Brief: Acucort Gets Approval To Start Bioequivalence Study For The US
Jan 23 (Reuters) - AcuCort AB ACUC.TE :
* ACUCORT OBTAINS REGULATORY APPROVAL TO START
BIOEQUIVALENCE
STUDY FOR THE US
* ANNOUNCES THAT CZECH STATE INSTITUTE FOR DRUG CONTROL,
SUKL HAS
APPROVED COMPANY'S APPLICATION TO CONDUCT FIRST OF TWO
BIOEQUIVALENCE STUDIES
* ARE PLANNED TO BE BASIS FOR A REGISTRATION APPLICATION FOR
COMPANY'S INNOVATIVE ALLERGY DRUG DEXA ODF IN UNITED STATES.
Source text for Eikon: ID:nWkrLqTp
Further company coverage: ACUC.TE
(Gdynia Newsroom)
((gdynia.newsroom@thomsonreuters.com; +48 587720920;))
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