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Re: 12x post# 429595

Thursday, 09/07/2023 8:12:03 AM

Thursday, September 07, 2023 8:12:03 AM

Post# of 463399
Right, I can't find an 8K in which Anavex discloses that both primary and secondary endpoints were met in the P2b/3 trial. Maybe I have overlooked it?

10-Q does as we know say:

ANAVEX®2-73 met the co-primary endpoints ADAS-Cog and ADCS-ADL and key secondary endpoint CDR-SB. ANAVEX®2-73 treatment slowed decline of cognition and function in patients with early Alzheimer’s disease over 48 weeks. Patients treated with ANAVEX®2-73 had 1.84 times higher odds, or likelihood, to improve cognitively compared to placebo, with a ADAS-Cog score threshold change of -0.5 points or better [Odds Ratio = 1.84 (p = 0.015)]. At clinically significant levels of improvement in function (ADCS-ADL score threshold change of +3.5 points or better), patients treated with ANAVEX®2-73 had 2.67 times higher odds, or likelihood, to improve function compared to placebo [Odds Ratio = 2.67 (p = 0.0255)]. Additionally, treatment with ANAVEX®2-73 reduced cognitive decline at end of treatment, measured with the ADAS-Cog, as compared to placebo, by 45%, representing a treatment difference in mean score change of -1.85 points (p=0.033). Compared to placebo, ANAVEX®2-73 reduced clinical decline of cognition and function by 27% with mean score difference of -0.42 points (p=0.040) as measured by the CDR-SB. ANAVEX®2-73 was generally safe and well tolerated. All statistical analyses were performed by outside consultancy companies.


But we are still missing the data showing that and the outcome measures here (ORs) are not per clincinicaltrials.gov either.

W must then assume for now that behind the scenes in the SAP the outcome measures are in fact ORs, but I remain sceptical on that until otherwise proven.

The longer we wait, the sooner we will get rich!

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