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Re: Nemesis18 post# 678259

Wednesday, 03/13/2024 9:44:30 AM

Wednesday, March 13, 2024 9:44:30 AM

Post# of 822993
I was surprised some on the FDA review board already weighed in on Geron's application before the actual review. Thought that was a no-no??

>>The regulator said more treatment-emergent adverse events, serious adverse events and events leading to dose modification were observed in the imetelstat group compared to placebo in a phase 3 study in certain patients with myelodysplastic syndrome.

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