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Re: None

Wednesday, 01/24/2024 6:37:44 PM

Wednesday, January 24, 2024 6:37:44 PM

Post# of 468479
So I open it up to the wider group. What stands in the way of NDA (FDA), AMA (TGA), and MAA (EMA) for the following indications: PDD, PD, AD, Adult Retts and Pediatric Retts. Would the three regulatory bodies reject the applications without review? Is there any medicine more efficaciously worth taking, functional in it's administration or tolerable with regards to side effects for any of these indications? If any one of these indications were approved it would change everything. Ignoring the application would risk the embarrassment of a rival regulator approving it.
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