Clinical Trials Directory

Trials / Completed

CompletedNCT01813084

A Study to Investigate the Safety, Tolerability and Pharmacokinetics of Single and Repeat Doses of RV1729

A Randomised, Double Blind, Placebo-controlled, Three Part Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Treatment With Single and Repeat Doses of Inhaled RV1729 in Healthy Subjects and Subjects With Mild to Moderate Asthma

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
63 (actual)
Sponsor
Respivert Ltd · Industry
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

RV1729 is a new medicine being developed for possible treatment of asthma and smoking related lung disease (also known as chronic obstructive pulmonary disease - COPD). The main purpose of this study is to investigate the safety, tolerability and pharmacokinetics of single and repeat doses of RV1729.

Conditions

Interventions

TypeNameDescription
DRUGRV1729 single doseSafety and tolerability of single escalating doses
DRUGRV1729 matching placebo single doseSafety and tolerability of single escalating doses
DRUGRV1729: 14 day repeat doseSafety and tolerability of repeat escalating doses
DRUGRV1729 matching placebo: 14 day repeat doseSafety and tolerability of repeat escalating doses

Timeline

Start date
2013-05-01
Primary completion
2014-04-01
Completion
2014-04-01
First posted
2013-03-18
Last updated
2014-04-24

Locations

2 sites across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT01813084. Inclusion in this directory is not an endorsement.