drugset / Trial / NCT03776175

A Study To Assess Pharmacodynamics, Safety And Tolerability Of PF-05221304 And PF-06865571 Co-Administered For 6 Weeks In Adults With Non-Alcoholic Fatty Liver Disease.

NCT03776175

Phase 2 Completed 99 enrolled Pfizer
RandomizedParallel-groupTriple-blindTreatment

Summary

This study is to assess the effect of PF 05221304 alone, PF 06865571 alone, the co administration of PF 05221304 and PF 06865571, or placebo on whole liver fat in subjects with NAFLD. In addition, this study will evaluate the safety and tolerability of co administration of PF 05221304 and PF 06865571 along with the effects on selected pharmacodynamics (PD)/exploratory parameters, compared to administration of PF 05221304 alone, PF 06865571 alone, and placebo in adults with NAFLD.

Timeline

Start
2019-01-04
Primary completion
2019-09-09
Completion
2019-10-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Clesacostat Small molecule 15 mg Oral
Subject PF-06865571 Small molecule 300 mg Oral

Indications