drugset / Trial / NCT01926366

AZD6423 SAD/MAD Study in Healthy Volunteers

NCT01926366 ↗

Phase 1 Completed 175 enrolled AstraZeneca
RandomizedParallel-groupDouble-blindBasic science

Summary

This is a randomized, double-blind, placebo-controlled study of single and multiple ascending dosage levels of AZD6423 in healthy volunteers. The study includes an up to 28-day screening period, an in-house period during which AZD6423 or placebo will be administered IV, and a 4- to 10-day follow-up period after discharge.

Timeline

Start
2013-09
Primary completion
2014-03
Completion
2014-03

Drugs

EvaluationDrugModalityDoseRoute
Subject AZD6423 Unknown — Intravenous

Indications

No indication recorded.