Last updated: 11/07/2018 16:58:39
A randomised, double blind (with respect to placebo within a device), incomplete block design study to assess the systemic pharmacodynamics and pharmacokinetics of intranasal and intravenous fluticasone propionate administered via either: a nasal aerosol in propellant HFA134a (200µg, 2400µg), an ...
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: A randomised, double blind (with respect to placebo within a device), incomplete block design study to assess the systemic pharmacodynamics and pharmacokinetics of intranasal and intravenous fluticasone propionate administered via either: a nasal aerosol in propellant HFA134a (200µg, 2400µg), an ...
Trial description: A randomised, double blind (with respect to placebo within a device), incomplete block design study to assess the systemic pharmacodynamics and pharmacokinetics of intranasal and intravenous fluticasone propionate administered via either: a nasal aerosol in propellant HFA134a (200µg, 2400µg), an ...
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Price AC, Daley-Yates PT, Wright AM, Callejas S, Negligible absolute bioavailability and no HPA-axis effects after multiple 200µg daily doses of Fluticasone propionate (FP) administered from the aqueous nasal spray (FPANS). Eur Resp J 2000; 16(31):279s
Medical condition
Rhinitis
Product
fluticasone propionate
Collaborators
Not applicable
Study date(s)
March 1999 to July 1999
Type
Not applicable
Phase
1
Participation criteria
Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
1999-01-07
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.
Additional information about the trial
Not applicable
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