Aerosol Cyclosporine in Chronic Obstructive Pulmonary Disease (COPD)

University of Pittsburgh

Status and phase

Completed

Phase 1

Conditions

Chronic Obstructive Pulmonary Disease

Treatments

Drug: Cyclosporine

Drug: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT00783107

0611109

Details and patient eligibility

About

This is a randomized, double-blinded, Phase I dose escalation-deescalation protocol (DEP) of cyclosporine inhalation solution in patients with Gold Stage III chronic obstructive pulmonary disease.

The purpose of the study is to evaluate the safety and effectiveness of aerosolized Cyclosporine in treating COPD.

The specific aims of the study are:

To identify the short term (28 day) safety profile of CyIS immunotherapy in severe COPD (GOLD III) patients with particular attention to airway reactivity and infection risk.
To identify the pharmacokinetic-pharmacodynamic relationship of CyIS using peripheral blood markers of an adaptive immune response as endpoints in subjects with severe COPD (GOLD III) treated short-term.

Subjects between 45 and 70 years of age with a confirmed diagnosis of COPD, Gold Stage III, and meet all the study requirements, will be enrolled in this study. A total of 24 subjects of either sex will be enrolled in this study. A total of 4 subject cohorts (n=6) will participate in the protocol.

Enrollment

8 patients

Sex

All

Ages

45 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age between 45 and 70 years.
A confirmed diagnosis of COPD, Gold Stage III, using current accepted diagnostic criteria, including clinical/laboratory findings, pulmonary function tests, and appropriate history to exclude other disorders that could explain their lung disease.
Subjects agree to maintain a stable medication regimen in the absence of a disease flare
ECOG performance status of 0, 1, or 2.
pCO2 < 45 mm Hg, room air oxyhemoglobin saturation > 85%
A willingness to participate in all portions of the protocol, including serial bronchoscopy, requisite surveillances, and ancillary immunologic studies in follow-up visits at this institution.
For woman of childbearing age, a negative pregnancy test, and a willingness to use two methods of contraception, or abstinence, and undergo monthly pregnancy testing.
Elevated T-cell cytokine gene expression, defined as baseline values > the mean of the pilot Gold 0-1 study population for one variable (CD4+IL-2 >23%, CD8+IFN-g >17%, CD8+MHC > 6%, or CD8 TGF-b).
An ability and willingness to provide written informed consent.

Exclusion criteria

Three, or more exacerbations of lower respiratory disease in the past year requiring systemic corticosteroids, or one exacerbation requiring hospitalization in the past 6 months
Intubation for COPD, or other cause of respiratory failure in the past year
Use of immunosuppressive therapy (including oral prednisone), other than aerosolized corticosteroids, anytime within three months prior to participation
Evidence for an opportunistic infection/colonization of the airways, i.e., non-bacterial
Use of aerosolized corticosteroids with an inability to maintain inhaled corticosteroid therapy dosing without change during the study interval
Evidence for systemic illness including hematologic disorders (defined by an absolute neutrophil count (ANC) < 4000 /mL and platelets < 120,000/mL), renal insufficiency (serum creatinine > 2.0 mg/dL), cirrhosis, or hepatic insufficiency (total bilirubin, or alkaline phosphatase > 1.5 x normal, SGOT, or SGPT > 1.2 x normal values), or a coagulopathy (INR > 1.4), seizure disorder.
Evidence for systemic abnormal renal function manifested by uncontrolled hypertension (systolic blood pressure > 160mmHg or diastolic blood pressure >90mmHg), hyperkalemia (serum creatinine > 5.0 meq/dl, and/or elevated serum creatinine above the normal range for the subject's age.
Evidence of coronary artery disease by history, e.g., angina or history of myocardial infarction within the past 12 months, unless corrected by CABG within < 5 years, and asymptomatic since
Pregnant or breast feeding females or women of childbearing potential not practicing birth control during and for 6 months following treatment, or fertile and sexually active males unwilling to use contraceptive techniques during and for 6 months following treatment
Positive HIV, or hepatitis B or C serology, or another active infection
Current or past history of cancer excluding basal or squamous cell skin cancer
Undiagnosed pulmonary nodule requiring diagnostic evaluation
Weight loss > 10% usual body weight over the past 6 months or a BMI < 18
Known hypersensitivity or allergy to propylene glycol, CsA, or lidocaine
Concurrent enrollment or participation within the prior month in other clinical trials
Greater than 15% or 200 ml reduction in FEV1 post test dose propylene glycol administration
Known medical or psychological condition (severe personality disorder or mental illness) that would not permit the subject to complete the trial or sign informed consent
Autoimmune disorders or other disorders with suspected systemic immune involvement
Active smoking history or urinary cotinine > 2.
Hypersensitivity to midazolam or narcotics which would not allow bronchoscopy sedation