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ACTHAR GEL for Sarcoidosis-Associated Calcium Dysregulation: An Open-label Pilot Study

ACTHAR GEL for Sarcoidosis-Associated Calcium Dysregulation: An Open-label Pilot Study

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02155803
Enrollment
10
Registered
2014-06-04
Start date
2015-02-28
Completion date
2015-11-30
Last updated
2015-01-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypercalcemia Due to Sarcoidosis, Sarcoidosis

Keywords

Sarcoidosis-Associated Calcium Dysregulation, Sarcoidosis-Associated hypercalciuria, hypercalcemia, hypercalciuria, nephrocalcinosis, nephrolithiasis, interstitial nephritis, glomerulonephritis, acute kidney disease, chronic kidney disease

Brief summary

ACTHAR Gel has activity in sarcoidosis associated hypercalciuria and calcium dysregulation.

Detailed description

Sarcoidosis is a multisystem granulomatous disease of unknown cause. Although sarcoidosis most commonly affects the lung, it may affect any organ. Although corticosteroids are recognized as the drug of choice for sarcoidosis. ACTH(adrenocorticotropic hormone) is the only drug that is FDA-approved for this disorder. However, there is limited data on the efficacy of ACTH for this condition. Calcium metabolism is disregulated in active sarcoidosis. The primary abnormality in calcium metabolism stems from an increased 1-α hydroxylase activity in sarcoid alveolar macrophages that converts 25-hydroxyvitamin D to 1, 25-dihydroxyvitamin D, the active form of the vitamin. This can result in hypercalcemia, hypercalciuria, nephrocalcinosis, nephrolithiasis, interstitial nephritis, glomerulonephritis, acute and chronic kidney disease. Importantly, almost of the renal manifestations stem from disordered calcium metabolism. Unlike other organ manifestations of sarcoidosis, the disorder of calcium metabolism is more common in whites compared to african americans.Compared to hypercalcemia, hypercalciuria is three times more common in sarcoidosis, nevertheless, it has largely been ignored. In general, the patient with hypercalcemia should be advised to avoid sunlight, curtail intake of major sources of dietary calcium and vitamin D, and drink ample fluids.If the patient is symptomatic, serum calcium is greater than 11 mg/dl, the serum creatinine is elevated, or the patient has nephrolithiasis, drug therapy is usually required. The drug of choice is prednisone at an initial daily dose of 20 - 40 mg/day.Unfortunately, prolonged corticosteroid therapy may result in unacceptable side effects including osteoporosis. This is particularly important as elevated calcitriol observed in patients with sarcoidosis can further jeopardize bone structure by resorption. Alternative medications that have shown benefit for sarcoidosis associated calcium dysregulation have included chloroquine,hydroxychloroquine, ketoconazole. Not only may ACTHER GEL have obvious anti-inflammatory effects by resulting in corticosteroid production, but it may also activate melanocortin receptors. The melanocortin system has powerful anti-inflammatory properties that may be beneficial in the treatment of sarcoidosis. We believe that there are several specific advantages of assessing the effectiveness of anti-sarcoidosis therapy by examining sarcoidosis-associated disorders of calcium metabolism. 1. The measures of granulomatous activity (serum calcium, urinary calcium, serum 25-hydroxyvitamin D, and serum 1, 25-dihydroxyvitamin D levels) are directly related to the granulomatous inflammation of sarcoidosis. 2. These parameters can be accurately and objectively quantified. This is an important issue in sarcoidosis as the endpoint for involvement of the lungs, skin, and eyes is problematic because it is either inexact and/or not unidimensional. 3. These constituents can be easily used to clinically monitor sarcoidosis. This is not the case for other forms of sarcoidosis including involvement of the lung and skin. * Although hypercalciuria and disordered calcium metabolism is not as common a manifestation of sarcoidosis as lung involvement, there is little evidence that the anti-granulomatous response to this disease is organ specific. In a randomized double-blind placebo control trial of infliximab for pulmonary sarcoidosis, extrapulmonary sarcoidosis also responded to this therapy.

Interventions

DRUGACTHAR Gel (adrenocorticotropic hormone)

ACTHAR GEL (adrenocorticotropic hormone) 80 units subcutaneously twice weekly for 12 weeks

Sponsors

Albany Medical College
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age greater than 18 years old. 2. Able to understand English to the point of comprehending the informed consent form. 3. Biopsy proven sarcoidosis. 4. Documented hypercalciuria (urinary excretion of \> 4mg/kg of calcium/day) or hypercalcemia within 4 weeks of study entry. 5. Historical evidence that the patient's hypercalciuria/hypercalcemia is related to sarcoidosis. This should include a serum parathyroid hormone (PTH) level which is not elevated.

Exclusion criteria

1. A change in anti-sarcoidosis medications within 3 months of study entry. 2. A history of hyperparathyroidism or another non-sarcoidosis cause of hypercalcemia/hypercalciuria 3. A history of Cushing's disease. 4. Have a diagnosis of a medical disorder other than sarcoidosis that in the opinion of the investigator would complicate the evaluation of response treatment. 5. Have used any investigational drug within 1 month prior to screening or within 5 half-lives of the investigational agent, whichever is longer. 6. Use of loop or thiazide diuretics for hypertension or other disorders. 7. Chronic use of antacids.

Design outcomes

Primary

MeasureTime frameDescription
Reduction of 24 hour urine calciumBetween week 0 and week 12.Reduction of 24 hour urine calcium in patients with sarcoidosis associated hypercalciuria (primary endpoint) between week 0 and week 12.

Secondary

MeasureTime frame
Change in 1,25 di-hydroxy Vitamin D during 12 week ACTHAR GEL treatmentBaseline compared to 12 weeks.
Change in patient global VAS during 12 week ACTHAR GEL treatmentBaseline to 12 weeks
Change in physician global VAS during 12 week ACTHAR GEL treatmentBaseline to 12 Weeks
Change in urinary symptoms during 12 week ACTHAR GEL treatmentBaseline to 12 Weeks
Change in serum calcium during 12 week ACTHAR GEL treatmentBaseline compared to 12 weeks.
Change in Sarcoidosis Health Questionnaire during 12 week ACTHAR GEL treatmentBaseline to 12 Weeks
Change in eCOST during 12 week ACTHAR gel treatmentBaseline to 12 Weeks
Change in adjusted eCOST (eCOSTadj) calculated as the eCOST/# organs with an eCOST score > 022 during 12 week ACTHAR gel treatmentBaseline to 12 Weeks
Change in Short Form-36 during 12 week ACTHAR GEL treatmentBaseline to 12 Weeks

Countries

United States

Contacts

Primary ContactHaroon Chaudhry, MBBS
chaudhh@mail.amc.edu518-262-1542
Backup ContactMarc A. Judson, MD
judsonm@mail.amc.edu518-262-5196

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026