ACTH Gel Therapy in Rheumatoid Arthritis

N/ACompletedNCT02030028

Dana Ascherman18 enrolled

Overview

The purpose of this research study is to evaluate if the study drug, ACTH Gel helps decrease the disease symptoms in people with Rheumatoid Arthritis (RA) who are already taking medications prescribed by their physician and are still experiencing disease symptoms. ACTH gel has been a Food and Drug Administration-approved treatment for Rheumatoid Arthritis since 1952, and in 2010 the FDA retained RA as a disease approved for ACTH gel use. Despite its FDA approval there is very limited data on its how well ACTH gel works in improving the symptoms of people with RA.

This study is for people who are currently taking a biologic therapy for Rheumatoid Arthritis and who are still experiencing symptoms. Subjects are given the ACTH gel to take twice each week for 12 weeks as a supplement to current therapies. Subjects are required to visit the clinic for a baseline visit, at 2 weeks, 4 weeks, 8 weeks and 12 weeks. We will obtain a blood sample for research purposes.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Rheumatoid Arthritis

Interventions

ACTHAR gelDRUG

Subjects are given the ACTHAR gel subcutaneously twice per week for 12 weeks.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 100 Years

Medical Language ↔ Plain English

Inclusion Criteria: * 18 year of age and older * RA diagnosis by American College of Rheumatology criteria * Active disease (CDAI \> 10) * Have received at least are biologic agent for at least 6 months * May or may not be receiving oral daily steroids (less than or equal to 20 mg/day) of prednisone equivalent * No current active infections requiring antibiotics * Patients must be on stable doses of RA therapies (e.g., methotrexate or other RA therapies for at least 4 weeks prior to baseline visit) Exclusion Criteria: * Less than 18 years of age * Unable or unwilling to give Informed Consent * Have an active infection requiring the use of antibiotics * Women who are pregnant * Uncontrolled hypertension * Abnormal renal function * Abnormal liver function as defined by and increased Alanine transaminase (ALT,) and aspartate aminotransferase (AST) that is greater than 5 times normal.

Locations (1)

University of Pittsburgh

Pittsburgh, Pennsylvania, United States

Outcomes

Primary Outcomes

Changes in Clinical Disease Activity Index (CDAI) Between Week 0 and Week 12

percentage of participants achieving \>20% improvement in CDAI after 12 weeks of therapy (\>20% reduction in CDAI relative to baseline based on ratio of CDAI at week 12 to CDAI at week 0: CDAI Week 12/CDAI Week 0 \< 0.8 meets criteria for improvement, as lower CDAI scores represent lower disease activity)

Time frame: 12 weeks

Secondary Outcomes

Change in the Disease Activity Score (DAS28-CRP) Between Week 0 and Week 12

Change in the Disease Activity Score 28-CRP (DAS28-CRP) at week 12 relative to baseline (week 0), where lower DAS28-CRP scores at week 12 represent improvement. Scale: 0-8.61 (lower scores indicate reduced disease activity)

Time frame: 12 weeks

Changes in Acute Phase Reactants (CRP) Between Week 0 and Week 12

Changes in C-reactive protein value (mg/dl): reduction in CRP values at week 12 relative to week 0 represents improvement (week 12 CRP-baseline CRP \< 0))

Time frame: 12 weeks

Change in Acute Phase Reactants (ESR) Between Week 0 and Week 12

Change in ESR--reduction in ESR at week 12 relative to baseline (week 0) represents improvement (week 12 ESR - baseline ERS \< 0)

Time frame: 12 weeks

Patient Reported Changes in Fatigue Between Week 0 and Week 12

The FACIT-F (Functional Assessment of Chronic Illness Therapy-Fatigue) scoring metric assesses fatigue using 13 questions rated on a Likert scale of 0 (no fatigue)-4 (severe fatigue); total scores range from 0-52, with higher total scores representing more severe fatigue. The difference in FACIT-F scores between weeks 12 and week 0 (calculated as FACIT-F score week 12 minus FACIT-F score at week 0) indicates changes in fatigue relative to baseline, where reduction of FACIT-F score at week 12 represents improvement in fatigue.

Data from ClinicalTrials.gov

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