CompletedPhase 3NCT00388505
Safety of Tobramycin Inhalation Powder (TIP) vs Tobramycin Solution for Inhalation in Patients With Cystic Fibrosis
Studying Cystic fibrosis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Novartis Pharmaceuticals
- Principal Investigator
- Michael Konstan, MDUniversity Hospitals Cleveland Medical Center
- Intervention
- Tobramycin Inhalation Powder(drug)
- Enrollment
- 517 enrolled
- Eligibility
- 6 years · All sexes
- Timeline
- 2006 – 2009
Study locations (30)
- Novartis Investigative Site, Hartford, Connecticut, United States
- Emory University CF Center, Atlanta, Georgia, United States
- Rush University Center, Chicago, Illinois, United States
- University of Louisville, Louisville, Kentucky, United States
- Novartis Investigative Site, Boston, Massachusetts, United States
- Novartis Investigative Site, Lebanon, New Hampshire, United States
- Novartis Investigative Site, Livingston, New Jersey, United States
- Novartis Investigative Site, Long Branch, New Jersey, United States
- Novartis Investigative Site, Morristown, New Jersey, United States
- Novartis Investigative Site, Somerset, New Jersey, United States
- Novartis Investigative Site, Albany, New York, United States
- Novartis Investigative Site, Buffalo, New York, United States
- Novartis Investigative Site, New Hyde Park, New York, United States
- Novartis Investigative Site, New York, New York, United States
- University of Rochester, Rochester, New York, United States
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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