A Prospective Randomized, Double Blind, Placebo-controlled, Safety and Efficacy Study of Bosentan as add-on Therapy in Progressive Pulmonary Sarcoidosis
A Prospective Randomized, Double Blind, Placebo-controlled, Safety and Efficacy Study of Bosentan as add-on Therapy in Progressive Pulmonary Sarcoidosis
Progressive pulmonary sarcoidosis occurs in up to twenty percent of patients who require persistent treatment, but available treatment options have shown considerable long-term toxicity and uncertain or unproven efficacy. In these patients, pulmonary fibrosis and pulmonary hypertension are common complications which have major prognostic impact. Endothelin-1 (ET-1) has been demonstrated to play a key role in pulmonary fibrosis and pulmonary hypertension, and a potential role in pulmonary sarcoidosis. ET-1 is a potent vasoconstrictor and can promote fibrosis, cell proliferation, and remodeling, and is pro-inflammatory. Preliminary data have shown the therapeutic potential of the endothelin receptor antagonist (ERA) bosentan in sarcoidosis associated pulmonary hypertension.
In this light, the therapeutic potential of bosentan as an add-on treatment in progressive pulmonary sarcoidosis needs to be evaluated.
Inclusion Criteria:
Signed informed consent prior to any study-mandated procedure.
Male and female patients aged > 18 and < 70 years.
Histologically proven sarcoidosis diagnosed at least one year before screening.
Diagnosis of sarcoidosis and with evidence of pulmonary parenchymal disease on chest X-ray or CT (radiological stage II, III) with or without pulmonary hypertension. Subjects with concurrent extrapulmonary sarcoidosis are encouraged to be enrolled.
Progressive disease, defined as follows:
Deterioration in the 3-12 month period prior to screening in at least two of the following criteria:
Have been receiving pre-study treatment with prednisolone (or equivalent dose of corticosteroid) as a single agent (≥ 10 mg/day) or other immunosuppressants (methotrexate, azathioprine, cyclophosphamide, TNF inhibitors, etc.) within the 3-month period immediately prior to screening. Patients must be on a stable dose of these medications for > 4 weeks before starting the study medication.
AST and ALT values within three times upper limit of normal.
Ability to communicate well with the investigator, in the local language, and to understand and comply with the requirements of the study.
Negative pregnancy test in female patients.
Adequate contraception in female patients of childbearing age.
Exclusion Criteria:
Known hypersensitivity to any excipients of the drug formulation or to bosentan.
Treatment with another investigational drug within 3 months prior to screening.
Pulmonary sarcoidosis:
Other cause of pulmonary disease:
Anamnesis of beryllium or asbestos exposition
Previous smoking (> 10 PY), or active smoker
Previous administration of bosentan
Positive results from the hepatitis serology, except for vaccinated subjects, at screening.
Positive results from the HIV serology at screening.
Malignancy requiring chemotherapy or radiation
Uncontrolled other disease like
Concomitant treatment with cyclosporine A
Concomitant treatment with tacrolimus or sirolimus
Concomitant treatment with glibenclamide
Are pregnant, nursing, or planning pregnancy during the trial or within six month period thereafter.
Have a known substance dependency (drug or alcohol within 3 years of screening).
Presumed non-compliance.
Legal incapacity or limited legal capacity at screening.