drugset / Trial / NCT02784444

A Study to Evaluate the Safety, Tolerability & Efficacy of MSDC-0602K in Patients With NASH

NCT02784444 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a randomized, double-blinded study of three doses of MSDC-0602K or placebo given orally once daily to subjects with biopsy proven NASH with fibrosis and no cirrhosis.

Timeline

Start
2016-09-14
Primary completion
2019-06
Completion
2019-06

Drugs

EvaluationDrugModalityDoseRoute
Comparator MSDC-0602K Unknown 62.5 mg Oral
Comparator MSDC-0602K Unknown 125 mg Oral
Comparator MSDC-0602K Unknown 250 mg Oral