Mexiletine for the Treatment of Muscle Cramps in ALS

Last updated: July 28, 2017
Sponsor: Bjorn Oskarsson, MD
Overall Status: Completed

Phase

4

Condition

Pain (Pediatric)

Myasthenia Gravis (Chronic Weakness)

Amyotrophic Lateral Sclerosis (Als)

Treatment

N/A

Clinical Study ID

NCT01811355
378164
  • Ages 21-89
  • All Genders

Study Summary

The purpose of this study is to determine if mexiletine is effective for the treatment of muscle cramps in Amyotrophic Lateral Sclerosis (ALS).

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • ALS diagnosed according to El Escorial criteria (Awaji version) as: Possible,Probable, or Definite.

  • Experiencing cramps as a moderate or severe symptom as defined by willingness to takea medication for the symptom

  • ≥2 cramps per week during run in week

  • Life expectancy > 6 months, estimated by clinician

  • Able to take drug capsule by mouth

  • No significant EKG abnormality on screening

  • aspartate aminotransferase / alanine aminotransferase <2x upper limit of normalmeasured at screening

  • Having successfully filled out the cramp diary and cramp and fasciculation scales onsix out of the last seven days of run in period

Exclusion

Exclusion Criteria:

  • Inability to communicate by telephone or email

  • Allergy/ known sensitivity to mexiletine

  • Prior use of mexiletine

  • AV block unless subject has pacemaker

  • Cardiac arrhythmia

  • Prior myocardial infarction

  • Other significant EKG abnormality

  • Liver disease

  • History of leucopenia (WBC <3,500/mm3)

  • Epilepsy

  • Other serious and unstable medical condition

  • Pregnant woman

  • Breastfeeding woman

  • Active drug or alcohol use or dependence that, in the opinion of the siteinvestigator, would interfere with adherence to study requirements

  • Use of quinidine (alone or as a component of Nuedexta®) during the study

  • Inability or unwillingness of subject to give written informed consent

  • Woman of childbearing potential, not willing to use at least two approved methods ofcontraception

  • Use of a prohibited medication during study

Study Design

Total Participants: 23
Study Start date:
May 01, 2013
Estimated Completion Date:
May 31, 2016

Study Description

Background:

Many ALS patients suffer from painful muscle cramps, but unfortunately we do not have any medication proven to help muscle cramps in ALS. Reducing the pain caused by cramps - which can be debilitating - could help people living with ALS.

Muscle cramps are sudden, painful, and involuntary contractions of a muscle. They are caused by nerve dysfunction. When we examine nerves and muscles electrically, we see cramps as bursts of high-frequency (up to150 Hz) firing of the motor nerve cells. Cramps in ALS are believed to be the result of an increase of persistent sodium currents in the sick lower motor nerve cells.

A medication called Quinine was for many years the commonly used drug for controlling cramps in ALS, but the FDA has advised against its use for cramps because of its potential risks (e.g., death). Today there is no agreement on how to treat cramps in the ALS. The American Academy of Neurology recently encouraged further studies of the treatment of muscle cramps and suggested lidocaine as one of a few drugs of special interest.

Mexiletine:

Mexiletine is a medication closely related to lidocaine that can be taken by mouth (instead of being injected). Mexiletine stops the type of sodium currents that are thought to cause muscle cramps. Mexiletine is a relatively older medication that has been extensively studied in humans. It has been shown to reduce the electrical measures of muscle cramps for other disease conditions. For example, in patients with another severe nerve disease - Machado-Joseph disease (SCA3) - mexiletine treatment led to a decrease in the average number of muscle cramps from 24 to 3 cramps per month.. The safety profile of mexiletine is good, with the most frequent side effects being nausea or other abdominal symptoms. These side effects are rare at the doses (300 mg/day) used in this study. In patients with normal heart function, mexiletine has a minimal effect on heart rhythm. In previous clinical trials, no subject developed any serious heart rate problem.

Experimental Plan:

Using multiple sites within the State of California we will quickly enroll a small number (N=30) of ALS patients with severe muscle cramps. The study is a double-blinded, placebo controlled (i.e., the investigator and the participant does not know if the pills contain mexiletine or placebo), crossover (all subjects receive two weeks of mexiletine and two weeks of placebo) study.

After a one week run in, participants will be evaluated on their ability to fill out the cramp diary. Participants who filled out their diary will be randomly assigned to either mexiletine or placebo for their first two weeks. For the first three days of each 2-week period, one 150mg capsule will be taken at bed time. For day 4 to 14 one capsule twice per day will be taken. Each treatment period will be 2 weeks with an intervening 1 week washout period - for a total study length of 6 weeks. Safety will be monitored with liver function studies and EKG's.

Connect with a study center

  • UCD Telehealth Network - Lake Almanor Clinic

    Chester, California 96020
    United States

    Site Not Available

  • UCSD Department of Neurosciences ALS Clinical Trials (ACT) Program

    La Jolla, California 92093
    United States

    Site Not Available

  • UCLA Neuromuscular Research Program

    Los Angeles, California 90095
    United States

    Site Not Available

  • UCD Telehealth Network

    Multiple Locations, California Various
    United States

    Site Not Available

  • UCD Telehealth Network

    One hundred sites, California Various
    United States

    Site Not Available

  • UC Irvine Health ALS & Neuromuscular Center

    Orange, California 92868
    United States

    Site Not Available

  • UC, Davis Medical Center ALS Clinic

    Sacramento, California 95817
    United States

    Site Not Available

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