Verapamil as Therapy for Children and Young Adults With Dravet Syndrome
This study will assess how well the drug verapamil can improve control of seizures and dysautonomia symptoms in children and young adults diagnosed with Dravet syndrome. The safety of verapamil when given with all concomitant medications will also be assessed.
|Study Design:||Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
|Official Title:||Verapamil as Adjunctive Seizure Therapy for Children and Young Adults With Dravet Syndrome|
- Seizure Frequency [ Time Frame: Baseline, 8 weeks, 12 weeks, 16 weeks, 24 weeks, and 35 weeks ] [ Designated as safety issue: No ]The primary study endpoint is GTCS seizure frequency. A reduction in the number and severity of seizures is anticipated.
- Frequency of myoclonic/absence/atypical absence seizures [ Time Frame: Baseline, 8 weeks, 12 weeks, 16 weeks, 24 weeks, and 35 weeks ] [ Designated as safety issue: No ]We anticipate a reduction in myoclonic, absence, and atypical absence seizures as well.
|Study Start Date:||April 2012|
|Estimated Study Completion Date:||April 2015|
|Estimated Primary Completion Date:||April 2015 (Final data collection date for primary outcome measure)|
Verapamil will be prepared as a solution. A 50mg/ml oral suspension may be made with immediate release tablets and either a 1:1 mixture of Ora-Sweet and Ora-Plus or a 1:1 mixture of Ora-Sweet SF and Ora-Plus will be used.
Children will start on a 4 weeks titration period:
Week 1: 1mg/kg/day divided BID Week 2: 2mg/kg/day divided BID or TID Week 3: 3mg/kg/day divided BID or TID Week 4: 4mg/kg/day divided TID
In event of adverse events, and in consultation with the family and treating physician, the dosage may be decreased to 2mg/kg/day and remain at that dose for the remainder of the study.
Dravet syndrome (DS) is a devastating form of pediatric seizure disorder (epilepsy), often related to abnormalities of one of the genes that controls sodium channel function in the brain (SCN1A). Most children with DS experience continued seizures even with optimal treatment of currently available anti-seizure therapies . Many of these seizures are prolonged, and can be life threatening.
This pilot study will assess the efficacy of verapamil in improving control of seizures in children and young adults DS. This will be done by adding verapamil as open label adjunctive therapy to medications already being given. Investigators will assess the effect of verapamil therapy on seizure control and on signs of autonomic dysfunction observable to the parents/guardians. Signs of autonomic function include body temperature regulation, sweating, heart rate, pupil size, and flushing of the skin. Iannetti, et al reported treating 2 children with clinical DS (one with an SCN1A mutation) with verapamil as adjunctive therapy . Both children had a positive clinical response persisting for a number of months. No adverse effects were noted. We have treated an additional 4 children with DS with verapamil. There have been no significant adverse effects; 3 of 4 have experienced improved seizure control for months also.
Verapamil has been shown to affect autonomic tone in patients with cardiac disorders (eg. high blood pressure, heart attack). It alters the balance between parts of the autonomic nervous system's function (called sympathetic and parasympathetic function) with a shift toward decreased sympathetic tone and increased parasympathetic (vagus nerve) tone [8, 9, 10]. Verapamil is used as an effective agent to treat certain types of autonomic headaches in both adults and children. In cluster headaches, autonomic symptoms (tearing, nasal congestion, facial sweating, papillary constriction) are prominent; verapamil is an accepted treatment [11, 12].
Intense emotion triggers seizures in a subset of children with DS. Modulation of autonomic function is likely an integral part of seizure threshold in those so affected. Children with DS have a higher rate of signs of abnormal autonomic function than do controls . Cardiac autonomic control is also altered in these children, with a shift in the balance between sympathetic (relatively overactive) and parasympathetic (relatively less active) tone . Similar findings have been identified in adults with intractable epilepsy and children with partial epilepsy [15, 16, 17]. Verapamil's action in stabilizing the balance of sympathetic and parasympathetic tone may play a role altering autonomic tone abnormalities in children with DS as well. This may be a part of the mechanism that leads to improved seizure control.
Verapamil has been in clinical use for ~ 25 years. The FDA has granted an Investigational New Drug approval for use of this medication in this population of children and young adults. Investigators propose to add it to the patient's existing medications, and evaluate potential improvement in seizure control. Potential side effects will be screened. Investigators will monitor liver function with blood tests as well as concentrations of anti-seizure medications. Verapamil and nor-verapamil levels will be assessed twice also. Testing of heart rhythm (EKG) will be done before the study starts and twice more during the study.
|Contact: Heather Wendorf, MPH, CCRCfirstname.lastname@example.org|
|Contact: Beverly S Wical, MD||651-325-2325||BWical@gillettechildrens.com|
|United States, Illinois|
|Children's Memorial Hospital||Not yet recruiting|
|Chicago, Illinois, United States, 60614|
|Contact: Linda Laux, MD 773-883-9159|
|Principal Investigator: Linda Laux, MD|
|United States, Minnesota|
|Mayo Clinic||Not yet recruiting|
|Rochester, Minnesota, United States, 55905|
|Contact: Elaine Wirrell, MD 507-284-2511|
|Principal Investigator: Elaine Wirrell, MD|
|Gillette Children's Specialty Healthcare||Recruiting|
|St. Paul, Minnesota, United States, 55101|
|Contact: Heather Wendorf, MPH, CCRC 651-325-2314 email@example.com|
|Contact: Beverly Wical, M.D. 651-325-2325 BWical@gillettechildrens.com|
|Principal Investigator: Beverly S Wical, M.D.|
|Sub-Investigator: Timothy Feyma, MD|
|United States, New Hampshire|
|Mary Hitchcock Memorial Hospital||Not yet recruiting|
|Lebanon, New Hampshire, United States, 03756|
|Contact: Julie A Bursey 603-653-9948 Julie.A.Bursey@hitchcock.org|
|Contact: Richard P Morse, MD Richard.P.Morse@hitchcock.org|
|Principal Investigator: Richard P Morse, MD|
|Principal Investigator:||Beverly S Wical, MD||Gillette Children's Specialty Healthcare|