Tadalafil and Sildenafil for Duchenne Muscular Dystrophy
Primary Purpose
Duchenne Muscular Dystrophy
Status
Completed
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Tadalafil
Sildenafil
Sponsored by
About this trial
This is an interventional treatment trial for Duchenne Muscular Dystrophy focused on measuring Duchenne, muscular dystrophy, tadalafil, sildenafil, muscle ischemia, exercise
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of DMD confirmed by muscle biopsy or DNA analysis
- Age 7-15y
- Ambulatory
- No clinical evidence of heart failure
Exclusion Criteria:
- Hypertension, diabetes, or heart failure by standard clinical criteria
- Elevated BNP level (>100 pg/ml)
- LVEF < 50%
- Wheelchair bound
- Cardiac rhythm disorder, specifically: rhythm other than sinus, SVT, atrial fibrillation, ventricular tachycardia
- Continuous ventilatory support
- Liver disease
- Renal impairment
- Contraindications to tadalafil or sildenafil (use of nitrates, alpha-blockers, CYP3A inhibitors, amlodipine, or other PDE5A inhibitors)
Sites / Locations
- Cedars-Sinai Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Tadalafil
Sildenafil
Arm Description
Outcomes
Primary Outcome Measures
Functional muscle ischemia
Measured by the decrease in muscle tissue oxygenation (near infrared spectroscopy) and blood flow (Doppler ultrasound) evoked by reflex sympathetic activation in exercising forearm muscle.
Secondary Outcome Measures
Cardiac Function
Echocardiogram
EKG Monitoring
48 hour Holter monitoring
6 Minute Walk Test
Physical Activity
Assessed by accelerometers
Quality of Life
PedsQL inventory
Full Information
NCT ID
NCT01359670
First Posted
May 23, 2011
Last Updated
January 10, 2020
Sponsor
Cedars-Sinai Medical Center
Collaborators
Parent Project Muscular Dystrophy
1. Study Identification
Unique Protocol Identification Number
NCT01359670
Brief Title
Tadalafil and Sildenafil for Duchenne Muscular Dystrophy
Official Title
Functional Muscle Ischemia and PDE5A Inhibition in Duchenne Muscular Dystrophy
Study Type
Interventional
2. Study Status
Record Verification Date
April 2018
Overall Recruitment Status
Completed
Study Start Date
May 2011 (undefined)
Primary Completion Date
May 2013 (Actual)
Study Completion Date
May 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Cedars-Sinai Medical Center
Collaborators
Parent Project Muscular Dystrophy
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study, supported by Parent Project Muscular Dystrophy, will determine if tadalafil or sildenafil can improve muscle blood flow during exercise in boys with Duchenne muscular dystrophy.
Detailed Description
Duchenne muscular dystrophy (DMD) is a rare, progressive and fatal muscle disease affecting boys and accounts for 80% of muscular dystrophy cases. Tadalafil and sildenafil are medications approved by the FDA for the treatment of erectile dysfunction and pulmonary hypertension. This class of medication improves muscle blood flow in a mouse model of muscular dystrophy, but their benefit to boys with DMD is unknown. The purpose of this study is to 1) determine if tadalafil or sildenafil can improve muscle blood flow during exercise in boys with DMD; and 2) to inform the design of a subsequent, randomized, multi-center trial with clinical endpoints.
The investigators will enroll boys with DMD between the ages of 7 and 15 years who are ambulatory and without clinical heart failure. Participants will undergo 6 visits over the course of 5 weeks. The initial visit will include a medical history, physical exam, echocardiogram, and blood draw to determine eligibility for the study. Boys will be given a Holter monitor (a heart monitor) to wear for 48 hours to observe any irregular heartbeats or abnormalities.
Eligible boys will be randomized to one of the two study drugs: tadalafil or sildenafil. The boys will take a low dose (0.25mg/kg) of the study drug for the first 2 days and an intermediate dose (0.5mg/kg) for the subsequent 5 days. Then, boys will take a higher dose (1.0mg/kg) of the study drug for 1 week. Tadalafil will be taken once daily and sildenafil will be taken four times daily.
Study visits will occur 2 times at baseline, 2 times during the medication, and 1 time after washout of the medication. For these visits, boys will undergo an arm blood flow and hand grip exercise protocol. In this procedure, blood flow and oxygen delivery to the forearm muscles will be measured (noninvasively) before and during application of lower body negative pressure at rest and during handgrip exercise. Lower body negative pressure stimulates the blood flow changes that normally occur when a person sits up after lying down. During these visits, boys will complete a quality of life questionnaire, echocardiogram, and 6-minute walk tests. At home, boys will wear an accelerometer to measure physical activity and a Holter monitor to check for irregular heartbeats.
For boys who wish to continue with the study, there will be an option to cross-over and complete study visits with the drug they did not originally receive.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Duchenne Muscular Dystrophy
Keywords
Duchenne, muscular dystrophy, tadalafil, sildenafil, muscle ischemia, exercise
7. Study Design
Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Tadalafil
Arm Type
Experimental
Arm Title
Sildenafil
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Tadalafil
Other Intervention Name(s)
Cialis, Adcirca
Intervention Description
Escalating dose (0.25 mg/kg, 0.5 mg/kg, 1.0 mg/kg; once daily) over 2 weeks
Intervention Type
Drug
Intervention Name(s)
Sildenafil
Other Intervention Name(s)
Viagra, Revatio
Intervention Description
Escalating dose (0.25 mg/kg, 0.5 mg/kg, 1.0 mg/kg; four times daily) over 2 weeks
Primary Outcome Measure Information:
Title
Functional muscle ischemia
Description
Measured by the decrease in muscle tissue oxygenation (near infrared spectroscopy) and blood flow (Doppler ultrasound) evoked by reflex sympathetic activation in exercising forearm muscle.
Time Frame
For 5 study visits
Secondary Outcome Measure Information:
Title
Cardiac Function
Description
Echocardiogram
Time Frame
For 5 study visits
Title
EKG Monitoring
Description
48 hour Holter monitoring
Time Frame
5 times over about 6 weeks
Title
6 Minute Walk Test
Time Frame
For 5 study visits
Title
Physical Activity
Description
Assessed by accelerometers
Time Frame
5 times over about 6-weeks
Title
Quality of Life
Description
PedsQL inventory
Time Frame
For 5 study visits
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of DMD confirmed by muscle biopsy or DNA analysis
Age 7-15y
Ambulatory
No clinical evidence of heart failure
Exclusion Criteria:
Hypertension, diabetes, or heart failure by standard clinical criteria
Elevated BNP level (>100 pg/ml)
LVEF < 50%
Wheelchair bound
Cardiac rhythm disorder, specifically: rhythm other than sinus, SVT, atrial fibrillation, ventricular tachycardia
Continuous ventilatory support
Liver disease
Renal impairment
Contraindications to tadalafil or sildenafil (use of nitrates, alpha-blockers, CYP3A inhibitors, amlodipine, or other PDE5A inhibitors)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ronald Victor, MD
Organizational Affiliation
Cedars-Sinai Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cedars-Sinai Medical Center
City
Los Angeles
State/Province
California
ZIP/Postal Code
90048
Country
United States
12. IPD Sharing Statement
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Tadalafil and Sildenafil for Duchenne Muscular Dystrophy
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