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GSK-203162




An escalating dose, randomized, placebo-controlled, incomplete-block, 2-period cross-over study to assess the dose response for topical efficacy via airway responsiveness to adenosine-5'-monophosphate (AMP) challenge and the dose response for systemic activity via 24h plasma cortisol suppression and thereby the relative therapeutic index for fluticasone furoate (FF), fluticasone propionate (FP) and budesonide (BUD) in asthmatic subjects
fluticasone furoate; fluticasone propionate
203162
NCT02991859 2016-003002-14
Asthma
Phase 2
The data for this study is available in CDISC format.
June 2020