Safety and Efficacy of Recombinant Birch Pollen Allergen in the Treatment of Allergic Rhinoconjunctivitis

NCT ID: NCT00309062

Last Updated: 2013-03-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Study Classification

INTERVENTIONAL

Study Start Date

2003-12-31

Study Completion Date

2009-06-30

Brief Summary

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Safety and efficacy of recombinant birch pollen allergen in the treatment of allergic rhinoconjunctivitis

Detailed Description

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Conditions

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Birch Pollen Allergy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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Recombinant birch pollen

Intervention Type BIOLOGICAL

Eligibility Criteria

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Inclusion Criteria

* Positive Skin Prick Test reaction to birch pollen
* Positive RAST result to birch pollen
* Positive Provocation Test result to birch pollen

Exclusion Criteria

* Serious chronic diseases
* Other perennial allergies
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Allergopharma GmbH & Co. KG

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Annemie Narkus, M D

Role: PRINCIPAL_INVESTIGATOR

Locations

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Allergopharma GmbH & Co. KG

Reinbek, , Germany

Site Status

Countries

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Germany

Related Links

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http://www.allergopharma.de

Leader in specific allergy research and therapy

Other Identifiers

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Al0103rB

Identifier Type: -

Identifier Source: org_study_id

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