A Study to Assess the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics of Subcutaneous AZD6912 in Healthy Participants

PHASE1Active, not recruitingINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

November 15, 2023

Primary Completion Date

March 30, 2026

Study Completion Date

March 30, 2026

Conditions
Rheumatoid Arthritis
Interventions
DRUG

AZD6912

AZD6912 will be administered as a single sub-cutaneous dose.

DRUG

Placebo

Placebo will be administered as a single sub-cutaneous dose.

Trial Locations (2)

H3P 3P1

Research Site, Montreal

HA1 3UJ

Research Site, Harrow

Sponsors

Lead Sponsor

All Listed Sponsors
lead

AstraZeneca

INDUSTRY