Nice one, don't forget we also have Grunenthal onboard, but does any of the bench actually have input? While I'm sure they can offer some guidance as to the FDA approval process' the spotlight is firmly fixed on MSB to front the ODAC panel with there own expert team. When it comes to the science they will endure. Strings pulled by big pharma maybe.....given the groundbreaking consequence to the new treatment in the marketplace.
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FDA ODAC Meeting Material discussion analysis, page-114
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