Last reviewed · How we verify
NCT00612820
An 8 Day, Randomised, Double Blind, 3-way Crossover Trial of Repeat Doses of Intranasal GSK256066 and Fluticasone Propionate in the Vienna Challenge Chamber in Subjects With Seasonal Allergic Rhinitis (SAR)
Phase 2 trial testing GSK256066 in Rhinitis, Allergic, Seasonal in 55 participants. Completed in 1 May 2008.
1 May 2008
Quick facts
| Lead sponsor | GlaxoSmithKline |
|---|---|
| Phase | Phase 2 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | crossover |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 55 |
| Start date | 1 January 2008 |
| Primary completion | 1 May 2008 |
| Estimated completion | 1 May 2008 |
| Sites | 1 location across Austria |
Drugs / interventions tested
- GSK256066 — full drug profile →
- fluticasone propionate (FLUTICASONE PROPIONATE) — full drug profile →
Conditions studied
- Rhinitis, Allergic, Seasonal — all drugs for Rhinitis, Allergic, Seasonal →
Sponsor
GlaxoSmithKline — full company profile →
Who can join
Adults 18 to 50, any sex, with Rhinitis, Allergic, Seasonal. Healthy volunteers can join.
What's being measured
Primary outcomes are the specific endpoints the trial is designed to prove or disprove.
-
Investigate effect of repeat intranasal doses of fluticasone propionate alone vs. GSK256066 + fluticasone propionate on nasal symptoms of allergic rhinitis provoked by spending 4 hours in the Vienna Challenge Chamber after morning dosing on Day 2.
Time frame: spending 4 hours in the Vienna Challenge Chamber after morning dosing on Day 2.
Sponsor's own description
This is an 8 day, randomised, double blind, 3-way crossover trial of repeat doses of intranasal GSK256066 and fluticasone propionate in the Vienna Challenge Chamber in subjects with seasonal allergic rhinitis (SAR). Approximately 60 subjects will be selected for enrolment with the intention of acquiring at least 48 evaluable subjects. Laboratory safety assessments, 12-lead electrocardiograph (ECG), vital signs and adverse event enquiries will be made throughout the study. Nasal examination, symptom scores, nasal lavage, nasal scrape and allergen challenge assessments will also be performed at various time points throughout the study.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Recent developments of phosphodiesterase inhibitors: Clinical trials, emerging indications and novel molecules.
Bondarev AD, Attwood MM, Jonsson J, Chubarev VN, et al · · 2022 · cited 52× · PMID 36506513 · DOI 10.3389/fphar.2022.1057083
Verify or expand the search:
- PubMed search for NCT00612820
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of GSK256066
Trials testing the same drug.
- NCT00549744 — Clinical Endpoint Trial Investigating Once Daily and Bronchodilator Dosing · Phase 2 · completed
- NCT00549679 — Study To Evaluate Safety And Tolerability Of GSK256066 In Chronic Obstructive Pulmonary Disease (COPD) Patients · Phase 2 · completed
- NCT00515268 — Endotoxin Challenge Study For Healthy Men and Women · Phase 1 · completed
- NCT00464568 — A 5-way Treatment Period Trial of Single Doses of Intranasal GSK256066 in Patients With Rhinitis · Phase 2 · completed
Other recruiting trials for Rhinitis, Allergic, Seasonal
Currently open trials in the same condition.
- NCT07155499 — A Clinical Trial for Evaluation of Efficacy, Safety and Immunogenicity of GNR-127 (Recombinant ABP Antigen Protein Which · Phase 1, PHASE2 · active not recruiting
Other GlaxoSmithKline trials
Trials by the same sponsor.
- NCT07569081 — A Study Evaluating the Efficacy and Safety of Momelotinib in Participants With Vacuoles, E1-enzyme, X-linked, Autoinflam · Phase 2, PHASE3 · not yet recruiting
- NCT07406347 — A Trial to Evaluate the Safety and Reactogenicity of an Investigational Pneumococcal Vaccine in Infants Receiving 3-dose · Phase 1 · not yet recruiting
- NCT07286266 — A Study to Investigate GSK5733584 Compared With Chemotherapy in Participants With Platinum-resistant Ovarian Cancer (BEH · Phase 3 · not yet recruiting
- NCT07286331 — A Study to Investigate GSK5733584 Compared With Chemotherapy in Participants With Recurrent Endometrial Cancer (BEHOLD-E · Phase 3 · not yet recruiting
- NCT07406334 — A Trial to Evaluate the Safety and Reactogenicity of an Investigational Pneumococcal Vaccine in Toddlers 12 to 15 Months · Phase 1 · not yet recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT00612820 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by GlaxoSmithKline
- Last refreshed: 2 November 2016
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00612820.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing