Clinical Trials Directory

Trials / Terminated

TerminatedNCT00787137

Single Dose PG102 in Patients With Active Psoriatic Arthritis

A Randomised, Double Blind, Placebo Controlled, Single Ascending Dose, Phase I Study To Evaluate The Safety, Tolerability And Pharmacokinetics Of PG102 (Anti-CD40 Monoclonal Antibody) In Patients With Active Psoriatic Arthritis

Status
Terminated
Phase
Phase 1
Study type
Interventional
Enrollment
17 (actual)
Sponsor
PanGenetics UK Limited · Industry
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

The primary objective is to evaluate the safety and tolerability of a single intravenous dose of PG102 in patients with psoriatic arthritis. The secondary objectives are to evaluate how PG102 moves around the body and to explore its effects on the disease.

Conditions

Interventions

TypeNameDescription
DRUGPG102A single intravenous infusion
DRUGPlacebo comparatorPhosphate-buffered saline

Timeline

Start date
2008-12-01
Primary completion
2010-04-01
Completion
2010-05-01
First posted
2008-11-07
Last updated
2010-10-26
Results posted
2010-10-15

Locations

1 site across 1 country: Serbia

Source: ClinicalTrials.gov record NCT00787137. Inclusion in this directory is not an endorsement.

Single Dose PG102 in Patients With Active Psoriatic Arthritis (NCT00787137) · Clinical Trials Directory