Clinical trial

A Phase 2 Study to Determine the Safety and Efficacy of Inhaled Dry Powder…

NCT00455130 · Syntara, Industry · Completed

Key facts

NCT number NCT00455130
Title A Phase 2 Study to Determine the Safety and Efficacy of Inhaled Dry Powder Mannitol in Cystic Fibrosis
Lead sponsor Syntara, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Cystic Fibrosis
Intervention type Drug
Interventions Inhaled mannitol
Start date Mar 1, 2004
Completion Aug 1, 2005
First posted Apr 3, 2007
Last update posted Feb 2, 2010
Countries Australia, New Zealand

At a glance

  • 1–9 Study sites
  • No 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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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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