Last updated: 11/04/2018 07:03:00
Comparator Study Evaluating Patient Experience And Preference Of FFNS vs. FPNS
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Completed
Completed
Trial overview
Official title: A Randomized, Double-blind, Placebo-controlled, Active Comparator, One-Week, Cross-Over, Multicenter Study to Evaluate the Efficacy and Patient Preference of Nasal Spray Characteristics of Once-Daily, Intranasal Administration of 110mcg Fluticasone Furoate Nasal Spray and 200mcg Fluticasone Propionate Nasal Spray in Adult Subjects with Seasonal Allergic Rhinitis
Trial description: The purpose of this replicate study to FFU105924 is to provide data on subject preference of FFNS as compared with FPNS.
Primary purpose:
Treatment
Trial design:
Crossover Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Allocation:
Randomized
Primary outcomes:
Comparison of Mean change from Baseline in Daily Reflective Total Nasal Symptom Score (rTNSS) Over Each Treatment Period of Active Drug Nasal Sprays versus Placebos
Timeframe: Baseline, Treatment Period 1 (Days 1-7), Treatment Period 2 (Days 15-21)
Subject Preference of Fluticasone Furoate Nasal Spray (FFNS) versus Fluticasone Propionate Nasal Spray (FPNS) Based on Scent/Odor
Timeframe: End of Crossover Period (Day 22)
Secondary outcomes:
Comparation of Mean Change From Baseline over each Treatment Period in Daytime Reflective Total Nasal Symptom Scores (D r-TNSS) for Active Drug Nasal Sprays versus Placebos
Timeframe: Baseline, Treatment Period 1 (Days 1-7), Treatment Period 2 (Days 15-21)
Comparision of Mean Change from Baseline over each Treatment Period in Nighttime Reflective Total Nasal Symptom Scores (N-rTNSS) for Active Drug Nasal Sprays versus Placebos
Timeframe: Baseline, Treatment Period 1 (Days 1-7), Treatment Period 2 (Days 15-21)
Subject Preference of Fluticasone Furoate Nasal Spray (FFNS) versus Fluticasone Propionate Nasal Spray (FPNS) on Preference for: Leaking Out of Nose/Down Throat
Timeframe: End of Crossover Period (Day 22)
Subject Preference of Fluticasone Furoate Nasal Spray (FFNS) versus Fluticasone Propionate Nasal Spray (FPNS) on Preference for: Ease of Use
Timeframe: End of Crossover Period (Day 22)
Subject Preference of Fluticasone Furoate Nasal Spray (FFNS) versus Fluticasone Propionate Nasal Spray (FPNS) on Preference for: Gentleness of Mist
Timeframe: End of Crossover Period (Day 22)
Interventions:
Drug: FPNS
Drug: FFNS
Drug: placebo FFNS
Drug: placebo FPNS
Enrollment:
360
Observational study model:
Not applicable
Primary completion date:
2007-09-11
Time perspective:
Not applicable
Clinical publications:
EO Meltzer, C Andrews, G Journeay, J Lim, BA Prillaman, C Garris, E Philpot. Comparison of patient preference for sensory attributes of fluticasone furoate or fluticasone propionate in adults with seasonal allergic rhinitis: a randomized, placebo-controlled, double-blind study. Ann Allergy Asthma Immunol. 2010;104(4):331-338.
Medical condition
Rhinitis, Allergic, Perennial
Product
fluticasone furoate
Collaborators
Not applicable
Study date(s)
August 2007 to November 2007
Type
Interventional
Phase
4
Participation criteria
Sex
Female & Male
Age
18+ years
Accepts healthy volunteers
No
- Informed consent
- Subject has provided an appropriately signed and dated informed consent.
- Recent use (less than 1 year) of using branded (FLONASE) or generic FPNS or use of FFNS (VERAMYST).
- Significant concomitant medical conditions, defined as but not limited to:
Inclusion and exclusion criteria
Inclusion criteria:
- Informed consent
- Subject has provided an appropriately signed and dated informed consent.
- Otherwise healthy outpatient with fall allergy
- Subject is treatable on an outpatient basis.
- Age
- 18 years or age or older at time of Visit 2
- Male or eligible female
- Female subjects should not be enrolled if they plan to become pregnant during the time of study participation. A urine pregnancy test will be required of all females at all visits to determine if the subject is pregnant.
- To be eligible for entry into the study, females of childbearing potential must commit to the consistent and correct use of an acceptable method of birth control, as defined by the following:
- Abstinence
- Females of childbearing potential who are not sexually active must commit to complete abstinence from intercourse for two weeks before exposure to the study drug, throughout the clinical trial, and for a period after the trial to account for elimination of the drug (minimum of six days).
- Oral contraceptive (either combined estrogen/progestin or progestin only)
- Injectable progestogen
- Implants of levonorgestrel
- Percutaneous contraceptive patches
- Intrauterine device (IUD) or intrauterine system (IUS) with a documented failure rate of less than 1% per year,
- Male partner who is sterile (vasectomy with documentation of azoospermia) prior to the female subject's entry into the study and is the sole sexual partner for that female subject
- Double barrier method-condom or occlusive cap (diaphragm or cervical /vault caps) plus spermicide
- Estrogenic vaginal ring
- Diagnosis of SAR
- SAR is defined as follows:
- A clinical history (written or verbal) of SAR with seasonal allergy symptoms (nasal symptoms) during each of the last two fall allergy seasons, and
- A positive skin test (by prick method) to fall allergen prevalent to the geographic area during the conduct of the study, within 12 months prior to Visit 1 or at Visit 1.
- A positive skin test is defined as a wheal 3 mm larger than the diluent control for prick testing.
- In vitro tests for specific IgE (such as RAST, PRIST) will not be allowed as a diagnosis of SAR.
- Subjects who meet the above criteria and who may also have perennial allergic rhinitis or vasomotor rhinitis are eligible for randomization.
- Adequate exposure to seasonal pollen
- Subject resides within a geographical region where exposure to fall seasonal allergen is expected to be significant during the entire study period.
- Subject does not plan to travel outside this area for more than 48 hours of the study period.
- Ability to comply with study procedures
- Subject understands and is willing, able and likely to comply with study procedures and restrictions.
- Literate
- Subject must be able to read, comprehend, and record information in English.
Exclusion criteria:
- Recent use (less than 1 year) of using branded (FLONASE) or generic FPNS or use of FFNS (VERAMYST).
- Significant concomitant medical conditions, defined as but not limited to:
- A historical or current evidence of clinically significant uncontrolled disease of any body system (e.g., tuberculosis, psychological disorders, eczema). Significant is defined as any disease that, in the opinion of the investigator, would put the safety of the subject at risk through study participation or which would confound the interpretation of the study results if the disease/condition exacerbated during the study.
- A severe physical obstruction of the nose (e.g., deviated septum or nasal polyp) or nasal septal perforation that could affect the deposition of intranasal study drug
- Nasal (eg, nasal septum) injury or surgery in the last 3 months
- Asthma, with the exception of mild intermittent asthma [National Asthma Education and Prevention Program (NARPP) Guidelines, 2002].
- Rhinitis medicamentosa
- Bacterial or viral infection (e.g., common cold) of the eyes or upper respiratory tract within two weeks of Visit 1 or during the screening period
- Documented evidence of acute or significant chronic sinusitis, as determined by the individual investigator
- Current or history of glaucoma and/or cataracts or ocular herpes simplex Physical impairment that would affect subject's ability to participate safely and fully in the study
- Clinical evidence of a Candida infection of the nose
- History of psychiatric disease, intellectual deficiency, poor motivation, substance abuse (including drug and alcohol) or other conditions that will limit the validity of informed consent or that would confound the interpretation of the study results
- History of adrenal insufficiency
- History of shingles
- Chickenpox or measles: A subject is not eligible if he/she currently has chickenpox or measles, or has been exposed to chickenpox or measles during the last 3 weeks and is non-immune. If a subject develops chickenpox or measles during the study, he/she will be withdrawn from the study. If a non-immune subject is exposed to chickenpox or measles during the study, his/her continuation in the study will be at the discretion of the investigator, taking into consideration the likelihood of developing active disease.
- Use of other corticosteroids, defined as:
- Intranasal corticosteroid within four weeks prior to Visit 1.
- Inhaled, oral, intramuscular, intravenous, ocular, and/or dermatological corticosteroid (with the exception of hydrocortisone cream/ointment, 1% or less) within eight weeks prior to Visit 1.
- Use of other allergy medications within the timeframe indicated relative to Visit 1
- Intranasal cromolyn within 14 days prior to Visit 1
- Short-acting prescription and OTC antihistamines, including antihistamines contained in insomnia and 'nighttime' pain formulations taken for insomnia, within 3 days prior to Visit 1
- Long-acting antihistamines within 10 days prior to Visit 1: loratadine, desloratadine, fexofenadine, cetirizine
- Oral or intranasal decongestants within 3 days prior to Visit 1
- Intranasal, oral, or inhaled anticholinergics within 3 days prior to Visit 1
- Oral antileukotrienes within 3 days prior to Visit 1
- Subcutaneous omalizumab (Xolair) within 5 months of Visit 1
- Intranasal antihistamines (e.g. Astelin) within 2 weeks prior to Visit 1
- Use of other medications that may affect allergic rhinitis or its symptoms
- Chronic use of concomitant medications, such as tricyclic antidepressants, that would affect assessment of the effectiveness of the study drug
- Chronic use of long-acting beta-agonists (e.g., salmeterol)
- Chronic use of other intranasally administered medications (e.g., calcitonin-salmon)
- Nasal irrigation solutions
- Use of immunosuppressive medications 8 weeks prior to screening and during the study
- Use of any medications that significantly inhibit the cytochrome P450 subfamily enzyme CYP3A4, including ritonavir and ketoconazole
- Immunotherapy
- Subjects may be enrolled into the study if the immunotherapy was not initiated within 30 days of Visit 1, if the dose has remained fixed over the 30 days prior to Visit 1, and the dose will remain fixed for the duration of the study.
- Allergy/Intolerance
- Known hypersensitivity to corticosteroids or any excipients in the product
- Clinical trial/experimental medication experience
- Has recent exposure to an investigational study drug within 30 days of Visit 1
- Participation in a previous or current GSK FFNS study
- Positive or inconclusive pregnancy test or female who is breastfeeding
- Has a positive or inconclusive pregnancy test at Visit 1 or Visit 2
- Affiliation with investigational site
- Subject is a participating investigator, sub-investigator, study co-ordinator, or employee of a participating investigator, or is an immediate family member of the aforementioned.
- Current tobacco use
- Subject currently uses smoking products including cigarettes, cigars, and pipe or chewing tobacco.
Trial location(s)
Location
GSK Investigational Site
San Diego, California, United States, 92123
Status
Study Complete
Location
GSK Investigational Site
Collegeville, Pennsylvania, United States, 19426
Status
Study Complete
Location
GSK Investigational Site
Ocean, New Jersey, United States, 07712
Status
Study Complete
Location
GSK Investigational Site
Rockville Center, New York, United States, 11570
Status
Study Complete
Location
GSK Investigational Site
San Antonio, Texas, United States, 78229
Status
Study Complete
Location
GSK Investigational Site
San Francisco, California, United States, 94104
Status
Study Complete
Location
GSK Investigational Site
Bethesda, Maryland, United States, 20814
Status
Study Complete
Location
GSK Investigational Site
Ithaca, New York, United States, 14850
Status
Study Complete
Location
GSK Investigational Site
Charleston, South Carolina, United States, 29406
Status
Study Complete
Location
GSK Investigational Site
Philadelphia, Pennsylvania, United States, 19115
Status
Study Complete
Location
GSK Investigational Site
Lilburn, Georgia, United States, 30047
Status
Study Complete
Location
GSK Investigational Site
New Braunfels, Texas, United States, 78130
Status
Study Complete
Location
GSK Investigational Site
Birmingham, Alabama, United States, 35209
Status
Study Complete
Location
GSK Investigational Site
Tallahassee, Florida, United States, 32308
Status
Study Complete
Location
GSK Investigational Site
San Jose, California, United States, 95117
Status
Study Complete
Location
GSK Investigational Site
Vista, California, United States, 92083
Status
Study Complete
Location
GSK Investigational Site
Los Angeles, California, United States, 90025
Status
Study Complete
Location
GSK Investigational Site
San Diego, California, United States, 92120
Status
Study Complete
Location
GSK Investigational Site
Long Beach, California, United States, 90806
Status
Study Complete
Location
GSK Investigational Site
Philadelphia, Pennsylvania, United States, 19107
Status
Study Complete
Location
GSK Investigational Site
Phoenix, Arizona, United States, 85050
Status
Study Complete
Study documents
Clinical study report
Available language(s): English
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Results posted on ClinicalTrials.gov
Recruitment status
Completed
Actual primary completion date
2007-09-11
Actual study completion date
2007-09-11
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
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