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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00309036
Other study ID # Al0403rP
Secondary ID
Status Completed
Phase Phase 3
First received March 30, 2006
Last updated March 8, 2013
Start date January 2004
Est. completion date May 2008

Study information

Verified date March 2013
Source Allergopharma GmbH & Co. KG
Contact n/a
Is FDA regulated No
Health authority Germany: Paul-Ehrlich-Institut
Study type Interventional

Clinical Trial Summary

The trial is performed to assess efficacy and safety of a recombinant grass Pollen allergen cocktail in allergic rhinoconjunctivitis


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date May 2008
Est. primary completion date September 2006
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Positive Skin Prick Test reaction to grass pollen

- Positive RAST result to grass pollen

- Positive Provocation Test result to grass pollen

Exclusion Criteria:

- Serious chronic diseases

- Other relevant perennial allergies

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Biological:
Recombinant grass pollen


Locations

Country Name City State
Germany Allergopharma GmbH & Co. KG Reinbek

Sponsors (1)

Lead Sponsor Collaborator
Allergopharma GmbH & Co. KG

Country where clinical trial is conducted

Germany, 

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