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Gannex Announces First Subject Dosed in the U.S. Drug-Drug Interaction Study of FXR Agonist ASC42 for Treatment of Primary Biliary Cholangitis - Press Release

Enrollment of the total 12 subjects is expected to be completed in August 2022 The DDI study on ASC42 in the U.S. is expected to be completed by ....

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Gannex Announces First Subject Dosed in the U.S. Drug-Drug Interaction Study of FXR Agonist ASC42 for Treatment of Primary Biliary Cholangitis

/PRNewswire/ Gannex Pharma Co., Ltd. ("Gannex"), a wholly owned company of Ascletis Pharma Inc. (HKEX: 1672) today announces that it has completed the first. ....

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Gannex Announces U.S. FDA Clearance of Clinical Trial on FXR Agonist ASC42 for Treatment of Primary Biliary Cholangitis

ASC42 has completed Phase I trials in the U.S. and China. This approval from U.S. FDA enables Gannex to complete a critical drug-drug interaction (DDI) study to support upcoming Phase III trials in China, the U.S. and European Union Gannex expects to complete this DDI study at the beginning of Q4, 2022 Currently, Phase II clinical trial of FXR agonist ASC 42 in China is in progress. Gannex intends to start Phase III clinical trials in China, the U.S. and European Union after the completion of the Phase II clinical trial which is ongoing in China SHANGHAI, June 8, 2022 /PRNewswire/ Gannex, a wholly owned company of Ascletis Pharma Inc. (HKEX: 1672) today announces that it has obtained the U.S. FDA clearance for itsdrug candidate, ASC42, to initiate a drug-drug interaction (DDI) study. This important DDI study is designed to provide more evidence to support upcoming Phase III clinical trials in China, the U.S. and European Union for treatment of primary biliary cholangitis (PBC). ....

United States , Hong Kong , Clin Gastroenterol Hepatol , Jinzij Wu , Prnewswire Gannex , Hong Kong Stock Exchange , European Union , Ascletis Pharma Inc , Ascletis Pharma , Obeticholic Acid , Primary Biliary Cholangitis , Reduced Mortality With Treatment , Biliary Cholangitis , American Association , Liver Diseases , Sc42 Has Completed Phasei Trials In The Us And China This Approval From Fda Enables Gannex To Completea Critical Drug Interaction Ddi Study Support Upcoming Phase Iii , He Us And European Union Gannex Expects To Complete This Ddi Study At The Beginning Of Q4 , 022 Currently , Hase Ii Clinical Trial Of Fxr Agonist Asc 42 In China Is Progress Gannex Intends To Start Phase Iii Trials , He Us And European Union After The Completion Of Phase Ii Clinical Trial Which Is Ongoing In China Shanghai , June 8 , 022 Prnewswire Gannex , A Wholly Owned Company Of Ascletis Pharma Inc Hkex 1672 Today Announces That It Has Obtained The Us Fda Clearance For Itsdrug Candidate , O Initiatea Drug Interaction Ddi Study This Important Is Designed To Provide More Evidence Support Upcoming Phase Iii Clinical Trials In China , He Us And European Union For Treatment Of Primary Biliary Cholangitis Pbc Asc42 Is An In House Developed , Ovel Non Steroidal ,

Gannex Announces U.S. FDA Clearance of Clinical Trial on FXR Agonist ASC42 for Treatment of Primary Biliary Cholangitis

ASC42 has completed Phase I trials in the U.S. and China. This approval from U.S. FDA enables Gannex to complete a critical drug-drug interaction (DDI). ....

United States , Hong Kong , Clin Gastroenterol Hepatol , Jinzij Wu , Prnewswire Gannex , Hong Kong Stock Exchange , European Union , Ascletis Pharma Inc , Ascletis Pharma , Obeticholic Acid , Primary Biliary Cholangitis , Reduced Mortality With Treatment , Biliary Cholangitis , American Association , Liver Diseases , Ascletis Pharma Inc , Medical Pharmaceuticals , Health Care Amp Hospitals , International Medical Approval ,

Gannex Announces First Patient Dosed in Phase II Clinical Trial of ASC42, an FXR Agonist, for Primary Biliary Cholangitis

/PRNewswire/ Gannex Pharma Co., Ltd. ("Gannex"), a wholly owned company of Ascletis Pharma Inc. (HKEX:1672) announces today the first patient dosed in the. ....

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