Aug 3 (Reuters) - Moberg Pharma AB (publ) MBPH.ST :
* APPROVAL IN EUROPEAN UNION REPRESENTS FIRST MARKETING
AUTHORIZATIONS FOR OUR NEW ONYCHOMYCOSIS TREATMENT WORLDWIDE
* NATIONAL APPROVALS ARE EXPECTED TO FOLLOW DURING UPCOMING
MONTHS
AND TIMELINES MAY VARY BETWEEN COUNTRIES
* IN CONNECTION WITH APPROVAL, IT WAS FOUND THAT ONLY ONE OF
OUR
TWO SUPPLIERS OF ACTIVE SUBSTANCE TERBINAFINE WAS APPROVED
* SHORT TERM WE THEREFORE HAVE A LIMITED SUPPLY OF
TERBINAFINE AND
ROLLOUT WILL BE A TWO-STEP PROCESS
* LAUNCH IN TWO STAGES MEANS THAT SIGNIFICANT EXPECTED
REVENUES
ARE POSTPONED AND BOD HAS THEREFORE RESOLVED ON A RIGHTS ISSUE
OF ABOUT SEK 100 MLN
Source text for Eikon: ID:nWkr7T5jTq
Further company coverage: MBPH.ST
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