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Trials / Completed

CompletedNCT01620762

Phase III Cat-PAD Study

A Double-Blind, Randomised, Placebo-Controlled Multi-Centre Field Study to Assess the Efficacy and Safety of Cat-PAD Peptide Immunotherapy in Cat Allergic Subjects

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
1,408 (actual)
Sponsor
Circassia Limited · Industry
Sex
All
Age
12 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the treatment effect of two treatment regimens of Cat-PAD vs placebo and to evaluates the treatment effect of Cat-PAD on symptoms, rescue medication usage and Quality of Life.

Conditions

Interventions

TypeNameDescription
DRUGCat-PAD1 dose every 4 weeks
DRUGPlacebo1 dose every 4 weeks

Timeline

Start date
2012-10-01
Primary completion
2016-06-01
First posted
2012-06-15
Last updated
2018-06-15
Results posted
2018-05-14

Locations

118 sites across 9 countries: United States, Belgium, Canada, Czechia, Germany, Hungary, Poland, Russia, Slovakia

Source: ClinicalTrials.gov record NCT01620762. Inclusion in this directory is not an endorsement.

Phase III Cat-PAD Study (NCT01620762) · Clinical Trials Directory