Pulse ACTH vs. MP for MS

Completed · Phase 1

Conditions studied: Multiple Sclerosis

In brief

We hypothesize that corticotropin or adrenocorticotrophic hormone (ACTH), administered as Acthar Gel® (MANUFACTURER NAME) is effective in the control of clinical disease activity as a pulse therapy for relapsing-remitting MS when added to standard treatment with beta-interferon. We wish to determine whether ACTH, when administered as clustered monthly intramuscular injections (monthly pulse therapy) as add-on to beta-interferons, may be a safe and effective alternative to monthly pulse therapy with MP. In addition, we hypothesize that pulse therapy with ACTH alters immune function to favor a regulatory, rather than a pro-inflammatory T cell environment.

Key facts

Study ID

NCT01049451

Run by

University of Southern California

People needed

23

Starts

2009-11-01

Expected to finish

2013-07-01

Last updated by the study team

2017-04-19

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Clinically definite multiple sclerosis defined by McDonald Criteria.
• Between 18-65 years of age.
• Subject must able to understand and sign the IRB- approved informed consent form prior to the performance of any study-specific procedures and is willing to comply with the required scheduling and assessments of the protocol, including self-administration of study drug (if assigned to the ACTH arm).
• Subjects who are women of childbearing potential, must have a negative serum pregnancy test at the screening visit, and must be willing to practice a reliable birth-control method.
• Subjects must have at least one MS relapse within last year and/or at least one new T2 or Gadolinium-enhanced lesion on MRI while on stable interferon therapy.
• EDSS (Expanded Disability Status Scale) score of 3.0 - 6.5
• Currently on one of the approved beta-interferon drugs (Avonex, Betaseron, or Rebif) for a minimum of 6 months.

You may not qualify if…

• Women who are either pregnant or breastfeeding, and women of child-bearing potential (defined as not surgically sterile or at least two years post menopausal) who are not using one of the following birth control methods: tubal ligation, implantable contraception device, oral, patch, injectable or transdermal contraceptive, barrier method or sexual activity restricted to vasectomized partner.
• Uncontrolled hypertension, clinically significant cardiac arrhythmias, gastrointestinal ulcer, uncontrolled diabetes mellitus, osteoporosis, any stage of renal failure, psychiatric disorders or any other clinically significant general health conditions that may interfere with the trial participation.
• Subject has a history of drug or alcohol abuse within the past year.
• Subject had corticosteroid treatment within last 90 days.
• Subject started new medication within last 30 days.
• Subject is on Tysabri treatment presently or within 6 months of screening.
• Subject is on Novantrone, Cellcept, Rituxan or other chemotherapeutic treatment presently or within 6 months of screening.
• Subject is a participant in another research project.
• Subject has contraindications for either ACTH or MP administration.

Where it is running

• USC MS Center — Los Angeles, California, United States

Full record on ClinicalTrials.gov

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