Efficacy & Tolerability of Tobramycin Podhaler in Bronchiectasis Patients With Chronic Pseudomonas Aeruginosa Infection (TOBI)
Primary Purpose
Bronchiectasis With Chronic Infection With Pseudomonas Aeruginosa
Status
Unknown status
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
Tobramycin
Sponsored by
About this trial
This is an interventional treatment trial for Bronchiectasis With Chronic Infection With Pseudomonas Aeruginosa focused on measuring Tobramycin Podhaler, bronchiectasis, chronic infection, Pseudomonas Aeruginosa
Eligibility Criteria
Inclusion Criteria:
- Patients with bronchiectasis confirmed by CT
- Chronic PA colonization with 2 documented sputum cultures positive for PA in the last 24 months.
- Age >=18
Exclusion Criteria:
- Patients diagnosed with CF
- Patients who do not tolerate Tobramycin
- Pregnant or breastfeeding
- Patients treated in the last 8 weeks with antibiotic therapy either inhaled or systemic (excluding Azenil PO x 3/week which is allowed)
Sites / Locations
- Pulmonary Institute, Rabin Medical Center, Beilinson Campus
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
TOBI / Placebo
Placebo / TOBI
Arm Description
TOBI / Placebo.
Placebo / TOBI
Outcomes
Primary Outcome Measures
Number of exacerbations as measured by number of systemic courses of antibiotics either PO or IV
Exacerbation count at 24 weeks, 48 weeks and 52 weeks
Secondary Outcome Measures
Quality of life and Symptoms Score as measured by SGRQ(Saint George's Respiratory Questionnaire) and CASA-Q-CD (Cough and Sputum Assessment Questionnaire) cough and sputum domains
Control Period Patients will visit the site 3 times every 12 weeks, TOBI Period Patients will visit the clinic at least 4 times a year during this 24 week period, when enrolled to the study during the 48 weeks period of the study
Pulmonary function tests (FEV1)
Control Period Patients will visit site 3 times every 12 weeks, TOBI Period Patients will visit the clinic at least 4 times a year during this 24 week period, when enrolled to the study during the 48 weeks period of the study
Sputum microbiology: Change in Pseudomona Aeruginosa density in sputum
Samples will be taken at every visit and changes will be analyzed at the end of the study, when enrolled to the study during the 48 weeks period of the study PENDING finding a lab that can perform this test (CFU quantitation).
Safety and Tolerability of TOBI podhaler
Adverse Events and Serious Adverse Events will be monitored continuously in the study and analyzed at the end of study, when enrolled to the study during the 48 weeks period of the study, plus 4 weeks wash-out.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02102152
Brief Title
Efficacy & Tolerability of Tobramycin Podhaler in Bronchiectasis Patients With Chronic Pseudomonas Aeruginosa Infection
Acronym
TOBI
Official Title
Efficacy & Tolerability of Tobramycin Podhaler in Bronchiectasis Patients With Chronic Pseudomonas Aeruginosa Infection
Study Type
Interventional
2. Study Status
Record Verification Date
March 2014
Overall Recruitment Status
Unknown status
Study Start Date
April 2014 (undefined)
Primary Completion Date
April 2016 (Anticipated)
Study Completion Date
May 2016 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rabin Medical Center
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The use of inhaled medications for the treatment of pulmonary diseases allows for the delivery of a high concentration of a drug at the site of disease with reduced systemic absorption and risk of systemic adverse effects. Inhaled Tobramycin has been successfully used in the maintenance treatment of CF patients with chronic colonization with PA (Pseudomonas aeruginosa). In the CF population TOBI has been proven to improve lung functions, decrease the density of the PA in the sputum, decrease hospitalizations, and reduce the risk of mortality.
Non CF Bronchiectasis share many features in common with CF, including frequent colonization with PA that leads to deterioration in lung function and increased morbidity. A recent Cochrane review concluded that there is a small benefit for the use of prolonged antibiotics in the treatment of bronchiectasis, however further randomized controlled trials with adequate power and standardized end points are required.
There have been reports in the literature describing the efficacy of inhaled tobramycin the treatment of patients with non CF bronchiectasis with eradication of PA, and significant improvement in respiratory symptoms. There were however patients who discontinued treatment due to adverse events most commonly cough wheezing and dyspnea. (Scheinberg and Shore, Chest 2005).
TOBI Podhaler is a dry powder inhaler that was recently launched, and is much easier and faster to use compared to nebulised Tobramycin. To the best of our knowledge Tobramycin dry powder formulation has not yet been trialed in patients with non CF bronchiectasis.
The purpose of this trial is to assess the efficacy and tolerability of TOBI Podhaler in patients with non CF bronchiectasis, and to gather more data on the benefit of continuous antibiotic therapy in patients with non CF bronchectais.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bronchiectasis With Chronic Infection With Pseudomonas Aeruginosa
Keywords
Tobramycin Podhaler, bronchiectasis, chronic infection, Pseudomonas Aeruginosa
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
TOBI / Placebo
Arm Type
Active Comparator
Arm Description
TOBI / Placebo.
Arm Title
Placebo / TOBI
Arm Type
Active Comparator
Arm Description
Placebo / TOBI
Intervention Type
Drug
Intervention Name(s)
Tobramycin
Primary Outcome Measure Information:
Title
Number of exacerbations as measured by number of systemic courses of antibiotics either PO or IV
Description
Exacerbation count at 24 weeks, 48 weeks and 52 weeks
Time Frame
52 weeks total
Secondary Outcome Measure Information:
Title
Quality of life and Symptoms Score as measured by SGRQ(Saint George's Respiratory Questionnaire) and CASA-Q-CD (Cough and Sputum Assessment Questionnaire) cough and sputum domains
Description
Control Period Patients will visit the site 3 times every 12 weeks, TOBI Period Patients will visit the clinic at least 4 times a year during this 24 week period, when enrolled to the study during the 48 weeks period of the study
Time Frame
52 weeks
Title
Pulmonary function tests (FEV1)
Description
Control Period Patients will visit site 3 times every 12 weeks, TOBI Period Patients will visit the clinic at least 4 times a year during this 24 week period, when enrolled to the study during the 48 weeks period of the study
Time Frame
52 weeks
Title
Sputum microbiology: Change in Pseudomona Aeruginosa density in sputum
Description
Samples will be taken at every visit and changes will be analyzed at the end of the study, when enrolled to the study during the 48 weeks period of the study PENDING finding a lab that can perform this test (CFU quantitation).
Time Frame
52 weeks
Title
Safety and Tolerability of TOBI podhaler
Description
Adverse Events and Serious Adverse Events will be monitored continuously in the study and analyzed at the end of study, when enrolled to the study during the 48 weeks period of the study, plus 4 weeks wash-out.
Time Frame
52 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with bronchiectasis confirmed by CT
Chronic PA colonization with 2 documented sputum cultures positive for PA in the last 24 months.
Age >=18
Exclusion Criteria:
Patients diagnosed with CF
Patients who do not tolerate Tobramycin
Pregnant or breastfeeding
Patients treated in the last 8 weeks with antibiotic therapy either inhaled or systemic (excluding Azenil PO x 3/week which is allowed)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mordechai Kramer, Prof
Phone
050-5710702
Email
Kremerm@clalit.org.il
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mordechai R Kramer, MD
Organizational Affiliation
Rabin Medical Center
Official's Role
Study Chair
Facility Information:
Facility Name
Pulmonary Institute, Rabin Medical Center, Beilinson Campus
City
Petach Tikva
ZIP/Postal Code
49100
Country
Israel
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mordechai Kramer, Prof
First Name & Middle Initial & Last Name & Degree
Leonardo Fuks, Dr
12. IPD Sharing Statement
Citations:
PubMed Identifier
15821224
Citation
Scheinberg P, Shore E. A pilot study of the safety and efficacy of tobramycin solution for inhalation in patients with severe bronchiectasis. Chest. 2005 Apr;127(4):1420-6. doi: 10.1378/chest.127.4.1420.
Results Reference
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PubMed Identifier
21075062
Citation
Konstan MW, Flume PA, Kappler M, Chiron R, Higgins M, Brockhaus F, Zhang J, Angyalosi G, He E, Geller DE. Safety, efficacy and convenience of tobramycin inhalation powder in cystic fibrosis patients: The EAGER trial. J Cyst Fibros. 2011 Jan;10(1):54-61. doi: 10.1016/j.jcf.2010.10.003. Epub 2010 Nov 12.
Results Reference
background
PubMed Identifier
17443506
Citation
Evans DJ, Bara AI, Greenstone M. Prolonged antibiotics for purulent bronchiectasis in children and adults. Cochrane Database Syst Rev. 2007 Apr 18;(2):CD001392. doi: 10.1002/14651858.CD001392.pub2.
Results Reference
background
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Efficacy & Tolerability of Tobramycin Podhaler in Bronchiectasis Patients With Chronic Pseudomonas Aeruginosa Infection
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