drugset / Trial / NCT04269031

A First-in-human Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AZD2373 After Single Dose Administration in Healthy Male Subjects of African Ancestry.

NCT04269031 ↗

Phase 1 Completed 30 enrolled AstraZeneca Parexel · collab
RandomizedSequentialDouble-blindTreatment

Summary

This is a Phase 1 study to assess the the safety, tolerability and pharmacokinetics (PK) of AZD2373, following subcutaneous (SC) administration of single ascending doses (SAD) of AZD2373 in healthy male subjects of African ancestry.

Timeline

Start
2020-02-13
Primary completion
2021-08-31
Completion
2021-08-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Opemalirsen Unknown — Subcutaneous

Indications

No indication recorded.