Efficacy and Safety of a Purified Standardised Wasp Venom Preparation

The trial is performed to assess efficacy and safety of a purified standardised wasp venom preparation in wasp venom allergy

Completed

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Key information

Conditions

Allergy Hypersensitivity Hypersensitivity, Immediate Immune System Diseases Venom Hypersensitivity

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Allergopharma GmbH & Co. KG

Reinbek, 21465, Germany

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

History of wasp venom allergy,
Positive RAST to wasp venom,
Positive skin prick test to wasp venom

Exclusion criteria

Serious chronic diseases

Treatment and study plan

wasp venom

Biological

Sponsors and collaborators

Lead sponsor

Allergopharma GmbH & Co. KG

Industry

Registry information

Official study title

Immunotherapy of Wasp Venom Allergy: Comparison of a Purified Preparation to Conventional Aqueous Wasp Venom in an Open Controlled Study

Important dates

Study start: 2001
Primary completion: 2007
Study completion: 2010
First posted: Dec 12, 2005
Registry last updated: Mar 11, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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