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Re: growingpain post# 390952

Friday, 12/09/2022 7:36:52 AM

Friday, December 09, 2022 7:36:52 AM

Post# of 468280
That's where SPA (agreement with FDA and other regulatory authorities) comes in. In a SPA, the company (say Anavex) negotiates with FDA to specify the primary endpoints and secondary endpoints. If there is no SPA, primary endpoints can be changed as a company wishes. When the agreed benchmarks are reached under a SPA, FDA will accept an NDA. FDA will consider drugs not under a SPA (273). The process is just very long and may require a more "experienced" partner.
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