Efficacy and Safety Trial of Pangramin SLIT HDM-mix in Subjects With House Dust Mite Induced Rhinitis

ALK-Abelló

Status and phase

Completed

Phase 3

Conditions

Allergic Rhinitis

Treatments

Biological: Placebo

Biological: Pangramin SLIT HDM mix.

Study type

Interventional

Funder types

Industry

Identifiers

NCT01603056

PS-M-01

Details and patient eligibility

About

Primary aim is to evaluate the efficacy of specific immunotherapy with Pangramin SLIT HDM-mix compared to placebo in the treatment of House Dust Mite (HDM) induced rhinitis with or without asthma.

Sublingual immunotherapy has been used during several years and has been shown to provide benefits compare to traditional subcutaneous treatment. This study will investigate if improvements in rhinitis symptoms and less use of symptomatic medication can be obtained as a consequence of being treated under specific immunotherapy.

This study aim also to contribute to the documentation of tolerability and safety profile of Pangramin HDM Mix.

Full description

Extensive clinical experience has been gained due to the widespread use of Pangramin® SLIT and other SLIT products as named patient products, both with respect to the types and the frequencies of the adverse events(AEs) observed. No safety concerns have been found.

The optimal therapeutic dose range regarding SLIT is not fully elucidated. The fate of the allergen after sublingual administration is not known in detail, i.e. to what extent is the allergen absorbed over the mucosa or swallowed and how this is related to volume, excipients etc. The relationship between dose and effect is thus not fully elucidated. The general recommendation is to use a dose inducing a clinical relevant effect in most patients without causing unacceptable adverse events. As Pangramin SLIT HDM-mix has a safety profile that allows a single daily intake by the patient at home, the dosage at this trial will be the same as marketed product.

Enrollment

617 patients

Sex

All

Ages

5 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Male or female ≥ 5 to ≤ 55 years of age.
A history HDM induced allergic rhinitis.
Use of medication for the control of rhinoconjunctivitis symptoms.
Positive Skin Prick Test (SPT).
Positive specific IgE.

Exclusion criteria

PEF ≤ 70% of predicted value.
History of significant symptomatic seasonal or perennial allergic rhinitis and/or asthma caused by an allergen to which the patient is regularly exposed, and sensitized (e.g. pollens, cat, dog, cockroach...except house dust mites).
Severe asthma.
Current symptoms of upper respiratory tract infection or other relevant infectious process.
Current food allergies with oral allergy syndrome.
A clinical history of chronic sinusitis.
Current severe atopic dermatitis.
Concomitant or previous treatment by immunotherapy.