Taste and Local Tolerance Study of NLA Nasal Spray in Patients With Allergic Rhinitis

Last updated: February 29, 2008
Sponsor: Biolipox AB
Overall Status: Completed

Phase

2

Condition

Allergies & Asthma

Rhinitis, Allergic, Perennial

Acute Rhinitis

Treatment

N/A

Clinical Study ID

NCT00533637
NLA-C004P
  • Ages 18-50
  • All Genders

Study Summary

Evaluation of NLA Nasal Spray with regard to taste perversion and local tolerance

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • 18 to 50 years of age (inclusive)

  • Body Mass Index (BMI) between 18 and 28 kg/m2

  • History of pollen-induced seasonal allergic rhinitis for at least two years andotherwise healthy

  • Elevated specific IgE to at least one aero allergen or at least one positive skin picktest (SPT)

  • Seasonal allergic rhinitis with symptoms provoked by the allergen with a correspondingelevated specific IgE or positive SPT

  • Signed written Informed Consent

Exclusion

Exclusion Criteria:

  • Perennial allergic rhinitis except for cat and/or dog sensitivity under the conditionthat these patients are not exposed to cats and dogs

  • Soy bean allergy

  • Peanut allergy

  • Smoking during the last month before study inclusion

  • Any upper respiratory tract infection during the period of 2 weeks before the start ofthe study

  • Chronic medication

  • Any medication, including herbal medicines, during their last five half-lives (t½)

  • Nasal anatomical deviations

  • Extensive use of nasal sprays as judged by the Investigator

  • Ongoing nasal symptoms as judged by the Investigator

  • Known hypersensitivity to cetirizine

  • Pregnant or breast-feeding women

  • Fertile women not using reliable methods of contraception (i.e. IUD, barrier method,hormonal contraceptives, abstinence)

  • Participation in any other investigational study in the last three months

  • Inability to adhere to the study plan

  • Previous inclusion in this study

  • Blood donation during the last three months

Study Design

Total Participants: 28
Study Start date:
September 01, 2007
Estimated Completion Date:
December 31, 2007

Study Description

Oral or intranasal antihistamines is the first line treatment for allergic rhinitis. Cetirizine is a second-generation selective antihistamine widely used in an oral formulation for the treatment of allergic rhinitis. Local administration of cetirizine has been shown to reduce symptoms after allergen challenge, and has the potential to shorten the time to onset and decrease systemic side effects. However, local irritation and nasal burning/pain has been reported after nasal administration. For the compliance of the patients taking a nasal spray, the taste and tolerance of the product is of particular importance. NLA Nasal Spray contains cetirizine in a liposomal formulation aiming to improve the tolerability. The present study aims to compare the NLA Nasal Spray with cetirizine in an aqueous formulation and placebo with regard to taste perversion and local tolerance. This will be investigated off-season in patients with seasonal allergic rhinitis after provocation with allergen.

Connect with a study center

  • Department of Otorhinolaryngology, Lund University Hospital

    Lund, SE-221 85
    Sweden

    Site Not Available

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