June 22 (Reuters) - Athira Pharma Inc ATHA.O :
* ATHIRA PHARMA ANNOUNCES TOPLINE RESULTS FROM ACT-AD PHASE
2
PROOF OF CONCEPT STUDY OF FOSGONIMETON IN MILD-TO-MODERATE
ALZHEIMER’S DISEASE
* ATHIRA PHARMA INC - PRIMARY ENDPOINT OF CHANGE IN
BIOMARKER ERP
P300 LATENCY WAS NOT STATISTICALLY SIGNIFICANT FOR FULL STUDY
POPULATION
* ATHIRA PHARMA INC - COMBINATION OF FOSGONIMETON AND
STANDARD-OF-CARE (ACHEIS) GIVEN TOGETHER SHOWED POTENTIAL
DIMINISHED EFFECT OF FOSGONIMETON
* ATHIRA PHARMA INC - FOSGONIMETON HAD A FAVORABLE SAFETY
PROFILE
OVER 26 WEEKS AND ACT-AD PROVIDES IMPORTANT LEARNINGS FOR
ONGOING LIFT-AD STUDY
* ATHIRA PHARMA INC - A PRE-SPECIFIED SUBGROUP ANALYSIS OF
PATIENTS ON FOSGONIMETON MONOTHERAPY SUGGESTS IMPROVEMENT IN ERP
P300 LATENCY AT WEEK 26
* ATHIRA PHARMA INC - A PRE-SPECIFIED SUBGROUP ANALYSIS OF
PATIENTS ON FOSGONIMETON MONOTHERAPY SUGGESTS IMPROVEMENT IN
ADAS-COG11 AT WEEK 26
Source text for Eikon: ID:nGNX68F5qR
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