March 31 (Reuters) - Kamada Ltd KMDA.TA :
* KAMADA ANNOUNCES TOP-LINE RESULTS FROM ITS PHASE 1/2
CLINICAL
TRIAL OF ITS PLASMA-DERIVED HYPERIMMUNE GLOBULIN (IGG) TREATMENT
FOR CORONAVIRUS DISEASE (COVID-19)
* KAMADA LTD - NO INFUSION-RELATED REACTIONS OR ADVERSE
EVENTS
CONSIDERED RELATED TO STUDY DRUG WERE OBSERVED
* KAMADA LTD - PRELIMINARY RESULTS DEMONSTRATED THAT IGG
LEVEL
INCREASE WAS ASSOCIATED WITH ENHANCED NEUTRALIZATION ACTIVITY
* KAMADA LTD - ONE PATIENT DIED ON DAY 37 POST-TREATMENT DUE
TO
COMPLICATIONS FROM COVID-19
* KAMADA LTD - THERE WERE TWO SERIOUS ADVERSE EVENTS IN
STUDY,
BOTH WERE CONSIDERED NOT RELATED TO STUDY DRUG
* KAMADA LTD - CONTINUE TO SUPPLY PRODUCT TO IMOH FOR
TREATMENT OF
COVID-19 PATIENTS IN ISRAEL
* KAMADA LTD - INITIAL ORDER FROM IMOH EXPECTED TO GENERATE
APPROXIMATELY $3.4 MILLION IN REVENUE FOR KAMADA
* KAMADA LTD - SCALED UP MANUFACTURING WILL SUPPORT
POTENTIAL
EXPANSION OF IMOH SUPPLY AGREEMENT, POSSIBLE DEMAND FROM
ADDITIONAL INTERNATIONAL MARKETS
Source text for Eikon: ID:nGNX99tbN5
Further company coverage: KMDA.TA
((Reuters.Briefs@thomsonreuters.com;))