Dermatomyositis Clinical Trial
Official title:
Predictor of Clinical Response to Acthar in Myositis: Phase II of Acthar Clinical Trial
NCT number | NCT03414086 |
Other study ID # | PRO16100125 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | November 6, 2017 |
Est. completion date | July 30, 2022 |
Verified date | August 2022 |
Source | University of Pittsburgh |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Comparing the clinical effects of Acthar Gel before and after treatment and compare it to patients with inactive disease.
Status | Completed |
Enrollment | 20 |
Est. completion date | July 30, 2022 |
Est. primary completion date | July 30, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Healthy Controls: - An individual will be eligible to be a control subject if his/her age is 18 years or greater. - Myositis Remission Control Group - Definite or probable PM or DM by Bohan and Peter criteria. - PM patients must either possess a myositis-associated autoantibody or undergo adjudication for confirmation of the PM diagnosis by consensus of two experts (Aggarwal or Oddis) to ensure non-PM patients are not enrolled. This step is necessary since there are well known mimics of PM. - Age is greater than or equal to 18 years - Remission of myositis as defined by a myositis disease global activity score <1 on the MDAAT and no new immunosuppressive or glucocorticoid therapy or dose change within one year. Exclusion Criteria: - Healthy Controls: - An existing diagnosis of a CTD - A potential immune compromised state, for example, treatment with immunosuppressant or anti-rejection medication or a diagnosis of an immune deficiency disease - Myositis Remission Control Group: - Juvenile DM or PM, myositis in overlap with another connective tissue disease, cancer associated myositis, inclusion body myositis, or any other non immune mediated myopathy. - Severe muscle damage defined as a baseline global muscle damage score on the MDI (Myositis Damage Index) of greater than or equal to five centimeters on a ten centimeter VAS. - Patients with malignancy within three years of screening (except basal cell cancer or squamous cell cancer of skin. - Uncontrolled diabetes, hepatic or renal disease. |
Country | Name | City | State |
---|---|---|---|
United States | University of Pittsburgh | Pittsburgh | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
University of Pittsburgh |
United States,
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* Note: There are 46 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | IMACS Core Set Measures Improvement | The International Myositis Assessment & Clinical Studies (IMACS) definition of improvement: Three of any of the six core set measures improved by greater than or equal to twenty percent, with no more than two core set measuring by greater than or equal to twenty five percent. | 6 Months | |
Secondary | Myositis Response Criteria | This criteria yields a continuous improvement score which can be more readily extrapolated to individual response in subjects allowing correlation with baseline and longitudinal immunologic markers in these subjects. | 6 Months |
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