I hope you've stocked enough food and blankets because hellwill freeze over before we see a 3rd party review. Why would any authority validate Missling's submission? lol. It's just a delay tactic to continue his and his financial arm's lifestyle.
AVXL’s rational for using alternate methods for evaluating co-primary endpoints maybe explained here: NIH PUB
Evaluating co-primary endpoints collectively in clinical trials Often a treatment is assessed by co-primary endpoints so that a comprehensive picture of the treatment effect can be obtained. Co-primary endpoints can be different medical assessments angled at different aspects of a disease, therefore, are used collectively to strengthen evidence for the treatment effect. It is common sense that if a treatment is ineffective, the chance to show that the treatment is effective in all co-primary endpoints should be small.Therefore,it may not be necessary to require all the co-primary endpoints to be statistically significant at the 1-sided 0.025 levelto control the error rate of wrongly approving an ineffective treatment. Rather it is reasonable to allow certain variation for the p -values within a range close to 0.025. In this paper, statistical methods are developed to derive decision rules to evaluate co-primary endpoints collectively. The decision rules control the error rate of wrongly accepting an ineffective treatment at the level of 0.025 for a study and the error rate at a slightly higher level for a treatment that works for all the co-primary endpoints except perhaps one. The decision rules also control the error rates for individual endpoints. Potential applications in clinical trials are presented.