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An Open Label Single Arm Study to Investigate the Safety and Efficacy of Multiple Administrations of NI-0801, a Fully Human Anti-CXCL10 Monoclonal Antibody in PBC Patients With an Incomplete Response to Ursodeoxycholic Acid (PIANO)

NCT01430429 Phase 2 TERMINATED

The purpose of the study is to assess safety and efficacy of multiple doses of NI-0801 in primary biliary cirrhosis patients with an inadequate response to ursodeoxycholic acid.

Details

Lead sponsorLight Chain Bioscience - Novimmune SA
PhasePhase 2
StatusTERMINATED

Conditions

Interventions

Countries

Italy, United Kingdom