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Terminated Phase 4 Interventional Results available

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

ClinicalTrials.gov ID: NCT02015663

Public ClinicalTrials.gov record NCT02015663. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 4:44 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A 24-week, Open-label, Parallel-group, Interventional Phase IV Study Comparing Tobramycin Inhalation Powder (TIP) Administered Once Daily Continuously Versus TIP Administered BID in 28 Day on / 28 Day Off Cycles for the Treatment of Pulmonary Pseudomonas Aeruginosa in Patients With Cystic Fibrosis

Study identification

NCT ID
NCT02015663
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
32 participants

Conditions and interventions

Interventions

  • Tobramycin Inhalation Powder Drug

Drug

Eligibility (public fields only)

Age range
6 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 31, 2013
Primary completion
Nov 30, 2014
Completion
Nov 30, 2014
Last update posted
Mar 28, 2017

2014

United States locations

U.S. sites
21
U.S. states
14
U.S. cities
21
Facility City State ZIP Site status
Novartis Investigative Site Mobile Alabama 36608-1128
Novartis Investigative Site Los Angeles California 90027
Novartis Investigative Site Sacramento California 95819
Novartis Investigative Site Ventura California 93003
Novartis Investigative Site Altamonte Springs Florida 32701
Novartis Investigative Site Jacksonville Florida 32207
Novartis Investigative Site Miami Florida 33136
Novartis Investigative Site Orlando Florida 32806
Novartis Investigative Site Pensacola Florida 32504
Novartis Investigative Site Glenview Illinois 60025
Novartis Investigative Site Indianapolis Indiana 46202
Novartis Investigative Site Iowa City Iowa 52242
Novartis Investigative Site St Louis Missouri 63104
Novartis Investigative Site New Hyde Park New York 11040
Novartis Investigative Site New York New York 10595
Novartis Investigative Site Akron Ohio 44308
Novartis Investigative Site Oklahoma City Oklahoma 73112
Novartis Investigative Site Portland Oregon 92772
Novartis Investigative Site Hershey Pennsylvania 17033-8050
Novartis Investigative Site Austin Texas 78723
Novartis Investigative Site Salt Lake City Utah 84132

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02015663, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 28, 2017 · Synced Jul 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02015663 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →