Trial record 2 of 5 for:    "Leigh syndrome"

Open-Label, Dose-Escalating Study to Assess Safety, Tolerability, Efficacy, PK and PD of RP103 in Children With Inherited Mitochondrial Disease (RP103-MITO-001)

This study is currently recruiting participants. (see Contacts and Locations)
Verified July 2014 by Raptor Pharmaceuticals Inc.
Sponsor:
Information provided by (Responsible Party):
Raptor Pharmaceuticals Inc.
ClinicalTrials.gov Identifier:
NCT02023866
First received: December 17, 2013
Last updated: July 2, 2014
Last verified: July 2014
  Purpose

Patients (male or female) with either documented genetically confirmed diagnosis of inherited mitochondrial diseases, who are ≥ 2 years old and < 18 years, and meet other specified inclusion and exclusion criteria, will be included in this study.

Patients with inherited mitochondrial diseases associated with nuclear or mitochondrial DNA mutations that impair the respiratory chain. These include, but are not limited to the following clinical syndromes: Leber's hereditary optic neuropathy; myoclonic epilepsy and ragged-red fibers (MERFF); mitochondrial encephalomyopathy, lactic acidosis, and stroke-like syndrome (MELAS); Kearn-Sayre syndrome; subacute necrotizing encephalopathy (Leigh Syndrome); POLG-related disorders (Alpers-Huttenlocher Syndrome, Autosomal Dominant Progressive External Ophthalmoplegia, Autosomal Recessive Progressive External Ophthalmoplegia, Childhood Myocerebrohepatopathy Spectrum Disorders, Myoclonic Epilepsy Myopathy Sensory Ataxia, POLG-Related Ataxia Neuropathy Spectrum Disorders); Mitochondrial neurogastrointestinal encephalopathy syndrome (MNGIE), also called myoneurogastrointestinal encephalopathy syndrome or POLIP syndrome; others, e.g., mitochondrial cardiomyopathies and other syndromes due to multiple mitochondrial DNA deletions.

Screening eligibility criteria for each subject will be reviewed by participating Investigators and Raptor's medical officer, in an attempt An effort to ensure at least 2/3 of the enrolled subjects have Leigh Syndrome (i.e., patients with Leigh Syndrome clinical presentation, genetically confirmed by known Leigh Syndrome mutations and no variants of uncertain significance).

Initially, up to 32 patients will be enrolled if there is no toxicity up to the level of 1.3 g/m2/day of RP103. After the two interim analyses planned to occur after 12 and then 24 subjects complete Week 24, sample size may be decreased to 24 or increased to a maximum of 64 subjects.

The rationale for choosing patients with inherited mitochondrial disease who are age 2 and older is based on available clinical data collected in previous and current RP103 studies in other indications, in subjects aged 2 years and older.


Condition Intervention Phase
Inherited Mitochondrial Disease, Including Leigh Syndrome
Drug: Cysteamine Bitartrate Delayed-release Capsules (RP103)
Phase 2
Phase 3

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Open-Label, Dose-Escalating Study to Assess Safety, Tolerability, Efficacy, Pharmacokinetics and Pharmacodynamics of Cysteamine Bitartrate Delayed-release Capsules (RP103) in Children With Inherited Mitochondrial Disease

Resource links provided by NLM:


Further study details as provided by Raptor Pharmaceuticals Inc.:

Primary Outcome Measures:
  • Change in Newcastle Paediatric Mitochondrial Disease Scale (NPMDS) Score [ Time Frame: Baseline vs. Week 24 ] [ Designated as safety issue: No ]
    Quality of life


Secondary Outcome Measures:
  • Change over time in Pharmacodynamic Biomarkers [ Time Frame: Baseline and Weeks 4, 8, 12, 16, 20, 24 ] [ Designated as safety issue: No ]
    glutathione, acetoacetate, beta-hydroxybutyrate, lactate


Estimated Enrollment: 32
Study Start Date: April 2014
Estimated Study Completion Date: June 2015
Estimated Primary Completion Date: January 2015 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: RP103 Drug: Cysteamine Bitartrate Delayed-release Capsules (RP103)

  Eligibility

Ages Eligible for Study:   2 Years to 17 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Age ≥ 2 years and < 18 years
  2. Body weight ≥ 5 kgs
  3. Documented (genetically confirmed known mutation, i.e. no variants of uncertain significance) diagnosis of inherited mitochondrial disease other than Friedreich's ataxia (FRDA)
  4. Moderate disease severity based on Newcastle Pediatric Mitochondrial Disease Scale (NPMD) score, with a score between 15 to 45 inclusive
  5. For patients regularly taking dietary supplements such as creatinine, alpha-lipoic acid, CoQ10, vitamin B, carnitine, etc. they have to have been taking them for at least 3 months pre-study and will agree to keep these the same throughout the study (from the Screening Visit to Study Exit)
  6. Willing to abstain from initiating dietary supplements and non-prescribed medications, except as allowed by the Investigator, throughout the study
  7. Willing and able to comply with study drug dosing requirements, i.e. ingest the RP103 capsules intact, or sprinkled in liquid or soft food, or using a g-tube
  8. Sexually active female subjects of childbearing potential (i.e., not surgically sterile [tubal ligation, hysterectomy, or bilateral oophorectomy]) must agree to utilize two of the following acceptable forms of contraception throughout the study (from the Screening Visit to Study Exit):

    1. Hormonal contraception: birth control pills, injection, patch, vaginal ring or implant;
    2. Condom or diaphragm, with spermicide;
    3. Intrauterine device (IUD)
    4. Sterile male partner (vasectomy performed at least 6 months prior to the study).
  9. Patient's legally authorized representative must provide written informed consent; Patient must provide assent, if required by local/institutional requirements

Exclusion Criteria:

  1. Documented diagnosis of concurrent inborn errors of metabolism
  2. Non-elective hospitalization relative to mitochondrial disease or direct complication of disease within 60 days prior to the Screening Visit.
  3. Platelet count, lymphocyte count or hemoglobin below the lower limit of normal (LLN) at the Screening Visit
  4. Hepatic insufficiency with liver enzyme tests (alkaline phosphatase, AST or ALT) greater than 2.5 times the upper limit of normal (ULN) at the Screening Visit
  5. Bilirubin > 1.2 g/dl at the Screening Visit
  6. Inability to complete the elements of the study, e.g., coma, hemodynamic instability or ventilator.
  7. Malabsorption requiring TPN, chronic diarrhea, bouts of pseudo obstruction
  8. Severe end-organ hypo-perfusion syndrome secondary to cardiac failure resulting in lactic acidosis
  9. Patients with suspected elevated intracranial pressure, pseudotumor cerebri (PTC) and/or papilledema
  10. Severe gastrointestinal disease including gastroparesis
  11. History of angina, myocardial infarction, or cardiac surgery within 2 years prior to the Screening Visit
  12. Any clinically significant ECG, including dysrhythmia, or clinically significant abnormal laboratory finding not already listed above at the Screening Visit
  13. History of drug or alcohol abuse
  14. History of pancreatitis
  15. Participated in an investigational drug trial within 30 days or, within 90 days for a biologic, device, or surgical treatment, for inherited mitochondrial diseases prior to the Screening Visit
  16. Known or suspected hypersensitivity to cysteamine and penicillamine
  17. Female subjects who are nursing, planning a pregnancy, known or suspected to be pregnant, or with a positive serum pregnancy test at the Screening Visit
  18. Patients who, in the opinion of the Investigator, are not able or willing to comply with the protocol
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT02023866

Contacts
Contact: Kenny Jones PhD, Raptor Clinical Operations 415-408-6283 kjones@raptorpharma.com

Locations
United States, California
University of California at San Diego (UCSD) Not yet recruiting
San Diego, California, United States
Contact: Richard Haas, MD    858-822-6700    rhaas@ucsd.edu   
Contact: Gail Reiner, FNP, PhD    (619) 471-9134    gereiner@ucsd.edu   
Principal Investigator: Richard Haas, MD         
Stanford University Not yet recruiting
Stanford, California, United States
Contact: Gregory Enns, MB, ChB    650-498-5798    greg.enns@stanford.edu   
Principal Investigator: Gregory Enns, MB, ChB         
United States, Ohio
Akron Children's Hospital Recruiting
Akron, Ohio, United States
Contact: Bruce Cohen, MD    330-543-8050    bcohen@chmca.org   
Contact: Hilary Tonni    (330) 543-4734    htonni@chmca.org   
Principal Investigator: Bruce Cohen, MD         
United States, Texas
Baylor College of Medicine Recruiting
Houston, Texas, United States
Contact: Fernando Scaglia, MD    832-822-4280    fscaglia@bcm.edu   
Contact: Dianne X Dang, Clinical Research Coordinator    832-822-4283    diannen@bcm.edu   
Principal Investigator: Fernando Scaglia, MD, FACMG         
Sponsors and Collaborators
Raptor Pharmaceuticals Inc.
Investigators
Principal Investigator: Bruce H. Cohen, MD Akron Children's Hospital
  More Information

Additional Information:
Publications:
Responsible Party: Raptor Pharmaceuticals Inc.
ClinicalTrials.gov Identifier: NCT02023866     History of Changes
Other Study ID Numbers: RP103-MITO-001
Study First Received: December 17, 2013
Last Updated: July 2, 2014
Health Authority: United States: Food and Drug Administration

Keywords provided by Raptor Pharmaceuticals Inc.:
subacute necrotizing encephalopathy (Leigh Syndrome);
Leber's hereditary optic neuropathy;
myoclonic epilepsy and ragged-red fibers (MERFF);
mitochondrial encephalomyopathy, lactic acidosis, and stroke-like syndrome (MELAS);
Kearn-Sayre syndrome;
POLG-related disorders;
Mitochondrial neurogastrointestinal encephalopathy syndrome (MNGIE)

Additional relevant MeSH terms:
Leigh Disease
Mitochondrial Diseases
Brain Diseases, Metabolic, Inborn
Brain Diseases, Metabolic
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Metabolism, Inborn Errors
Genetic Diseases, Inborn
Pyruvate Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Metabolic Diseases
Cysteamine
Radiation-Protective Agents
Protective Agents
Physiological Effects of Drugs
Pharmacologic Actions

ClinicalTrials.gov processed this record on August 18, 2014