn’t escape the decisions that are coming from 4,500 miles away.

Continue to STAT+ to read the full story…

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