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Mitochondrial Diseases clinical trials

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NCT ID: NCT02544217 Completed - Clinical trials for Mitochondrial Disease

A Dose-escalating Clinical Trial With KH176

Start date: May 2015
Phase: Phase 1
Study type: Interventional

Mitochondrial Diseases are rare progressive, multi-system, often early fatal disorders affecting both children and adults. KH176 is a novel chemical entity currently under development for the treatment of inherited mitochondrial diseases, including MELAS (Mitochondrial Encephalomyopathy, Lactic acidosis, and Stroke-like episodes), Leigh's Disease and Leber's Hereditary Optic Neuropathy (LHON). KH176 is a potent intracellular redox modulating agent targeting the reactive oxygen species which are important in the pathogenesis of disorders of mitochondrial oxidative phosphorylation. After demonstrating a favourable safety profile in the pre-clinical testing, the safety, tolerability and pharmacokinetic and pharmacodynamic characteristics of the compound will now be evaluated in healthy male subjects in this trial

NCT ID: NCT02500628 Completed - Clinical trials for Diabetes Mellitus, Type 2

Heart Rate Variability in Response to Metformin Challenge

Start date: July 2015
Phase: Phase 2
Study type: Interventional

Diseases caused by brain energy supply defects can be innate (fibromyalgia secondary to familial mitochondrial disorders) or acquired (tardive dyskinesia or weight gain associated with prolonged antipsychotic use). Patients with these possible mitochondrial disorders will provide a baseline resting heart rate sample, ingest low-dose metformin (500 mg), and then provide an additional sample 2 hours later.

NCT ID: NCT02473445 Terminated - Clinical trials for Mitochondrial Diseases

A Long-term Extension of Study RP103-MITO-001 (NCT02023866) to Assess Cysteamine Bitartrate Delayed-release Capsules (RP103) in Children With Inherited Mitochondrial Disease

Start date: May 19, 2015
Phase: Phase 2
Study type: Interventional

A long-term extension study to assess the safety, tolerability and efficacy of cysteamine bitartrate delayed-release capsules (RP103) in children with inherited mitochondrial diseases who previously enrolled into study RP103-MITO-001 (NCT02023866).

NCT ID: NCT02398201 Completed - Clinical trials for Mitochondrial Diseases

A Study of Bezafibrate in Mitochondrial Myopathy

Start date: September 2015
Phase: Phase 2
Study type: Interventional

The purpose of this study is to gather preliminary data on whether bezafibrate can improve cellular energy production in mitochondrial disease. Mitochondrial diseases are rare inherited disorders that arise due to deficient energy production within the cells of the body. Consequently, the typical clinical features arise in organs with high energy requirements. Mitochondrial disorders exhibit highly variable clinical effects, both between individuals and within families. Characteristic symptoms include muscle weakness (myopathy), hearing loss, migraine, epilepsy and stroke like episodes in addition to diabetes and heart problems. Mitochondrial disorders can therefore impact considerably on both quality of life and life expectancy. Despite this, no proven disease modifying treatments are available. Pre-clinical studies have identified that several existing medications improve mitochondrial function. Of these, bezafibrate has the best supportive data and, because it is already licensed as a treatment for high blood fats, has a well characterised side effect profile. The investigators will therefore conduct a feasibility study of bezafibrate in people with mitochondrial myopathy. Ten affected participants will be recruited and will receive a titrating course of bezafibrate three times daily for 12 weeks.

NCT ID: NCT02375438 Completed - Clinical trials for Mitochondrial Diseases

Nutritional Assessment in Mitochondrial Cytopathy

NAMITO
Start date: December 2014
Phase: N/A
Study type: Observational

The aim of this study is to assess nutritional intake (quantitatively and qualitatively), nutritional state and body composition of patients suffering from mitochondrial cytopathy, compared to healthy controls. The energy intake will be calculated through dietary protocols, the energy expenditure by indirect calorimetry and body composition will be performed with bio-impedance analysis. Further on, the investigators expect to be able to provide nutritional counselling to this population in order to increase energy and protein intake, which may improve health and well-being.

NCT ID: NCT02367014 Completed - Clinical trials for Mitochondrial Myopathy

Safety, Tolerability, and Efficacy of MTP-131 for the Treatment of Mitochondrial Myopathy

MMPOWER
Start date: February 2015
Phase: Phase 1/Phase 2
Study type: Interventional

Phase 1/2, multi-center, randomized, double-blind, multiple ascending dose, placebo-controlled study that enrolled 36 subjects with mitochondrial myopathy associated with genetically confirmed mitochondrial disease to evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary efficacy of MTP-131 in this patient population.

NCT ID: NCT02348125 Recruiting - Clinical trials for Autism Spectrum Disorders

Does Clinical Treatment of Mitochondrial Dysfunction Impact Autism Spectrum Disorder (ASD)?

MitoASD
Start date: March 2016
Phase: Phase 1
Study type: Interventional

In this study, 50 children between 3 and 12 years old with formally diagnosed autistic spectrum disorders (ASD) and also having significant mitochondrial dysfunction will be treated for a 3 month period with the Mitochondrial Cocktail, a combination of specific nutritional supplements and metabolite intermediates (including anti-oxidants) and bio-energy substrates. A series of neurological and psychological evaluations will be conducted by trained evaluators/clinicians to evaluate both the severity and the clinical presentation of the ASD/mitochondrial dysfunction with each subject at baseline prior to treatment, after the 3 month treatment and again at 6 months, after another 3 month non-treatment period. In addition, laboratory investigations will be conducted at the same time-points to assess the mitochondrial dysfunction and cellular biomarkers thought to be associated with autistic and mitochondrial disorders. These investigations will include the analysis of samples of blood and cheek/buccal swabs collected from each child to assess select biochemical markers of ASD. The Mitochondrial Cocktail treatment will be administered at home once a day continuously for a total of 3 months. All the children in the study will be treated with the same Mitochondrial Cocktail (an open label study).

NCT ID: NCT02327364 Completed - Pearson Syndrome Clinical Trials

Natural History of Pearson Syndrome

Start date: March 2014
Phase:
Study type: Observational [Patient Registry]

The purpose of this 3-year, multi-site, non-randomized, prospective, observational study is to characterize the natural history of Pearson Syndrome. The Syndrome is a rare mitochondrial disorder due to a large-scale mtDNA deletion. Children typically present in their 1st two years of life (most in infancy) with anemia and/or pancreatitis. Most individuals with Pearson Syndrome die in childhood. Those who survive evolve to Kearns-Sayre Syndrome/Chronic Progressive External Ophthalmoplegia (KSS/CPEO) although accurate survival estimates are not yet known.

NCT ID: NCT02311257 Completed - Clinical trials for Mitochondrial Disease

Survey on Supplement Use in Mitochondrial Disease

Start date: September 2014
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to learn about the use of nutritional supplements in patients with mitochondrial disease.

NCT ID: NCT02286856 Completed - Clinical trials for Mitochondrial Disorders

DINAMITE Study Nutritional State and Effect Diet in Mitochondrial Disease

DINAMITE
Start date: March 2014
Phase: N/A
Study type: Interventional

The m.3243A>G mutation is the most frequent cause of mitochondrial disease in adults, for which currently no therapy is available and treatment is solely supportive. Since both malnutrition and obesity are frequently seen in these patients, an adequate nutritional intervention to improve body composition and function might improve the quality of life of these patients. Hypothesis / research questions Hypothesis part 1: Patients with mitochondrial disorders caused by the m.3243 A>G mutation have an increased risk for malnutrition. Hypothesis part 2 : Intervention study: Dietary intervention in adults with a mitochondrial disorder caused by the m.3243 A>G mutation has a positive effect on nutritional status, activity, hand grip strength, body composition, food intake, fatigue and quality of life.