A Study of NPT189 in Healthy Subjects

Status Completed

Clinical Trial Summary

The purpose of the study is to evaluate the safety and tolerability of single dose of NPT189 in healthy volunteers. The study will also evaluate the pharmacokinetic characteristics of NPT189.

Clinical Trial Description

This study is a Phase1, randomized, double-blind, placebo-controlled, single dose, dose escalation safety and tolerability study of NPT189 in health subjects. Six dose cohorts are planned each with a maximum of 8 participants per cohort. Participants will receive NPT189 by intravenous (IV) or a matching placebo by intravenous infusion. Safety, tolerability, and pharmacokinetics will be assessed. ;

Study Design

Related Conditions & MeSH terms

Amyloidosis

Clinical Trial Details

NCT number	NCT03610035
Study type	Interventional
Source	Proclara Biosciences, Inc.
Contact
Status	Completed
Phase	Phase 1
Start date	July 24, 2018
Completion date	February 17, 2019

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