Tobramycin Inhalation Powder (TIP) Administered Once Daily Continuously Versus TIP Administered BID in 28 Day on / 28 Day Off Cycles

Stopped early · Phase 4

Conditions studied: Cystic Fibrosis

In brief

To provide efficacy and safety data comparing two dosing schedules of Tobramycin Inhalation Powder (TIP) for the treatment of pulmonary Pseudomonas aeruginosa in patients with cystic fibrosis.

Key facts

Study ID

NCT02015663

Run by

Novartis Pharmaceuticals

People needed

32

Starts

2014-01-01

Expected to finish

2014-12-01

Last updated by the study team

2017-03-29

Who can join

Age: 6 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Provide written informed consent, HIPPA (Health Insurance Portability and Accountability Act) authorization (where applicable), and assent (as appropriate) prior to the performance of any study-related procedure.
• Confirmed diagnosis of CF
• FEV1 at screening (Visit 1) ≥25% and ≤ 80% of normal predicted values for age, sex, and height
• P. aeruginosa must be present within 6 months prior to screening and at screening
• Able to comply with all protocol requirements
• Clinically stable in the opinion of the investigator

You may not qualify if…

• History of Burkholderia cenocepacia (Bcc) complex within 2 years prior to screening and/or Bcc complex at screening
• Hemoptysis more than 60 cc at any time within 30 days prior to study drug administration
• History of hearing loss or chronic tinnitus deemed clinically significant by the investigator
• Serum creatinine 2 mg/dL or greater, BUN 40 mg/dL or greater, or an abnormal urinalysis defined as 2+ or greater proteinuria at screening
• Known local or systemic hypersensitivity to aminoglycosides or inhaled antibiotics
• Patients who are unable to discontinue previously received inhaled antibiotic regimen(s) (inhaled antibiotics are not allowed other than study drug)
• Use of inhaled aminoglycosides within 28 days prior to study drug administration (Visit 2)
• Use of systemic anti-pseudomonal antibiotics within 28 days prior to study drug administration
• Use of loop diuretics within 7 days prior to study drug administration
• Administration of any investigational drug within 30 days prior to enrollment or 5 half-lives, whichever is longer
• Signs and symptoms of acute pulmonary disease, e.g , pneumonia, pneumothorax
• Hospitalization during the baseline visit
• History of malignancy
• Patients with clinically significant laboratory abnormalities (not associated with the study indication) at screening
• Patients with other clinically significant conditions (not associated with the study indication) which might interfere with the assessment of this study
• Patients or caregivers with a history of noncompliance to medical regimens and patients or caregivers who are considered potentially unreliable
• Pregnant or nursing (lactating) women
• Women of child-bearing potential, defined as all women physiologically capable of becoming pregnant, including women whose career, lifestyle, or sexual orientation precludes intercourse with a male partner and women whose partners have been sterilized by vasectomy or other means, UNLESS they are using two birth control methods.
• Other protocol-defined inclusion/exclusion criteria may apply.

Where it is running

• Novartis Investigative Site — Mobile, Alabama, United States
• Novartis Investigative Site — Los Angeles, California, United States
• Novartis Investigative Site — Sacramento, California, United States
• Novartis Investigative Site — Ventura, California, United States
• Novartis Investigative Site — Altamonte Springs, Florida, United States
• Novartis Investigative Site — Jacksonville, Florida, United States
• Novartis Investigative Site — Miami, Florida, United States
• Novartis Investigative Site — Orlando, Florida, United States
• Novartis Investigative Site — Pensacola, Florida, United States
• Novartis Investigative Site — Glenview, Illinois, United States
• Novartis Investigative Site — Indianapolis, Indiana, United States
• Novartis Investigative Site — Iowa City, Iowa, United States
• Novartis Investigative Site — St Louis, Missouri, United States
• Novartis Investigative Site — New Hyde Park, New York, United States
• Novartis Investigative Site — New York, New York, United States
• Novartis Investigative Site — Akron, Ohio, United States
• Novartis Investigative Site — Oklahoma City, Oklahoma, United States
• Novartis Investigative Site — Portland, Oregon, United States
• Novartis Investigative Site — Hershey, Pennsylvania, United States
• Novartis Investigative Site — Austin, Texas, United States
• Novartis Investigative Site — Salt Lake City, Utah, United States

Full record on ClinicalTrials.gov

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