A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED PHASE 2 STUDY TO EVALUATE EFFICACY AND SAFETY OF CP-945,598 IN SUBJECTS WITH NON-ALCOHOLIC STEATOHEPATITIS

Update Il y a 4 ans
Reference: EUCTR2008-004088-21

Woman and Man

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Extract

To evaluate the efficacy of 20 mg QD and 5 mg QD of CP-945,598 given for 48 weeks in the treatment of NASH.


Inclusion criteria

  • Non- alcoholic steatohepatitis

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