A Study to Assess the Safety, Tolerability, and Pharmacokinetics of AZD9550 Following Single Ascending Dose Administration to Healthy Participants

PHASE1CompletedINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

May 2, 2023

Primary Completion Date

November 13, 2023

Study Completion Date

November 13, 2023

Conditions
Non-alcoholic Steatohepatitis
Interventions
DRUG

AZD9550

Participants will be administered AZD9550 subcutaneously.

DRUG

AZD9550

Participants will be administered AZD9550 intravenously.

DRUG

Placebo

Participants will be administered matching volumes of placebo subcutaneously or intravenously.

Trial Locations (1)

HA1 3UJ

Research Site, Harrow

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Parexel

INDUSTRY

lead

AstraZeneca

INDUSTRY