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Re: Doc328 post# 431828

Wednesday, 09/20/2023 3:25:02 PM

Wednesday, September 20, 2023 3:25:02 PM

Post# of 462060
Quote: "This is very important and relevant guidance to address multiplicity. Until the last 5-6 years, almost all AD trials were in mild AD and with clinical rather than PET entry criteria. As the anti-amyloid drugs showed some activity in the mildest patients but no activity in the moderate patients, trials evolved to test either MCI (with proof of amyloid) only or Mild Ad / MCI (with proof of amyloid). ADAS-Cog is more sensitive to follow progression of mild AD than it is for MCI. Therefore, some studies the past 5 years have used CDR-SB (lecanemab among others as example) or iADRS (donanemab as only example). iADRS is basically the subset of ADAS-Cog found to be most sensitive for MCI and mild AD combined with the ADCS-iADL scale (a modified instrumental ADL for MCI and milder AD). Therefore the 2017 example for AD in the draft guidance became a poor example and not included in the final guidance to industry."

Good for you, Doc!

Is it fair to say that Anavex's (Dr. Jin's) newly released TLR for the 2b/3 results has a stronger chance of FDA approval than you initially thought?
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