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Assessment of Grazax® Treatment Compliance

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00293046
First Posted: February 17, 2006
Last Update Posted: September 30, 2008
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
ALK-Abelló A/S
February 16, 2006
February 17, 2006
September 30, 2008
February 2006
September 2006   (Final data collection date for primary outcome measure)
Assessment of treatment compliance by recording of drug accountability
Same as current
Complete list of historical versions of study NCT00293046 on ClinicalTrials.gov Archive Site
Recording of adverse events
Same as current
Not Provided
Not Provided
 
Assessment of Grazax® Treatment Compliance
A Randomised, Parallel-Group, Open, Controlled Phase III Trial Assessing the Treatment Compliance With GRAZAX® in Subjects With Seasonal Grass Pollen Induced Rhinoconjunctivitis
This trial is performed to assess whether the Grazax® treatment compliance can be improved by use of a compliance device (Memozax®).
Not Provided
Interventional
Phase 3
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Allergy
Biological: ALK Grass tablet - use of compliance device
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
500
October 2007
September 2006   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Grass pollen induced rhinoconjunctivitis
  • Males and females, 18-65 years of age
  • Positive skin prick test

Exclusion Criteria:

  • Previous treatment with grass pollen allergen
Sexes Eligible for Study: All
18 Years to 65 Years   (Adult)
No
Contact information is only displayed when the study is recruiting subjects
Austria
 
 
NCT00293046
GT-10
Not Provided
Not Provided
Not Provided
Not Provided
ALK-Abelló A/S
Not Provided
Study Director: Kim Simonsen, MD ALK-Abelló A/S
ALK-Abelló A/S
September 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP