COPENHAGEN, NOVEMBER 01 2017 – AntibioTx, a clinical stage, pharmaceutical company targeting antimicrobial infections and microbiome-related disorders today announced that the U.S Food and Drug Administration (FDA) has granted an Investigational New Drug (IND) approval of AntibioTx’s ATx201 for treatment of microbiome related skin disorders.
“The FDA approval of our IND is very well-timed since we are ready to initiate studies in North America” said Dr. Lutz Wevelsiep VP of Drug Regulatory Affairs of AntibioTx” The approval to conduct studies in the US has been a key prioritization for a long time and therefore this is a fundamental milestone for AntibioTx”.
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