NDA for Potential Progressive Familial Intrahepatic Cholestasis Treatment Cleared by FDA
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NDA for Potential Progressive Familial Intrahepatic Cholestasis Treatment Cleared by FDA

According to a press release from the rare liver disease company Albireo Pharma, Inc., the US Food and Drug Administration (FDA) has accepted its New Drug Application (NDA) for odevixibat.…

Continue Reading NDA for Potential Progressive Familial Intrahepatic Cholestasis Treatment Cleared by FDA
Experimental Treatment for Biliary Atresia Gets Orphan Drug Designation in the EU
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Experimental Treatment for Biliary Atresia Gets Orphan Drug Designation in the EU

According to a story from Market Screener, the drug developer Albireo Pharma, Inc., recently announced that its investigational product candidate A4250 has earned Orphan Drug designation from the European Commission.…

Continue Reading Experimental Treatment for Biliary Atresia Gets Orphan Drug Designation in the EU