NCT03414086

Brief Summary

Comparing the clinical effects of Acthar Gel before and after treatment and compare it to patients with inactive disease.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Nov 2017

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 6, 2017

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

January 22, 2018

Completed
7 days until next milestone

First Posted

Study publicly available on registry

January 29, 2018

Completed
4.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 30, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 30, 2022

Completed
Last Updated

August 9, 2022

Status Verified

August 1, 2022

Enrollment Period

4.7 years

First QC Date

January 22, 2018

Last Update Submit

August 6, 2022

Conditions

Keywords

PMDM

Outcome Measures

Primary Outcomes (1)

  • 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 Outcomes (1)

  • Myositis Response Criteria

    6 Months

Study Arms (2)

Myositis in Remission

Subjects who are in remission with their myositis diagnosis.

Other: Myositis in Remission

Healthy Controls

Subjects who do not have a myositis diagnosis.

Other: Healthy Control

Interventions

Ten healthy adult patients evaluating serum, PBMC's, and RNA.

Healthy Controls

Ten patients (four who have polymyositis, six dermatomyositis) from our database who are followed in the Myositis Center. We will collect serum, PBMC's, and RNA samples will be obtained at baseline and at six months. Remission is defined as a global myositis disease activity score less than or equal to 1 on the MDAAT assessments with no new immunosuppressive drug or glucocorticoid use and no increase in dose of either in the preceding year.

Myositis in Remission

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Arthritis and Autoimmunity Center

You may qualify if:

  • 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.

You may not qualify if:

  • 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:
  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Pittsburgh

Pittsburgh, Pennsylvania, 15261, United States

Location

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    BACKGROUND
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    BACKGROUND
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  • Rider LG, Werth VP, Huber AM, Alexanderson H, Rao AP, Ruperto N, Herbelin L, Barohn R, Isenberg D, Miller FW. Measures of adult and juvenile dermatomyositis, polymyositis, and inclusion body myositis: Physician and Patient/Parent Global Activity, Manual Muscle Testing (MMT), Health Assessment Questionnaire (HAQ)/Childhood Health Assessment Questionnaire (C-HAQ), Childhood Myositis Assessment Scale (CMAS), Myositis Disease Activity Assessment Tool (MDAAT), Disease Activity Score (DAS), Short Form 36 (SF-36), Child Health Questionnaire (CHQ), physician global damage, Myositis Damage Index (MDI), Quantitative Muscle Testing (QMT), Myositis Functional Index-2 (FI-2), Myositis Activities Profile (MAP), Inclusion Body Myositis Functional Rating Scale (IBMFRS), Cutaneous Dermatomyositis Disease Area and Severity Index (CDASI), Cutaneous Assessment Tool (CAT), Dermatomyositis Skin Severity Index (DSSI), Skindex, and Dermatology Life Quality Index (DLQI). Arthritis Care Res (Hoboken). 2011 Nov;63 Suppl 11(0 11):S118-57. doi: 10.1002/acr.20532. No abstract available.

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Biospecimen

Retention: SAMPLES WITHOUT DNA

We will be collecting serum, cells, and pax gene samples.

MeSH Terms

Conditions

MyositisDermatomyositisPolymyositis

Condition Hierarchy (Ancestors)

Muscular DiseasesMusculoskeletal DiseasesNeuromuscular DiseasesNervous System DiseasesConnective Tissue DiseasesSkin and Connective Tissue DiseasesSkin Diseases

Study Officials

  • Rohit Aggarwal, MD

    University of Pittsburgh

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

January 22, 2018

First Posted

January 29, 2018

Study Start

November 6, 2017

Primary Completion

July 30, 2022

Study Completion

July 30, 2022

Last Updated

August 9, 2022

Record last verified: 2022-08

Data Sharing

IPD Sharing
Will share

Outside researchers could obtain de-identified raw research data once approved from an ancillary committee.

Shared Documents
STUDY PROTOCOL
Time Frame
Data will not be made available until afte the primary manuscript is published. Data will be available indefinitely.
Access Criteria
Approval from an ancillary committee.

Locations