Treatment of Myotonia - Lamotrigine Versus Namuscla

Non-Dystrophic Myotonia Clinical Trial

Official title:

Treatment of Myotonia - Lamotrigine Versus Namuscla

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05639257
• Other study ID #: 2021-003784-94
• Status: Recruiting
• Phase: N/A
• Start date: December 5, 2022
• Est. completion date: April 1, 2024

Study information

• Verified date: December 2022
• Source: Rigshospitalet, Denmark
• Contact: Grete Andersen
• Phone: 35453545
• Email: grete.andersen.01[@]regionh.dk
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In this clinical study, the aim is to investigate whether there is a difference in treatment of myotonia using two drugs. A difference there can justify the significantly higher cost when treated by Namuscla versus Lamotrigine.

According to the current corona pandemic, the investigators designed an app to use for data collection in the study. The app also ensures that patients who live far from the clinic more easily can participate.

Description:

On 18 May 2020, the National Board of Health in Denmark approved Namuscla for the treatment of myotonia. Myotonia is a congenital muscle disease that delays muscle relaxation after a muscle contraction. Myotonia can be disabling, but with treatment, most are able to work. Namuscla is the first registered drug to treat myotonia, however, the active part mexiletine is not new. It has been used off-label to treat myotonia for decades. The price for the new preparation is high with a daily cost (approx. 70 EU/dollar). In 2017, the investigators found evidence that treatment with lamotrigine is efficacious against myotonia. Treatment with lamotrigine can reduce the price to 150 EU/dollar per year.

Therefore, the aim of the study is to investigate whether there is a difference in the effects om myotonia and side effects of the two drugs, which can justify the significantly higher cost when treated with Namuscla in a double blinded, inferiority, cross-over study lasting 4 months.

According to the current corona pandemic, the study is designed without need of physical attendance so that inclusion and collection of experimental data can take place, by phone conversations, video-guided testing, and diary registration via a study-App. It also ensures that patients who live far away more easily can participate. Blood tests and ECGs can be performed locally.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 32
• Est. completion date: April 1, 2024
• Est. primary completion date: April 1, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Capable adult women and men (age = 18 years).

2. Diagnosed with Myotonia Congenita (Becker and Thomsen type), Paramyotonia Congenita, or Hyperkalemic periodic paralysis.

3. Myotonia under treatment or which significantly limits the daily activities (MBS> 2).

Exclusion Criteria:

1. Allergy to lamotrigine, mexiletine, or the inactive ingredients in trial medication.

2. Disease, which is affected by trial medication such as heart disease (ischemia and arrhythmia), epilepsy, and significant renal or hepatic failure.

3. Treatment that, in the opinion of the project manager, can affect the study result - medication with significant interactions with trial medication.

4. In case of smoking, start or cessation during the study.

5. Pregnant or breastfeeding during the study period. Fertile women with a positive pregnancy test at the time of entry into the trial, or who do not use safe contraception during the project period.

Related Conditions & MeSH terms

• Myotonia
• Non-Dystrophic Myotonia

Intervention

Drug:
• Lamotrigine
Lamotrigine tablets increasing dosis to maximal 300 mg daily
• Namuscla
Namuscla tablets increasing dosis to maximal 501 mg daily

Locations

Country	Name	City	State
Denmark	Copenhagen Neuromuscular Center, department of Neurology, Rigshospitalet	Copenhagen

Sponsors (6)

Lead Sponsor	Collaborator
Grete Andersen, MD	Danish Region, GCP-Copenhagen, Lupin Atlantis Holdings S.A., Region Capital Denmark, ZiteLab

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Myotonia Behavior Scale (MBS)	Each participant chose one of six statements about how myotonia affect their daily living. MBS is register once daily in a week. 1 is no symptoms of myotonia, 6 is invalidating symptoms of myotonia.; Measured without treatment and in the last week of treatment.	baseline and week 8
Secondary	Change in Eye-myotonia	Eye opening test (time in seconds): Eyes are pinched with maximum strength for 5 sec, then opened ASAP. Repeated 5 times. Longer times measured more server myotonia in eye muscles.	baseline and week 8
Secondary	Change in hand-myotonia	Hand opening test (time in seconds): Right hand is closed with maximum strength for five seconds before opened as soon as possible. Time is measured in seconds. Longer times measured more server myotonia in hand muscles. Repeated 5 times.	baseline and week 8
Secondary	Change in time-up-and-go-test (TUG)	TUG - time-up&go (time in seconds): After 10 minutes rest in a chair, participants get up, walk 3 meters, turn around, returning to the chair performed in regular pace. Longer times measured more server myotonia in legs muscles.	baseline and week 8
Secondary	Change in Individualized Neuromuscular Quality of Life Questionnaire (INQoL)	A questionnaire for patients with neuromuscular diseases measuring quality of life and the impact of the disease on everyday life. The INQoL is composed of 45 items investigating 4 dimensions, subdivided into 11 sub-dimensions. The scoring of the INQoL generates a profile (0-100). Higher score scores = higher impact of disorders. The form is translated in Danish.	baseline and week 8
Secondary	Days with Side effects (SE)	Side effects are noted daily. Participants have three opportunities they can 1) cross no SE, 2) cross a specific SE on an alphabetically list containing all known SE for both drugs, or 3) they can describe a AE under other.	through study completion, in total 123 days
Secondary	Change in Side Effect Scale (SE)	Each participant chose one of six statements about how side effects affect their daily living. SES is register once daily in a week. 1 is no side effects, 6 is invalidating side effects.	baseline and week 8