Clinical Trials Directory

Trials / Completed

CompletedNCT00941746

Safety and Tolerability of PG110 in Patients With Knee Osteoarthritis Pain

A Randomised, Double-blind, Placebo-controlled, Single Ascending Dose, Phase I Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of PG110 (Anti-NGF Monoclonal Antibody) in Patients With Pain Attributed to Osteoarthritis of the Knee

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
56 (actual)
Sponsor
Abbott · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the safety and tolerability of a single intravenous dose of PG110, a monoclonal antibody that inhibits the effects of the naturally occurring substance, nerve growth factor (NGF).

Conditions

Interventions

TypeNameDescription
BIOLOGICALPG110Single, slow intravenous infusion
BIOLOGICALPG110Single, slow intravenous infusion
BIOLOGICALPG110Single, slow intravenous infusion
BIOLOGICALPG110Single, slow intravenous infusion
BIOLOGICALPG110Single, slow intravenous infusion
BIOLOGICALPG110Single, slow intravenous infusion
BIOLOGICALPG110Single, slow intravenous infusion
BIOLOGICALPG110Single, slow intravenous infusion
BIOLOGICALPlaceboSingle, slow intravenous infusion that matches PG110 in appearance

Timeline

Start date
2009-08-01
Primary completion
2011-01-01
Completion
2011-01-01
First posted
2009-07-20
Last updated
2011-06-07

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT00941746. Inclusion in this directory is not an endorsement.