A Study to Assess the Safety and Tolerability of Single Doses of AZD4076 in Healthy Male Subjects

PHASE1Active, not recruitingINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

November 24, 2015

Primary Completion Date

November 4, 2017

Study Completion Date

August 29, 2025

Conditions
Non-alcoholic Steatohepatitis (NASH)
Interventions
DRUG

AZD4076

Subcutaneous (SC) administration of single ascending doses; there will be no more than 2 mL per syringe/injection

DRUG

Placebo

Subcutaneous (SC) administration of single ascending doses; there will be no more than 2 mL per syringe/injection

Trial Locations (1)

21225

Research Site, Brooklyn

Sponsors

Lead Sponsor

All Listed Sponsors
lead

AstraZeneca

INDUSTRY