Clinical trial

Clinical Assessment Of GW815SF Salmeterol/Fluticasone Propionate(HFA MDI) In…

NCT00449046 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00449046
Title Clinical Assessment Of GW815SF Salmeterol/Fluticasone Propionate(HFA MDI) In Pediatric Patients With Bronchial Asthma -A Long Term (24-week) Study-
Official title Clinical Assessment of GW815SF Salmeterol/Fluticasone Propionate (HFA MDI) in Pediatric Patients With Bronchial Asthma -A Long Term (24-week) Study-
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Bronchial Asthma
Intervention type Drug
Interventions GW815SF Salmeterol/Fluticasone propionate(HFA MDI)
Enrollment 40
Start date Mar 1, 2007
Primary completion Nov 1, 2007
Completion Nov 1, 2007
First posted Mar 19, 2007
Last update posted May 6, 2015
Countries Japan

At a glance

  • 1–9 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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