A Placebo-controlled Safety and Tolerability Study of Intravenous (IV) and Subcutaneous (SC) AZD1163 in Healthy Volunteers

PHASE1Active, not recruitingINTERVENTIONAL
Enrollment

140

Participants

Timeline

Start Date

November 1, 2023

Primary Completion Date

January 13, 2026

Study Completion Date

January 13, 2026

Conditions
Healthy Volunteers
Interventions
BIOLOGICAL

AZD1163

"In Part 1, Participants will receive AZD1163 through IV infusion or SC injection on Day 1.~In Part 2, participants will receive AZD1163 through SC injection on Days 1 and 15."

OTHER

Placebo

"In Part 1, Participants will receive matching placebo through IV infusion or SC injection on Day 1.~In Part 2, participants will receive matching placebo through SC injection on Days 1 and 15."

Trial Locations (3)

14050

Research Site, Berlin

21225

Research Site, Brooklyn

91206

Research Site, Glendale

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Parexel

INDUSTRY

lead

AstraZeneca

INDUSTRY