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Sanofi and Regeneron’s Dupixent (dupilumab) has been approved by the US Food and Drug Administration (FDA) for chronic ...
--U.S. FDA Delays: Sanofi is potentially exposed to any delays in reviews due to recently announced staff firings at the U.S. Food and Drug Administration. Its anti-inflammatory drug Dupixent was ...
The commitment to sustainability by Sanofi Canada has been hard to miss for anyone who’s visited the company’s 54-acre ...
The US Food and Drug Administration (FDA) has approved dupilumab (Dupixent) for the treatment of chronic spontaneous ...
The FDA had rejected the companies’ initial application in 2023, requesting additional data after the pharma firms reported ...
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Zacks Investment Research on MSNSanofi & Regeneron's Dupixent Receives FDA Nod for UrticariaSanofi SNY and partner Regeneron REGN announced that the FDA approved Dupixent (dupilumab) for the treatment of chronic ...
Dupixent, which was rejected by the FDA for chronic spontaneous urticaria in October 2023, is now approved as the first new ...
New Phase II data demonstrate amlitelimab’s efficacy in heterogeneous inflammatory asthma, as lunsekimig and itepekimab ...
Several states are reporting cases of measles, a highly contagious viral disease. Both children and adults can get measles.
A string of companies, including Sanofi India, Schaeffler India, CIE Automotive, and AMI Organics, will be in focus in the ...
China’s response to new United States (U.S.) tariffs could complicate the supply of important medicines, an analysis of data ...
Investors need to pay attention to important dates of the Stock split and record date to remain eligible and make necessary ...
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