Stroke Clinical Trial
Official title:
A Phase 1, Double-Blind, Randomized, Placebo-Controlled, Sequential-Group Study to Assess the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Ascending Doses of AER-271 in Healthy Subjects
The objective of this Phase 1 trial is to assess the safety, tolerability and pharmacokinetics of AER-271 in health subjects.
This is a double-blind, randomized, placebo-controlled, sequential-group study to assess the
safety, tolerability and pharmacokinetics of single ascending dose and multiple ascending
doses of intravenously (IV) administered AER-271 in healthy human subjects. AER-271 is an
Aquaporin-4 inhibitor designed to prevent brain swelling in severe ischemic stroke. The study
will be conducted in 2 parts: Part A is a single ascending dose, sequential group study. The
subsequent Part B is a multiple ascending dose, sequential group study. Both Parts A and B
will follow an adaptive design including the use of Sentinel Dosing.
The primary objectives of this study are to assess the safety and tolerability of single and
multiple IV doses and continuous infusion of AER-271 in healthy subjects. Secondary
objectives include: determining the pharmacokinetics of AER-271 and AER-270 following
administration of AER-271, determining the dose proportionality for AER-270 and 271, and
comparing the effects of continuous infusion versus multiple bolus doses on AER-271 exposure
and adverse events. An additional exploratory objective of this study is to evaluate the
effects of AER-271 on electrocardiogram parameters including QT interval corrected for heart
rate. Data from this trial will also be used to develop a protocol for a subsequent Phase 2
clinical trial in stroke patients.
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