A Study of AZD1613 in Healthy Participants

This study is looking for healthy volunteers, aged 18 to 50, to test a new drug called AZD1613. The main goal is to understand if AZD1613 is safe and how well your body tolerates it. Researchers will also study how the drug moves through your body (pharmacokinetics), what effects it has on your body (pharmacodynamics), and if your immune system reacts to it (immunogenicity). You would receive either AZD1613 or a placebo (an inactive substance) as an injection under the skin or into a vein. The study is currently unclear on its recruitment status.

Study design
This is a randomized, single-blind, placebo-controlled study with up to 136 healthy participants. It has two parts: Part A for a single dose and Part B for multiple doses.
What's involved
You would have a screening period of up to 28 days, receive the study drug or placebo on specific days, and then have follow-up visits for up to 161 days.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for adverse events for up to 161 days after the first dose.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06995820

A Study to Investigate Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Immunogenicity of AZD1613 in Healthy Participants.

Recruiting
PHASE1Ages 18–50InterventionalTreatment
AstraZeneca
~136 participants
Updated 2026-05-15 on ClinicalTrials.gov
What's tested:AZD1613Placebo

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Number of participants with adverse events (AEs) and serious AEs.
Measured over AEs: Part A: From Day 1 to Final Follow-up (Day 105); Part B: From Day 1 to Final Follow-up (Day 161); SAEs: Part A: From Screening (Day -28 to Day -2) to Final Follow-up visit (Day 105) Part B: From Screening (Day -28) to Final Follow-up visit (Day 161)
Healthy
1 sites across 1 states
California1
AstraZeneca Clinical Study Information Center
Email the study team

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  • Number of participants with adverse events (AEs) and serious AEs.AEs: Part A: From Day 1 to Final Follow-up (Day 105); Part B: From Day 1 to Final Follow-up (Day 161); SAEs: Part A: From Screening (Day -28 to Day -2) to Final Follow-up visit (Day 105) Part B: From Screening (Day -28) to Final Follow-up visit (Day 161)

    To assess the safety and tolerability of AZD1613 following SC and/or IV administration of single and multiple ascending doses.