Cystic Fibrosis Clinical Trial
Official title:
Indirect Comparison of Tobramycin Solution for Inhalation Versus Aztreonam Lysine for Inhalation in the Treatment of Cystic Fibrosis
| NCT number | NCT01460836 |
| Other study ID # | HEORUS0017 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | October 25, 2011 |
| Last updated | October 26, 2011 |
| Start date | April 2010 |
| Verified date | October 2011 |
| Source | Novartis |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | United States: Food and Drug Administration |
| Study type | Observational |
Matching-adjusted indirect comparison of tobramycin solution (TIS) versus aztreonam lysine (AZLI) using TIS patient level clinical trial data and AZLI aggregated clinical trial data from published literature.
| Status | Completed |
| Enrollment | 0 |
| Est. completion date | |
| Est. primary completion date | October 2010 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 6 Years and older |
| Eligibility |
Inclusion Criteria: - = 6 years of age with a documented Cystic fibrosis (CF) diagnosis, - moderate-to severe lung disease, - the ability to perform reproducible pulmonary function tests, - Pseudomonas aeruginosa (PA) airway infection. Exclusion Criteria: Other protocol-defined inclusion/exclusion criteria may apply. |
Time Perspective: Retrospective
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Novartis Pharmaceuticals |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Mean relative change in Forced Expiratory Volume in 1 second (FEV1) from baseline | Baseline, Weeks 2, 4 and 6 | No | |
| Secondary | Mean change in the density of Pseudomonas aeruginosa (PA) from baseline | Baseline, Weeks 2, 4 and 6 | No |
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