Elamipretide for Barth Syndrome
(4TAZPower Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a treatment called elamipretide for individuals with Barth Syndrome, a rare genetic condition that affects energy production in cells. Researchers aim to confirm whether this treatment can improve muscle strength, particularly in the knee. The trial includes two groups: one receiving elamipretide and the other a placebo, a harmless substance used for comparison. It suits males with a confirmed diagnosis of Barth Syndrome and stable heart health. As a Phase 4 trial, this research seeks to understand how the already FDA-approved and effective treatment benefits a broader range of patients.
Do I have to stop taking my current medications for the trial?
The trial requires that participants with a history of cardiomyopathy must be on a stable regimen of heart failure medications for at least 3 months before starting the trial. This suggests you may need to continue your current heart medications if they are stable.
What is the safety track record for elamipretide?
Studies have shown that elamipretide is generally well-tolerated by people with Barth Syndrome. Research indicates that long-term use of elamipretide leads to positive results, improving heart and muscle functions.
In a study lasting 168 weeks, patients tolerated elamipretide well and experienced improvements in physical abilities and heart health. Another review of safety data found that the main side effect was minor irritation at the injection site, with no other major safety concerns reported.
Elamipretide is also approved for treating muscle weakness, suggesting it has a known safety profile. Overall, the evidence indicates that elamipretide is a safe treatment option for those considering joining the trial.12345Why are researchers enthusiastic about this study treatment?
Elamipretide is unique because it targets the mitochondria, the energy powerhouses of cells, which is different from other treatments for Barth Syndrome that primarily focus on managing symptoms. Most existing treatments don't address the underlying energy production issues in cells, but Elamipretide aims to improve mitochondrial function directly. This novel approach has the potential to enhance energy levels and overall cell performance, offering hope for more effective management of this rare condition. Researchers are excited about Elamipretide because it could lead to significant improvements in quality of life for those affected by Barth Syndrome.
What is the effectiveness track record for elamipretide in treating Barth Syndrome?
Studies have shown that elamipretide can help treat Barth Syndrome. Earlier research demonstrated that elamipretide improved muscle strength, heart function, and exercise capacity in people with Barth Syndrome. Specifically, patients showed better physical abilities and a significant improvement in heart size and function, with over 40% improvement in heart volumes. In this trial, participants will receive either elamipretide or a placebo to further evaluate its effectiveness. Elamipretide is approved in the U.S. under the name FORZINITY™ to boost muscle strength in patients with Barth Syndrome. These improvements suggest that elamipretide can be a promising option for managing symptoms of this condition.12467
Who Is on the Research Team?
Rekha Sathyanarayana
Principal Investigator
Stealth BioTherapeutics Inc.
Are You a Good Fit for This Trial?
This trial is for males aged 5 and older with genetically confirmed Barth Syndrome, good heart function, able to follow study requirements, and not recently hospitalized for heart failure. Participants must not have severe kidney problems, active cancer, recent organ transplants (except stable heart), or allergies to the study drug.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive daily subcutaneous injections of elamipretide or placebo for 72 weeks
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Elamipretide
Trial Overview
The study tests a daily injection of elamipretide versus placebo in people with Barth Syndrome over 72 weeks. It aims to see if elamipretide improves muscle strength compared to placebo. The trial is randomized and double-blind—neither patients nor doctors know who gets which treatment.
How Is the Trial Designed?
2
Treatment groups
Active Control
Placebo Group
Elamipretide - aqueous, sterile 5.0 mL single-patient, ready to use, multi-dose glass vial containing 3.5 mL of elamipretide solution (elamipretide \[80 mg/mL\],
Matching Placebo-aqueous, sterile 5.0 mL single-patient, ready to use, multi-dose glass vial containing will be composed of 3.5mL of sodium chloride, phosphate buffer, and benzyl alcohol similar to excipients in active drug but without the active drug substance
Find a Clinic Near You
Who Is Running the Clinical Trial?
Stealth BioTherapeutics Inc.
Lead Sponsor
Citations
168-week open-label extension results of TAZPOWER
Elamipretide was associated with sustained long-term tolerability and efficacy, with improvements in functional assessments and cardiac function in BTHS.
Long-term efficacy and safety of elamipretide in patients ...
Elamipretide was associated with sustained long-term tolerability and efficacy, with improvements in functional assessments and cardiac function in BTHS.
Expanded-access use of elamipretide in a newborn with Barth ...
Data from the OLE demonstrated a marked reverse remodelling effect of the heart (greater than 40% improvement in LV volumes) in patients treated ...
4.
pure.johnshopkins.edu
pure.johnshopkins.edu/en/publications/long-term-efficacy-and-safety-of-elamipretide-in-patients-with-baLong-term efficacy and safety of elamipretide in patients ...
Results: Ten patients entered the OLE; 8 reached the week 168 visit. Elamipretide was well tolerated, with injection-site reactions being the most common ...
Elamipretide for the Treatment of Barth Syndrome
Can we conclude that elamipretide is effective for the treatment of. Barth syndrome based on the available evidence? • The advisory committee ...
215244Orig1s000 RISK ASSESSMENT and RISK ...
7 The supportive safety data from elamipretide for the treatment of PMM and age-related macular degeneration showed similar safety results to ...
Elamipretide Clinical Trials
We are investigating elamipretide in late stage clinical studies for mitochondrial diseases such as Barth Syndrome and orphan diseases with cardiomyopathy.
Unbiased Results
We believe in providing patients with all the options.
Your Data Stays Your Data
We only share your information with the clinical trials you're trying to access.
Verified Trials Only
All of our trials are run by licensed doctors, researchers, and healthcare companies.