Aug 24 (Reuters) - Enlivex Therapeutics Ltd ENLV.TA :
* ENLIVEX ANNOUNCES REGULATORY CLEARANCE IN MULTIPLE
COUNTRIES FOR
INTEGRATION OF FROZEN ALLOCETRA FORMULATION AND EXPANSION OF
PATIENT POPULATION IN ITS SEPSIS PHASE II CLINICAL TRIAL
* ENLIVEX THERAPEUTICS LTD - SEPSIS PHASE II PROTOCOL
AMENDMENTS
HAVE BEEN CLEARED BY REGULATORY AUTHORITIES IN ISRAEL, SPAIN,
AND GREECE
* ENLIVEX THERAPEUTICS LTD - PLANS TO OBTAIN CLEARANCES FOR
PROTOCOL AMENDMENTS IN ADDITIONAL JURISDICTIONS
* ENLIVEX THERAPEUTICS LTD - SHELF LIFE OF FROZEN ALLOCETRA™
FORMULATION IS EXPECTED TO BE VASTLY SUPERIOR TO THAT OF ITS
LIQUID FORMULATION
* ENLIVEX - EXPECTS BROAD ACCEPTANCE OF PROPOSED AMENDMENTS
WILL
SHORTEN TIMELINE FOR POTENTIAL REGULATORY APPROVAL OF FROZEN
ALLOCETRA FORMULATION
* ENLIVEX - FROZEN FORMULATION OF ALLOCETRA EXPECTED TO HAVE
A
SHELF-LIFE SPANNING MULTIPLE YEARS, VERSUS SHELF LIFE OF 96
HOURS FOR LIQUID FORMULATION
* ENLIVEX - EXTENDED SHELF LIFE EXPECTED TO DRAMATICALLY
IMPROVE
MANUFACTURING SCALABILITY AND SHIPPING LOGISTICS WHILE REDUCING
PRODUCTION COSTS
Source text for Eikon: ID:nGNX6PDB4Y
Further company coverage: ENLV.TA
((Reuters.Briefs@thomsonreuters.com;))