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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00263952
Other study ID # Al0202ig
Secondary ID
Status Completed
Phase Phase 3
First received December 9, 2005
Last updated March 1, 2013
Start date March 2003
Est. completion date April 2010

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 purified standardised bee venom preparation in bee venom allergy


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date April 2010
Est. primary completion date January 2005
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility 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 Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Biological:
bee venom


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, 

See also
  Status Clinical Trial Phase
Recruiting NCT04259359 - Predominant Sensitizations to Single Bee Venom Allergens as a Risk Factor for Therapy Failure
Completed NCT04435678 - Diagnostic Accuracy of the MADx Multi Array Xplorer (MAX 45k) Automated Laboratory System and the MADx Allergy Explorer Version 2 (ALEX²) - IgE Multiplex Test for the Diagnosis of Pre-defined Groups of Specific High-priority Allergens N/A