April 18 (Reuters) - Hyloris Pharmaceuticals SA
HYL.BR :
* REG-HYLORIS ANNOUNCES SUBMISSION OF MAXIGESIC® IV
PACKAGING DATA
REQUESTED BY THE US FDA
* RESULTS ANALYZED AND EVALUATED BY TOXICOLOGICAL EXPERTS
* POTENTIAL REGULATORY APPROVAL FOR MAXIGESIC® IV FOR THE US
MARKET BEFORE THE END OF 2023
* POTENTIAL REGULATORY APPROVAL FOR MAXIGESIC® IV FOR US
MARKET
BEFORE END OF 2023
* SALES COULD FOLLOW SOON AFTER, WITH AN EXCLUSIVE LICENSE
AND
DISTRIBUTION AGREEMENT ALREADY SIGNED BETWEEN AFT AND HIKMA
PHARMACEUTICALS ("HIKMA")
* UNDER TERMS OF DEVELOPMENT COLLABORATION AGREEMENT BETWEEN
HYLORIS AND AFT, HYLORIS IS ELIGIBLE TO RECEIVE A SHARE ON ANY
PRODUCT-RELATED REVENUES
Source text for Eikon: ID:nGNEmD1tp
Further company coverage: HYL.BR
(Gdansk Newsroom)
((gdansk.newsroom@thomsonreuters.com; +48 58 769 66 00;))