Clinical Trials Directory

Trials / Completed

CompletedNCT02603224

Safety, Tolerability and Pharmacokinetic Study of MRG-201 in Healthy Volunteers

A Phase 1, Double-Blind, Placebo-Controlled, Single and Multiple Dose-Escalation Study to Investigate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamic Activity of MRG-201 Following Local Intradermal Injection in Normal Healthy Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
54 (actual)
Sponsor
miRagen Therapeutics, Inc. · Industry
Sex
Male
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The primary objective of this study is to evaluate the safety and tolerability of the investigational drug, MRG-201, in healthy volunteers. MRG-201 is designed to mimic the activity of a molecule called miR-29 that decreases the expression of collagen and other proteins that are involved in scar formation. MRG-201 is being studied to determine if it can limit the formation of fibrous scar tissue in certain diseases. MRG-201 will be tested in healthy volunteers by injection into intact skin or adjacent to a short skin incision. Volunteers may receive one or several doses of MRG-201, and will be monitored for local reactions in the skin, signs or symptoms of adverse effects on the body, and for the levels of MRG-201 in the blood over time. Skin biopsies will also be collected to study how cells in the skin respond when exposed to MRG-201.

Detailed description

Study Design: Cohorts of 3-6 healthy male volunteers, ages 18-45, will receive single or multiple ascending doses of MRG-201 by intradermal injection at one site and placebo at a second site over a period of up to 15 days, with follow-up for up to 28 days after the last dose to determine the maximum tolerated dose in intact or incised normal skin and the tendency for active drug to diffuse through the skin.

Conditions

Interventions

TypeNameDescription
DRUGMRG-201Intradermal injection of single ascending doses and multiple ascending doses in healthy volunteers.
DRUGPlaceboIntradermal injection of placebo at a second site in healthy volunteers. Each subject will serve as their own control.

Timeline

Start date
2015-11-01
Primary completion
2017-04-01
Completion
2017-04-01
First posted
2015-11-11
Last updated
2017-07-06

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT02603224. Inclusion in this directory is not an endorsement.