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COMPLETED
NCT02298491
PHASE4

Treatment of CNS Sarcoidosis With H.P. Acthar Gel

Sponsor: University of Maryland, Baltimore

View on ClinicalTrials.gov

Summary

The purpose of this study is to see if treatment with H.P. Acthar® Gel will result in the improvement and long-term stabilization of clinical and radiographic abnormalities that occur in patients with CNS sarcoidosis. In addition, it will also look at whether treatment will be also associated with improvement in measures of quality of life. The treatment of CNS sarcoidosis involves the use of either corticosteroids such as prednisone or potent immunosuppressive agents such as methotrexate, both which can induce severe long term side effects. The adverse effects of steroids may be avoided by treatment with adrenocorticotropic hormone (ACTH), which is available for patient use as H.P. Acthar® Gel. The efficacies of H.P. Acthar® Gel in the treatment of CNS sarcoidosis and the impact on quality of life have not been previously studied. In addition, little is known regarding the expression of immune markers in CNS sarcoidosis and the association of such markers with disease activity and response to treatment.

Official title: Clinical Biomarkers of Disease Activity and Treatment Responses in Patients With CNS Sarcoidosis Treated With H.P. Acthar Gel

Key Details

Gender

All

Age Range

Any - Any

Study Type

INTERVENTIONAL

Enrollment

4

Start Date

2016-05

Completion Date

2020-11

Last Updated

2026-04-17

Healthy Volunteers

No

Conditions

Interventions

DRUG

H.P. Acthar Gel

80 IU subcutaneously daily for 10 days then followed by 80 IU subcutaneously three times per week through Month 12

Locations (1)

University of Maryland, Baltimore

Baltimore, Maryland, United States