Last updated: 11/07/2018 16:34:13
Estimate FP systemic exposure in pediatric subjects age 4-11 years following FP HFA MDI
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: Estimate FP systemic exposure in pediatric subjects age 4-11 years following FP HFA MDI
Trial description: Estimate FP systemic exposure in pediatric subjects age 4-11 years following FP HFA MDI
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:
Abstract: Effect of propellant on fluticasone propionate exposure in pediatric asthma patients. MCHTA, Rashmi, SU, Sheng-Fang, KIM, Kenneth, MILGROM, Henry, DALEY-YATES, Peter, KATHMAN, Steven, and KUNKA, Robert 33rd Annual Meeting of the American College of Clinical Pharmacology 10/3/2004 Phoenix, AZ; USA
Abstract: Fluticasone propionate s ystemic exposure from a methered dose inhaler with and without aerochamber plus spacer in pediatric asthma patients. Mehta, Rashmi 1, Collins, David , Su, Sheng-Fang , Beerahee, Misba , Daley-Yates, Peter , and Kunka, Robert 34th Annual Meeting of the American College of Clinical Pharmacology 9/11/2005 Rockville, MD; USA
Abstract: Pharmacokinetics of fluticasone propionate following a metered dose inhaler containing a hydrofluoroalkane propellant in pediatric and adult asthma patients. Mehta, R. S. Ph. D., Su, S. Ph. D., Andrews, S. S. M. S., Daley-Yates, P. Ph. D., and Kunka, R. Ph. D. 101st International Conference of the American Thoracic Society 5/20/2005 San Diego, CA; USA
Mehta R, Su S, Kim K, Milgrom H, Daley-Yates P, Kathman S and Kunka RL. Effect of Propellant on Fluticasone Propionate Exposure in Pediatric Asthma Patients. Journal of Clinical Pharmacology, 44 (10): 1193, 2004
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
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
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
2003-18-12
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
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