Aug 26 (Reuters) - MEDESIS PHARMA SA ALMDP.PA :
* WAS INFORMED BY ANSM ON REFUSAL TO AUTHORIZE CLINICAL
STUDY OF
ITS NANOMANGANESE
* STUDY OF NANOMANGANESE WAS SUPPOSED TO INVESTIGATE
TREATMENT OF
SEVERE FORMS OF COVID-19
* HUNGARIAN AUTHORITIES, WHERE APPLICATION WAS MADE IN MAY,
ALSO
REFUSED AUTHORIZATION
* REFUSALS ARE MOTIVATED BY LACK OF DATA ON PHARMACOKINETICS
* DECIDED TO REPOSITION ITS COVID-19 CLINICAL DEVELOPMENT
PROGRAMME ON NON-EU COUNTRIES
Source text for Eikon: ID:nNDL28lR6p
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