drugset / Trial / NCT06995820

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

NCT06995820 ↗

Phase 1 Recruiting 136 enrolled AstraZeneca Parexel · collab
RandomizedSequentialSingle-blindTreatment

Summary

The purpose of the study is to assess the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and immunogenicity of AZD1613 in healthy participants, including Japanese and Chinese descent.

Timeline

Start
2025-06-06
Primary completion
2026-09-23
Completion
2026-09-23

Drugs

EvaluationDrugModalityDoseRoute
Subject AZD1613 Unknown — Subcutaneous

Indications

No indication recorded.