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Asianet Newsable on MSNRegeneron, Sanofi Say Their Inflammation Drug Approved By FDA For Rare Skin Disease ...The injection is now approved in the U.S. to treat eight distinct diseases with underlying type 2 inflammation.
Dupixent approved in the US as the only targeted medicine to treat patients with bullous pemphigoid Approval based on pivotal results showing improvements in sustained disease remission and ...
Anne Wojcicki, co-founder and former CEO of 23andMe, has bid to buy back the genetic testing platform, which was pronounced ...
The Food and Drug Administration approved the drug for adult patients with bullous pemphigoid, which mainly affects the ...
Regeneron and Sanofi are committed to helping patients in the U.S. who are prescribed Dupixent gain access to the medicine and receive the support they may need with the DUPIXENT MyWay® program. For ...
Dupixent approved in the US as the only targeted medicine to treat patients with bullous pemphigoid Approval based on pivotal results showing improvements in sustained disease remission and reductions ...
Regeneron Inc. seeks to disqualify Kirkland & Ellis from representing its opponent Novartis AG in a major antitrust and ...
This was the stock's second consecutive day of losses.
Regeneron Pharmaceuticals was outbid in its effort to buy 23andMe by a nonprofit led by the bankrupt genetics testing company’s co-founder. California-based TTAM Research Institute, led by Anne ...
A cyber attack on the genetic testing firm saw personal information of 155,592 UK residents accessed in a major cyber attack ...
Sanofi & Regeneron present positive results from EVEREST phase 4 study of Dupixent over Xolair in adults with severe CRSwNP and coexisting asthma at EAACI Congress: Paris Tuesday, ...
The agency cleared CSL’s hereditary angioedema drug days after “resource constraints” delayed a rival medicine. Elsewhere, ...
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