Clinical Trials Directory

Trials / Completed

CompletedNCT01355016

A Trial to Assess the Safety, Tolerability, and Pharmacokinetics of MDT-637 in Healthy Volunteers

A Randomized, Double-blind, Placebo-controlled, Single Ascending Dose Study to Assess the Safety, Tolerability and Pharmacokinetics of Inhaled MDT-637 in Healthy Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
48 (estimated)
Sponsor
MicroDose Therapeutx, Inc · Industry
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to determine the range of single inhaled doses of a new dry powder product, MDT-637, that are safe and well-tolerated. This includes monitoring effects on pulmonary function and determination of blood levels of MDT-637 following inhalation.

Conditions

Interventions

TypeNameDescription
DRUGMDT-637Inhaled doses of MDT-637 over a 24 hour period

Timeline

Start date
2011-09-01
Primary completion
2011-11-01
Completion
2011-11-01
First posted
2011-05-17
Last updated
2012-04-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01355016. Inclusion in this directory is not an endorsement.

A Trial to Assess the Safety, Tolerability, and Pharmacokinetics of MDT-637 in Healthy Volunteers (NCT01355016) · Clinical Trials Directory