drugset / Trial / NCT04630067

Assessment of Safety, Tolerability, Immunogenicity, and Pharmacokinetics of AZD3427

NCT04630067

Phase 1 Completed 105 enrolled AstraZeneca
RandomizedParallel-groupDouble-blindTreatment

Summary

This first-time-in-human (FTIH) study will be conducted to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and immunogenicity of single doses of AZD3427 in healthy volunteers and multiple doses of AZD3427 in patients with heart failure (HF).

Timeline

Start
2020-11-17
Primary completion
2022-09-14
Completion
2022-09-14

Drugs

EvaluationDrugModalityDoseRoute
Subject AZD3427 Unknown 5 mg Subcutaneous
Subject AZD3427 Unknown 10 mg Subcutaneous
Subject AZD3427 Unknown 15 mg Subcutaneous
Subject AZD3427 Unknown 30 mg Subcutaneous
Subject AZD3427 Unknown 45 mg Subcutaneous
Subject AZD3427 Unknown 90 mg Subcutaneous
Subject AZD3427 Unknown 270 mg Subcutaneous

Indications