- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00263952
Efficacy and Safety of a Purified Standardised Bee Venom Preparation
March 1, 2013 updated by: Allergopharma GmbH & Co. KG
Immunotherapy of Bee Venom Allergy: Evaluation of a New Purified Bee Venom Preparation in Comparison With Already Published Studies.
The trial is performed to assess efficacy and safety of a purified standardised bee venom preparation in bee venom allergy
Study Overview
Study Type
Interventional
Phase
- Phase 3
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Reinbek, Germany, 21465
- Allergopharma GmbH & Co. KG
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- History of bee venom allergy,
- Positive RAST for bee venom,
- Positive skin prick test for bee venom
Exclusion Criteria:
- Serious chronic diseases
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Annemie Narkus, M.D.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2003
Primary Completion (Actual)
January 1, 2005
Study Completion (Actual)
April 1, 2010
Study Registration Dates
First Submitted
December 9, 2005
First Submitted That Met QC Criteria
December 9, 2005
First Posted (Estimate)
December 12, 2005
Study Record Updates
Last Update Posted (Estimate)
March 4, 2013
Last Update Submitted That Met QC Criteria
March 1, 2013
Last Verified
March 1, 2013
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Al0202ig
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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