Last updated on January 2019

AURORA: Phase 3 Study for the Efficacy and Safety of CVC for the Treatment of Liver Fibrosis in Adults With NASH

Brief description of study

The AURORA study will be conducted to confirm the efficacy and safety of cenicriviroc (CVC) for the treatment of liver fibrosis in adult subjects with NASH.

Detailed Study Description

The AURORA study will be conducted in 2 parts. Part 1 will examine the surrogate endpoint of improvement in fibrosis of at least 1 stage (nonalcoholic steatohepatitis clinical research network [NASH CRN]) and no worsening of steatohepatitis at Month 12. Subjects from Part 1 will continue into Part 2 and additional subjects will be newly randomized in Part 2 to determine long-term clinical outcomes composed of histopathologic progression to cirrhosis, liver-related clinical outcomes, and all-cause mortality.

Clinical Study Identifier: NCT03028740

Contact Investigators or Research Sites near you

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Clinical Trials Registry Team

Hospital Nacional Edgardo Rebagliati Martins
Lima, Peru
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Clinical Trials Registry Team

Hospital Nacional Guillermo Almenara Irigoyen
La Victoria, Peru
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Clinical Trials Registry Team

SANNA - Cl nica San Borja
Distrito De Lima, Peru
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Clinical Trials Registry Team

Cl nica Delgado
Miraflores, Peru
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Clinical Trials Registry Team

Hospital Nacional Arzobispo Loayza
Cercado De Lima, Peru
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Recruitment Status: Open

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