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ClinicalTrials.gov record
Completed No phase listed Observational

Observational Study in Cystic Fibrosis Patients Using TOBI® PODHALER® or Other FDA Approved Inhaled Antipseudomonal Antibacterial Drugs

ClinicalTrials.gov ID: NCT02449031

Public ClinicalTrials.gov record NCT02449031. 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 Oct 21, 2026, 12:05 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 Prospective Observational Study in Cystic Fibrosis Patients With Chronic Respiratory Pseudomonas Aeruginosa Infection Treated With TOBI® PODHALER® (Tobramycin Inhalation Powder) or Other FDA Approved Inhaled Antipseudomonal Antibacterial Drugs

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a multicenter, prospective, two cohort, observational study over a 5-year period in Cystic Fibrosis (CF) patients with chronic Pseudomonas aeruginosa infection.The study will collect data over 1 year on respiratory function, antibacterial effectiveness, and clinical outcomes of treatment with inhaled antipseudomonal antibiotics and data over 5 years on microbiological and safety assessments.

Study identification

NCT ID
NCT02449031
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Mylan Inc.
Industry
Enrollment
409 participants

Conditions and interventions

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
May 5, 2015 (Actual)
Primary completion
Dec 31, 2021 (Actual)
Completion
Dec 31, 2021 (Actual)
Last update posted
Mar 22, 2022

2015 – 2021

United States locations

U.S. sites
47
U.S. states
32
U.S. cities
46
Facility City State ZIP Site status
Novartis Investigative Site Anchorage Alaska 99508 —
Novartis Investigative Site Little Rock Arkansas 72202 —
Novartis Investigative Site Bellflower California 90706 —
Novartis Investigative Site Fullerton California 92831 —
Novartis Investigative Site Los Angeles California 90027 —
Novartis Investigative Site Madera California 93636 —
Novartis Investigative Site Hartford Connecticut 06102 —
Novartis Investigative Site New Haven Connecticut 06519 —
Novartis Investigative Site Stamford Connecticut 06902 —
Novartis Investigative Site Gainesville Florida 32610 —
Novartis Investigative Site Miami Florida 33136 —
Novartis Investigative Site Orlando Florida 32803 —
Novartis Investigative Site Tampa Florida 33606 —
Novartis Investigative Site Atlanta Georgia 30322 —
Novartis Investigative Site Boise Idaho 83712 —
Novartis Investigative Site Chicago Illinois 60611 —
Novartis Investigative Site Indianapolis Indiana 46202-5225 —
Novartis Investigative Site Iowa City Iowa 52242 —
Novartis Investigative Site New Orleans Louisiana 70112 —
Novartis Investigative Site Boston Massachusetts 02115 —
Novartis Investigative Site Detroit Michigan 97205 —
Novartis Investigative Site Grand Rapids Michigan 49503 —
Novartis Investigative Site Ypsilanti Michigan 48197 —
Novartis Investigative Site Jackson Mississippi 39216 —
Novartis Investigative Site Kansas City Missouri 64108 —
Novartis Investigative Site Billings Montana 59101 —
Novartis Investigative Site Omaha Nebraska 68198 —
Novartis Investigative Site Lebanon New Hampshire 03756 —
Novartis Investigative Site New Brunswick New Jersey 8901 —
Novartis Investigative Site New Hyde Park New York 11040 —
Novartis Investigative Site Winston-Salem North Carolina 27157 —
Novartis Investigative Site Akron Ohio 44308-1062 —
Novartis Investigative Site Oklahoma City Oklahoma 73104 —
Novartis Investigative Site Hershey Pennsylvania 17033-085 —
Novartis Investigative Site Philadelphia Pennsylvania 19104 —
Novartis Investigative Site Philadelphia Pennsylvania 19107 —
Novartis Investigative Site Charleston South Carolina 29425 —
Novartis Investigative Site Sioux Falls South Dakota 57104 —
Novartis Investigative Site Nashville Tennessee 37232 —
Novartis Investigative Site Austin Texas 78723 —
Novartis Investigative Site Dallas Texas 75390 —
Novartis Investigative Site Tyler Texas 75708 —
Novartis Investigative Site Salt Lake City Utah 84132 —
Novartis Investigative Site Burlington Vermont 5405 —
Novartis Investigative Site Norfolk Virginia 23507 —
Novartis Investigative Site Richmond Virginia 23298 —
Novartis Investigative Site Spokane Washington 99204 —

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 NCT02449031, 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 22, 2022 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02449031 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →