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Re: Drugdoctor post# 4088323

Monday, 03/20/2017 8:44:44 AM

Monday, March 20, 2017 8:44:44 AM

Post# of 4967026
GNMX 2.16 PHILADELPHIA, PA--(Marketwired - Mar 20, 2017) -

Trial did not meet primary endpoint (overall ADHD-RS), however showed encouraging trend in improvement at highest dose (400 mg BID)
Strong trend of efficacy in ADHD-RS inattention subscale (p=0.0515 vs placebo)
Strong trend of efficacy in ADHD-RS inattention subscale (p=0.0515 vs placebo)
Clear signal of efficacy and benefit to patients
ADHD-RS response rate 70% (p=0.0067 vs placebo)
CGI-I response rate 57% (p=0.0155 vs placebo)
ADHD-RS response rate 70% (p=0.0067 vs placebo)
CGI-I response rate 57% (p=0.0155 vs placebo)
Well tolerated with no serious adverse events
Conference call scheduled for 8:30 AM ET
http://finance.yahoo.com/news/aevi-genomic-medicine-provides-top-110000841.html


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