- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT00720382
A Study to Evaluate the Safety and Tolerability of a Nasal Spray to Treat Perennial Allergic Rhinitis
Active Controlled Trial of the Safety and Tolerability of MP 03-036 (Astepro 0.15%) in Patients With Perennial Allergic Rhinitis
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Réel)
Phase
- Phase 3
Contacts et emplacements
Lieux d'étude
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Alabama
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Oxford, Alabama, États-Unis, 36203
- Center of Research Excellence, LLC
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California
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Fountain Valley, California, États-Unis, 92708
- AABI Associates Medical Group
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Huntington Beach, California, États-Unis, 92647
- Allergy and Asthma Specialist Medical Group
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Long Beach, California, États-Unis, 90806
- West Coast Clinical Trials
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Los Angeles, California, États-Unis, 90025
- Allergy Research Foundation
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Mission Viejo, California, États-Unis, 92691
- Southern California Research
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San Diego, California, États-Unis, 92120
- Allergy Associates Medical Group Inc
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San Diego, California, États-Unis, 92123
- Allergy and Asthma Medical Group and Research Center
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San Jose, California, États-Unis, 95117
- Allergy & Asthma Associates of Santa Clara Valley Research Cntr
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Stockton, California, États-Unis, 95207
- Bensch Research Associates
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Walnut Creek, California, États-Unis, 94598
- Allergy and Asthma Clinical Research, Inc.
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Colorado
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Colorado Springs, Colorado, États-Unis, 80907
- Asthma and Allergy Associates
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Florida
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Ocala, Florida, États-Unis, 34471
- Allergy and Asthma Care of Florida
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Tallahassee, Florida, États-Unis, 32308
- Allergy and Asthma DTC
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Georgia
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Albany, Georgia, États-Unis, 31707
- Georgia Pollens Clinical Research Centers Inc
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Savannah, Georgia, États-Unis, 31406
- Aeroallergy Research Laboratories of Savannah
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Stockbridge, Georgia, États-Unis, 30281
- Clinical Research Atlanta
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Illinois
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Normal, Illinois, États-Unis, 61761
- Sneeze, Wheeze and Itch Associates
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Kansas
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Overland Park, Kansas, États-Unis, 66210
- Kansas City Allergy and Asthma
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Louisiana
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Metairie, Louisiana, États-Unis, 70001
- RX R+D
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Maryland
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Wheaton, Maryland, États-Unis, 20902
- Institute for Asthma and Allergy PC
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Massachusetts
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North Dartmouth, Massachusetts, États-Unis, 02747
- Northeast Medical Research Associates
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Minnesota
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Minneapolis, Minnesota, États-Unis, 55402
- Clinical Research Institute
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Plymouth, Minnesota, États-Unis, 55441
- Clinical Research Institute
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Missouri
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St. Louis, Missouri, États-Unis, 63141
- The Clinical Research Center
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Nebraska
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Papillion, Nebraska, États-Unis, 68046
- The Asthma and Allergy Center
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Nevada
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Henderson, Nevada, États-Unis, 89052
- Las Vegas Physicians Research Group
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New Jersey
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Mount Laurel, New Jersey, États-Unis, 08054
- Allergy and Asthma Research NJ inc
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Ocean, New Jersey, États-Unis, 07712
- Atlantic Research Center
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Teaneck, New Jersey, États-Unis, 07666
- Dr. Perin
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New York
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North Syracuse, New York, États-Unis, 13212
- Medical Research Associates of CNY, PLLC
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Rochester, New York, États-Unis, 14618
- AAIR Research Center
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North Carolina
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Raleigh, North Carolina, États-Unis, 27612
- Wake Research Associates, LLC
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Raleigh, North Carolina, États-Unis, 27607
- North Carolina Clinical Research
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Ohio
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Cincinnati, Ohio, États-Unis, 45231
- Bernstein Clinical Research Center
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Cincinnati, Ohio, États-Unis, 45252
- New Horizon's Clinical Research
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Oklahoma
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Edmond, Oklahoma, États-Unis, 73003
- Oklahoma Institute of Allergy and Asthma Clinical
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Oklahoma City, Oklahoma, États-Unis, 73120
- Allergy, Asthma and Clinical Research Center
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Oregon
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Lake Oswego, Oregon, États-Unis, 97035
- Allergy Asthma and Dermatology Research
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Medford, Oregon, États-Unis, 97504
- Clinical Research Institute of Southern Oregon, PC
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Pennsylvania
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Blue Bell, Pennsylvania, États-Unis, 19422
- Allergy and Asthma Specialist PC
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Collegeville, Pennsylvania, États-Unis, 19426
- Allergy and Consultants of NJ/PA
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Pittsburgh, Pennsylvania, États-Unis, 15241
- Allergy and Clinical Immunology Associates
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Upland, Pennsylvania, États-Unis, 19013
- Asthma and Allergy Research Associate
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Rhode Island
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Providence, Rhode Island, États-Unis, 02906
- Asthma, Nasal Disease & Allergy Research Center of New England
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South Carolina
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Charleston, South Carolina, États-Unis, 29407
- National Allergy, Asthma and Urticaria of Charleston
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Texas
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Austin, Texas, États-Unis, 78731
- Allergy and Asthma Associates
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Dallas, Texas, États-Unis, 75231
- AARA Research Center
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Dallas, Texas, États-Unis, 75231
- Pharmaceutical Research & Consulting Inc
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El Paso, Texas, États-Unis, 79902
- Western Sky Medical Research
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Houston, Texas, États-Unis, 77074
- SWAAA Research Center
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New Braunfels, Texas, États-Unis, 78130
- Central Texas Health Research
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San Antonio, Texas, États-Unis, 78229
- Biogenics Research Institute
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San Antonio, Texas, États-Unis, 78229
- Sylvana Research Associates
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San Antonio, Texas, États-Unis, 78233
- Live Oak Allergy and Asthma Clinic
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Waco, Texas, États-Unis, 76712
- Allergy Asthma Research Institute
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Virginia
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Richmond, Virginia, États-Unis, 23229
- VA Adult and Pediatric Allergy and Asthma
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Washington
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Seattle, Washington, États-Unis, 98105
- ASTHMA, Inc.
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Wisconsin
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Milwaukee, Wisconsin, États-Unis, 53209
- Advanced Healthcare
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- Male and female patients 12 years and older with a compatible history greater than or equal to 1 year of rhinitis due to perennial allergies.
- Must be willing and able to provide informed consent and to participate in all study procedures
- Must be in generally good health
- Positive skin test to a prevalent perennial allergen
Exclusion Criteria:
- On nasal examination, the presence of nasal mucosal erosion, nasal ulceration or nasal septal perforation
- Use of any investigational drug within 30 days of the first visit
- Any nasal surgery or sinus surgery within the previous year
- Presence of any hypersensitivity to drugs similar to azelastine or mometasone furoate and to either sorbital or sucralose
- Women who are pregnant or nursing
- Women who are not using an acceptable method of birth control
- Nasal Diseases likely to affect deposition of intranasal medication, such as sinusitis, rhinitis medicamentosa or clinically significant nasal polyposis or nasal structural abnormalities.
- Asthma or other lung diseases such as COPD. Mild asthma symptoms may be considered after consultation with investigator.
- Patients with Arrythmia
- Patients with know history of alcohol and drug abuse
- Existence of any surgical or medical condition, which in the opinion of the investigator or sponsor, might significantly alter the evaluation of the study.
- Use of medications that could affect the study results
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: 1
0.15% azelastine hydrochloride 1644 mcg
|
1644 mcg (205.5 mcg/spray) 2 sprays per nostril twice a day/AM and PM
|
|
Expérimental: 2
Mometasone furoate 200 mcg
|
200 mcg (50 mcg/spray) 2 sprays per nostril Once a day (AM)
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Change From Baseline on Direct Visual Nasal Exams to 12 Months
Délai: Change from baseline to 12 months
|
Examination of head and neck (scale: None, Mild, Moderate, Severe) for Epistaxis, Mucosal Edema, Nasal Discharge, Mucosal erythema, Mucosal Bleeding, and Crusting of mucosa.
Nasal irritation was rated: 0 = None, Grade 1A = focal irritation, Grade 1B = superficial mucosal erosion, Grade 2 = moderate mucosal erosion, Grade 3 = ulceration, Grade 4 = septal perforation
|
Change from baseline to 12 months
|
Autres mesures de résultats
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Change From Baseline to 12 Months in the Rhinoconjunctivitis Quality of Life Questionnaire (RQLQ) Compared to Placebo in Subjects 18 Years of Age and Older
Délai: change from baseline to 12 months
|
A 28-item RQLQ was completed on Day 1, Month 1, Month 3, Month 6, month 9 and month 12 or Early termination. The RQLQ consists of 7 domains rated on a 7 point scale with 0 being not troubled by the allergy symptoms, and 6 being extremely troubled/all of the time. Domain score will be calculated from the mean score of all items in the domain. Overall score will be calculated from the mean score of all items. |
change from baseline to 12 months
|
Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Directeur d'études: Lewis M. Fredane, MD, Meda Pharmaceuticals
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Infections
- Infections des voies respiratoires
- Maladies des voies respiratoires
- Maladies du système immunitaire
- Hypersensibilité immédiate
- Maladies oto-rhino-laryngologiques
- Hypersensibilité respiratoire
- Hypersensibilité
- Maladies du nez
- Rhinite
- Rhinite allergique
- Rhinite, allergique, pérenne
- Effets physiologiques des médicaments
- Agents neurotransmetteurs
- Mécanismes moléculaires de l'action pharmacologique
- Agents autonomes
- Agents du système nerveux périphérique
- Inhibiteurs d'enzymes
- Agents anti-inflammatoires
- Agents dermatologiques
- Agents bronchodilatateurs
- Agents anti-asthmatiques
- Agents du système respiratoire
- Agents anti-allergiques
- Antagonistes de l'histamine H1
- Antagonistes de l'histamine
- Agents d'histamine
- Antagonistes de l'histamine H1, non sédatifs
- Inhibiteurs de la lipoxygénase
- Furoate de mométasone
- Azélastine
Autres numéros d'identification d'étude
- MP436
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