drugset / Trial / NCT04155645

To Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AZD8233 After Multiple Dose Administration in Subjects With Dyslipidemia

NCT04155645 ↗

Phase 1 Completed 34 enrolled AstraZeneca Parexel · collab
RandomizedParallel-groupSingle-blindTreatment

Summary

This is a Phase I study to assess the safety, tolerability and pharmacokinetics (PK), and pharmacodynamics (PD) of AZD8233, following subcutaneous (SC) administration of multiple ascending doses (MAD) of AZD8233 in subjects with confirmed dyslipidemia with or without type 2 diabetes.

Timeline

Start
2019-11-21
Primary completion
2021-06-07
Completion
2021-06-07

Drugs

EvaluationDrugModalityDoseRoute
Subject AZD8233 Antisense oligonucleotide — Subcutaneous

Indications