Clinical Trials Directory

Trials / Completed

CompletedNCT00857779

Study on Pharmacodynamic Parameter and Tolerability With Subcutaneous Immunotherapy in Grass Pollen Allergic Patients

A Multicentre Randomised Phase II Clinical Trial to Demonstrate Equivalent Pharmacodynamic Efficacy and Tolerability of Two Updosing Schedules for ALK-Flex SQ

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
473 (actual)
Sponsor
ALK-Abelló A/S · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to test the pharmacodynamic equivalence with respect to IgE-blocking factor and to compare the tolerability of two different updosing schedules with ALK-Flex SQ

Conditions

Interventions

TypeNameDescription
BIOLOGICALsubcutaneous immunotherapy7 injections

Timeline

Start date
2009-02-01
Primary completion
2009-08-01
Completion
2009-10-01
First posted
2009-03-09
Last updated
2013-02-08

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT00857779. Inclusion in this directory is not an endorsement.

Study on Pharmacodynamic Parameter and Tolerability With Subcutaneous Immunotherapy in Grass Pollen Allergic Patients (NCT00857779) · Clinical Trials Directory