Phase 2b Study of NGM282 Extended Treatment in Patients With Primary Biliary Cirrhosis



Status:Completed
Conditions:Gastrointestinal
Therapuetic Areas:Gastroenterology
Healthy:No
Age Range:18 - 75
Updated:3/29/2017
Start Date:May 2014
End Date:February 2016

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A Phase 2, Multi-Center Study to Evaluate Three Doses of NGM282 Administered for 24 Weeks in Patients With Primary Biliary Cirrhosis (PBC) Who Have Completed Study 13-0103

The purpose of this study is to determine the safety, tolerability, and activity of extended
treatment with NGM282 in patients with Primary Biliary Cirrhosis.


Inclusion Criteria:

- Completion of NGM 13-0103

- Males or females, between 18 and 75 years of age, inclusive

- PBC Diagnosis consistent with AASLD and EASL guidelines

- Stable dose of UDCA

Exclusion Criteria:

- Chronic liver disease of a non-PBC etiology

- Evidence of clinically significant hepatic decompensation
We found this trial at
7
sites
Sydney, New South Wales
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Sydney,
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Coronado, California
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Coronado, CA
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Dallas, TX
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Detroit, Michigan
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Detroit, MI
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Durham, North Carolina
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Durham, NC
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Phoenix, Arizona
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Phoenix, AZ
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San Antonia, Texas
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San Antonia, TX
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