Oct 13 (Reuters) - XSpray Pharma AB (publ) XSPRAY.ST :
* XSPRAY PHARMA HAS OBTAINED RESULTS FROM BIOEQUIVALENCE
STUDIES
WITH HYNAP-DASA ANDA AND DECIDES TO FOCUS ON ITS IMPROVED
DASATINIB PRODUCT, DASYNOC™
* BIOEQUIVALENCE WITH REFERENCE PRODUCT SPRYCEL WAS ACHIEVED
IN
FED BUT NOT IN FASTING SUBJECTS DUE TO HIGH VARIABILITY OF
SPRYCEL
* TO FOCUS ENTIRELY ON IMPROVED VERSION, DASYNOC, WHICH HAS
ACHIEVED BIOEQUIVALENCE WITH A 30 PERCENT LOWER DOSE THAN
SPRYCEL
* TO END DEVELOPMENT OF GENERIC VERSION OF DASATINIB.
* SHORTER TIME IN PATENT WINDOW DECREASES IMPORTANCE OF
GENERIC
VERSION IN OUR PRODUCT PORTFOLIO
Source text for Eikon: ID:nMFNcfBLT7
Further company coverage: XSPRAY.ST
(Gdansk Newsroom)
((gdansk.newsroom@thomsonreuters.com; +48 58 7696600;))