RESPONSE: Response to Seladelpar in Subjects With Primary Biliary Cholangitis (PBC) and an Inadequate Control to or an Intolerance to Ursodeoxycholic Acid (UDCA)
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- STATUS
- Recruiting
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- End date
- Mar 8, 2023
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- participants needed
- 180
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- sponsor
- CymaBay Therapeutics, Inc.
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 Identifier | NCT04620733 |
| Sponsor | CymaBay Therapeutics, Inc. |
| Last Modified on | 8 August 2022 |
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