Loading clinical trials...
Loading clinical trials...
A Randomized, Double-blind, Placebo-controlled, Multi-center, Phase III Study of the Efficacy and Safety of 300 IR Sublingual Immunotherapy (SLIT) Administered as Allergen-based Tablets Once Daily to Adult Patients Suffering From Grass Pollen Rhinoconjunctivitis
The purpose of the study is to assess the efficacy and safety of 300 IR sublingual tablet of grass pollen allergen extract compared to placebo in adult patient with allergic rhinoconjunctivitis.
Allergy is one of the most common chronic disease in the world currently affecting between 10% and 25% of the general population. Allergies to pollens characteristically result in seasonal rhinitis symptoms and allergic rhinoconjunctivitis is characterized by sneezing, congestion, rhinorrhea, nasal or palatal itching and itchy, watery, red and swollen eyes. Even if several drugs effectively manage allergic rhinoconjunctivitis symptoms, immunotherapy is considered more appropriate for patients in whom these symptoms are not optimally controlled with relief medications. In the study, each of the six rhinoconjunctivitis symptoms (sneezing, runny nose, itchy nose, nasal congestion, itchy eyes, watery eyes) will be evaluated daily and relief medication intake (oral antihistamines, eye drop antihistamine, nasal corticosteroid, oral corticosteroid) reported daily during the grass pollen season. Efficacy and good safety profile of 300IR SLIT tablet administered once per day for approximately six months (starting 4 months before and over the season) will be demonstrated during the grass pollen season compared to placebo.
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
No
Sneeze, wheeze, and Itch Associates, LLC
Normal, Illinois, United States
University of Kentucky Medical Center
Lexington, Kentucky, United States
Allergy & Asthma Specialists, PSC
Owensboro, Kentucky, United States
Johns Hopkins University
Baltimore, Maryland, United States
Respiratory Medical Research Institute of Michigan PLC
Ypsilanti, Michigan, United States
Clinical Research of the Ozarks, Inc.
Columbia, Missouri, United States
Midwest Clinical Research LLC
St Louis, Missouri, United States
Clinical Research of the Ozarks, Inc
Warrensburg, Missouri, United States
Montana Allergy & Asthma Specialists
Billings, Montana, United States
Montana Medical Research
Missoula, Montana, United States
Start Date
October 1, 2008
Primary Completion Date
August 1, 2009
Completion Date
August 1, 2009
Last Updated
May 19, 2016
473
ACTUAL participants
300 IR
DRUG
Placebo
DRUG
Lead Sponsor
Stallergenes Greer
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and Conditions