RESPONSE: Response to Seladelpar in Subjects With Primary Biliary Cholangitis (PBC) and an Inadequate Control to or an Intolerance to Ursodeoxycholic Acid (UDCA)

  • STATUS
    Not Recruiting
  • End date
    Mar 8, 2023
  • participants needed
    180
  • sponsor
    CymaBay Therapeutics, Inc.
Updated on 14 September 2022
Investigator
Elaine Watkins, DO, MSPH
Primary Contact
Toronto Digestive Disease Associates Inc (9.6 mi away) Contact
+157 other location

Summary

To evaluate the treatment effect of seladelpar on composite biochemical improvement in cholestasis markers based on ALP and total bilirubin and to evaluate the safety of seladelpar over 12 months of treatment compared to placebo

Details
Condition Primary Biliary Cholangitis
Treatment Placebo, seladelpar 10 mg, Seladelpar 5 mg
Clinical Study IdentifierNCT04620733
SponsorCymaBay Therapeutics, Inc.
Last Modified on14 September 2022

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