Calcium Channel Blocker in Myotonic Dystrophy Type 1
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Amlodipine.
- Who it may be relevant to
- Registry conditions: Myotonic Dystrophy 1. Basic parameters: 18 years — 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Calcium Channel Blocker in Myotonic Dystrophy Type 1 (CAP DM1)
Overview
This is a Phase 1 clinical trial designed to evaluate the safety and tolerability of amlodipine, a calcium channel blocker, in adults with Myotonic Dystrophy Type 1 (DM1). Amlodipine is being studied to see if it can improve muscle strength, reduce stiffness (myotonia), and improve function by modifying calcium flow in muscle cells. All participants will receive amlodipine starting at 2.5 mg daily for 2 weeks, then 5 mg for 4 weeks. After that, participants will be randomly assigned to continue on 5 mg or increase to 10 mg for an additional 4 weeks. The main goals are to assess changes in blood pressure and any adverse events to determine whether the drug is safe in this population. The study will also explore how amlodipine affects muscle strength, mobility, fatigue, and daily function using clinical tests and questionnaires. Findings will inform a future phase 2 trial.
Interventions
- Drug Amlodipine
Evaluating 2 different doses of amlodipine, after an initial titration phase (2.5 mg daily), amlodipine is increased to the target doses of 5 mg and 10 mg
Primary outcome measures
- Number of Subjects Who Provided Informed Consent [Time frame: Baseline]
- Number of Completed Study Visits [Time frame: Baseline to End of Study at week 10]
- Number of Subjects Who Completed the Study Without Drug Discontinuation [Time frame: Baseline to End of Study at week 10]
- Number of Subjects Who Completed the Study [Time frame: Baseline to End of Study at week 10]
Secondary outcome measures (2)
- Mean Change in Systolic Blood Pressure [Time frame: Baseline to End of Study at week 10]
- Number of Participants With Non-Serious Adverse Events [Time frame: Baseline to End of Study at week 10]
Eligibility criteria
Inclusion criteria
- Male or Female between the ages 18 and 65, inclusive.
- A genetically confirmed diagnosis of DM1, having a repeat expansion in the DMPK gene with at least 100 CTG repeats.
- Grip strength less than 50% predicted based on age, height, and sex.
- Video hand opening time is 4 sec or greater for at least one hand.
- Ambulatory and able to walk 10 meters.
- Willingness to discontinue anti-myotonia drugs at least 2 weeks prior to screening.
- Highly effective method of contraception in women with childbearing potential.
Exclusion criteria
- Congenital DM1 as defined by symptom onset in the first 4 weeks of life.
- Abnormal liver function tests (LFTs): alanine aminotransferase (ALT), or aspartate aminotransferase (AST) >3 x upper limit of normal. Total bilirubin > 1.5 mg/dL, or INR > 1.3, or evidence of current active or chronic infection with hepatitis C, hepatitis B or other hepatobiliary conditions other than DM1 (or attributed to DM1) that cause abnormal liver laboratory parameters (e.g., hemochromatosis, Wilson's disease, autoimmune hepatitis)
- Current or recent infection requiring antibiotic treatment within 2 weeks prior to screening.
- Abnormal vital signs, including systolic blood pressure < 90 mmHg and diastolic blood pressure < 60 mmHg.
- Treatment with concomitant medications with potential interactions with amlodipine, these may include but are not limited to sildenafil, cyclosporin, atorvastatin at high dosages (80 mg daily), simvastatin (at dosages higher than 20 mg daily) or strong inhibitors of CYP3A4.
- A history of syncope.
- A history of symptomatic hypotension.
- Initiation or change in doses of concomitant medications, including herbal supplements, if in the opinion of the Investigator, may impact the results of the study.
- Women of childbearing potential must have a negative pregnancy test, cannot be planning a pregnancy, and cannot be breastfeeding at any time during the study.
- Known history of substance and/or alcohol abuse within one year prior to screening.
- The presence of comorbidities that, in the opinion of the Investigator, may influence study results, including, but not limited to, uncontrolled diabetes, generalized or mononeuropathy of the upper extremities, or cervical radiculopathy resulting in weakness and atrophy.
- Concurrent treatment with calcium channel blocker.
- Known ischemic or non-ischemic moderate or severe heart failure as defined by symptoms suggestive of heart failure or reduced left ventricular ejection fraction (LVEF) on echocardiogram < 55%.
- Moderate or severe aortic stenosis or other obstruction of the left ventricle outflow tract.
- Known sensitivity or allergy to amlodipine.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07075965 · STUDY00010646