A placebo controlled study to assess after two years of treatment the efficacy and safety of a birch pollen extract solution at a dose of 300IR taken under the tongue and once daily by patients with birch pollen related rhinoconjunctivitis.

• Conditions: Birch pollen allergic Rhinoconjunctivitis; MedDRA version: 14.0Level: LLTClassification code 10066093Term: Birch pollen allergySystem Organ Class: 10021428 - Immune system disorders; Therapeutic area: Body processes [G] - Immune system processes [G12]

• Registration Number: EUCTR2010-020693-42-SE
• Lead Sponsor: Stallergenes S.A.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2010-08-16
• Last Update Posted: 27 January 2014

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: All
• Target Recruitment: 544

Inclusion Criteria

The main inclusion criteria are:
- Male or female outpatients aged 18 to 65 years (inclusive).
- Symptomatic birch pollen-related allergic rhinoconjunctivitis for at least the previous 2 pollen seasons requiring intake of symptomatic treatment.

- Sensitization to birch pollen demonstrated by:
•A positive SPT to birch pollen with wheal diameter > 3 mm.
•Birch pollen allergens specific IgE levels = 0.70 kU/L.
- RRTSS based on the previous or on the penultimate birch pollen season = 12 out of a maximum possible score of 18.
- Patients with an FEV1 = 80% of the predicted value.
- Patients who are willing to comply with the protocol.
- Patients having given a signed informed consent before completing any study related procedure.

Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 544
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Exclusion Criteria:
-Patients with symptoms of rhinitis/rhinoconjunctivitis during the birch pollen season due to any other allergens (except alder and hazel). This includes patients with symptomatic allergic rhinitis/rhinoconjunctivitis due to cat or dog allergens, and living with these animals at home or at risk of frequent contacts with these animals (family, friends etc.) during the course of the study.
-Patient who previously received desensitization treatment to birch pollen and/or another Betulaceae sp. (for example hazel or alder) within the previous 5 years.
-Patients with ongoing treatment by immunotherapy with another allergen.
-Pregnancy (positive pregnancy test), breast-feeding.
-Female patients of childbearing potential planning a pregnancy during this study or not using a medically accepted contraceptive method (hormonal birth control [orally, injectable or by implant, for at least 2 months before enrolment], intrauterine device, spermicide used with a male condom, bilateral tubal ligation, diaphragm with spermicide, female condom, monogamous relationship with a vasectomised partner).
- Patients planning to move during the study or planning to leave the area during the birch pollen season for more than 1 week (7 consecutive days).
- Patients with moderate or severe persistent asthma (GINA 3 or 4).
- Patients with seasonal mild persistent asthma (GINA 2) necessitating treatment with inhaled glucocorticosteroids at a dose level greater than 400 mcg budesonide dose-equivalents.
- Patients with any nasal or oral condition that could interfere with the efficacy or safety assessments (such as nasal polyposis or oral inflammation).
- Patients with severe immune deficiency.
- Patients with a past or current disease, which as judged by the Investigator, may affect the patient’s participation in or outcome of this study.
- Any other disease or condition which would place a patient at undue risk by being included in the study (according to the Investigator’s opinion).
- Usual contra-indications of immunotherapy such as concomitant beta-blocker therapy whatever the route and/or immunosuppressive drugs.
- Patients treated with inhaled/systemic steroids (whatever the indication) within 4 weeks prior to Visit 1 (Screening), or with long acting systemic corticosteroids 12 weeks before Visit 1 (Screening).
- Patients under continuous corticotherapy (inhaled or systemic drugs).
- Patients following a strict low sodium diet as the study treatment contains 590 mg of sodium chloride per vial in a 10 mL solution.
- Investigators, co-Investigators, as well as their children or spouses and all study collaborators.
- Patients who have participated in any clinical trial within 3 months prior to this one.

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified