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SarcoidosisPhase 2/3NCT02155803

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

A Phase 2/3 study testing ACTHAR Gel (adrenocorticotropic hormone) in people with Sarcoidosis and Hypercalcemia Due to Sarcoidosis, run by Albany Medical College at 1 site in United States.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

ACTHAR Gel has activity in sarcoidosis associated hypercalciuria and calcium dysregulation. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Sarcoidosis, Hypercalcemia Due to Sarcoidosis
What is being tested?
ACTHAR Gel (adrenocorticotropic hormone)
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
10 participants
Where
1 siteUnited States
Study dates
Feb 2015to Nov 2015
Phase
Phase 2/3
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age greater than 18 years old.
  • Able to understand English to the point of comprehending the informed consent form.
  • Biopsy proven sarcoidosis.
  • Documented hypercalciuria (urinary excretion of > 4mg/kg of calcium/day) or hypercalcemia within 4 weeks of study entry.
  • 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.

Who cannot join

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

Trial locations and contacts

1 site in 1 country.

Haroon Chaudhry, MBBS contact

518-262-1542

chaudhh@mail.amc.edu

Marc A. Judson, MD contact

518-262-5196

judsonm@mail.amc.edu

United States1 site
  • Albany Medical College

    Albany, New York, 12208

    Haroon Chaudhry, MBBS, 518-262-1542, chaudhh@mail.amc.edu

    Marc A. Judson, MD

Other trials in United States

About this study

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

Read the 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.
Being tested
ACTHAR Gel (adrenocorticotropic hormone)
Keywords
Sarcoidosis-Associated Calcium Dysregulation, Sarcoidosis-Associated hypercalciuria, hypercalcemia, hypercalciuria, nephrocalcinosis, nephrolithiasis, interstitial nephritis, glomerulonephritis, acute kidney disease, chronic kidney disease
Medical subject headings
Sarcoidosis, Hypercalcemia, Hypercalciuria, Nephrocalcinosis, Nephrolithiasis, Nephritis, Interstitial, Glomerulonephritis, Renal Insufficiency, Chronic

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ACTHAR Gel (adrenocorticotropic hormone)Drug

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

Study groups in NCT02155803
Study groupRoleWhat they receive
Sarcoidosis related Calcium DysregulationExperimentalSubjects with Sarcoidosis associated calcium dysregulation will be administered 80 units of Acthar Gel (adrenocorticotropic hormone) twice a week for 12 weeks. Clinical visits will be scheduled for -30 days, day of 1st dose and 4,8,12 and 16 week after 1st dose to monitor the health of subjects.
Receives: Drug: ACTHAR Gel (adrenocorticotropic hormone)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Reduction of 24 hour urine calcium

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

    Measured: Between week 0 and week 12.

Secondary outcomes (9)
  1. Change in serum calcium during 12 week ACTHAR GEL treatment

    Measured: Baseline compared to 12 weeks.

  2. Change in 1,25 di-hydroxy Vitamin D during 12 week ACTHAR GEL treatment

    Measured: Baseline compared to 12 weeks.

  3. Change in patient global VAS during 12 week ACTHAR GEL treatment

    Measured: Baseline to 12 weeks

  4. Change in physician global VAS during 12 week ACTHAR GEL treatment

    Measured: Baseline to 12 Weeks

  5. Change in urinary symptoms during 12 week ACTHAR GEL treatment

    Measured: Baseline to 12 Weeks

  6. Change in Short Form-36 during 12 week ACTHAR GEL treatment

    Measured: Baseline to 12 Weeks

  7. Change in Sarcoidosis Health Questionnaire during 12 week ACTHAR GEL treatment

    Measured: Baseline to 12 Weeks

  8. Change in eCOST during 12 week ACTHAR gel treatment

    Measured: Baseline to 12 Weeks

  9. Change in adjusted eCOST (eCOSTadj) calculated as the eCOST/# organs with an eCOST score > 022 during 12 week ACTHAR gel treatment

    Measured: Baseline to 12 Weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Jun 2014 (estimated)
  2. Study startFeb 2015
  3. Primary completionJun 2015 (estimated)
  4. Study completionNov 2015 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2/3
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
10 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02155803
Sponsor's protocol ID
AMCMAJCA2014
Status last verified
Jan 2015
First submitted
30 May 2014
Last updated
26 Jan 2015
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A Phase 2/3 study testing ACTHAR Gel (adrenocorticotropic hormone) in people with Sarcoidosis and Hypercalcemia Due to Sarcoidosis, run by Albany Medical College at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 26 Jan 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this combined phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Haroon Chaudhry, MBBS (518-262-1542, chaudhh@mail.amc.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Reduction of 24 hour urine calcium (time frame: Between week 0 and week 12.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Jan 2015.

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