Emergency Use Protocol for EPI-743 in Acutely Ill Patients With Inherited Mitochondrial Respiratory Chain Disease Within 90 Days of End-of-Life Care
| Registry | NCT01370447 |
|---|---|
| Status | No longer available |
| Study type | Expanded access |
| Sponsor | PTC Therapeutics (Industry) |
| Conditions | Mitochondrial Diseases |
| Interventions | EPI-743 (Drug) |
| Dates | first posted 2011-06-10, last updated 2024-01-23 |
| Locations | 16 sites in United States |
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All trials for Mitochondrial Diseases All trials of EPI-743
This study will evaluate the safety and efficacy of EPI-743 in participants with severe mitochondrial respiratory chain diseases who are considered to be within 90 days of end-of-life care.
Sex: All, ages: 1 Year to any
Inclusion criteria: 1. Participants with genetic diagnosis: Genetically confirmed diagnosis of Inherited mitochondrial respiratory chain disease 2. Participants with clinical diagnosis: Diagnosis of inherited mitochondrial disease absent genetic confirmation; Specifically, participants must meet the diagnostic criteria of "definite" or "probable" mitochondrial disease as defined by Bernier et al., 2002 3. Deemed by principal investigator to be within 90 days of end-of-life hospice/terminal care 4. Male or female age > one year 5. Hematocrit within normal range for age group 6. Agreement to use contraception if within reproductive years 7. Participant or participant's guardian able to consent and comply with protocol requirements 8. Presence of caregiver to ensure study compliance 9. Abstention from use of all pill-form dietary supplements and non-prescribed medications (except as allowed by the investigator) 10. Abstention from foods or beverages or bars fortified with Coenzyme Q10, vitamin E, super-fortified "functional" foods or beverages 11. Abstention from use of idebenone 12. Clinically staged with a Mitochondrial Disease Scale such as the Newcastle Score Exclusion criteria: 1. Allergy to EPI-743, vitamin E or sesame oil 2. Clinical history of bleeding or abnormal prothrombin time (PT)/partial thromboplastin time (PTT) (excluding anticoagulation Rx) 3. Hepatic insufficiency with liver function tests (LFTs) greater than two times normal 4. Renal insufficiency requiring dialysis 5. Fat malabsorption syndromes precluding drug absorption 6. Any other concurrent inborn errors of metabolism 7. Severe end-organ hypo-perfusion syndrome secondary to cardiac failure resulting in lactic acidosis 8. Pregnancy
| Facility | City | Country | Status |
|---|---|---|---|
| UCLA | Los Angeles, California | United States | |
| CHOC Children's Clinic | Orange, California | United States | |
| Lucille Packard Children's Hospital | Palo Alto, California | United States | |
| UCSD | San Diego, California | United States | |
| Stanford Children's Health | Stanford, California | United States | |
| Emory University | Decatur, Georgia | United States | |
| CUMC (Columbia University) | New York, New York | United States | |
| Carolinas Medical Center | Charlotte, North Carolina | United States | |
| Akron Children's Hospital | Akron, Ohio | United States | |
| Cleveland Clinic | Cleveland, Ohio | United States | |
| Children's Hospital of Philadelphia | Philadelphia, Pennsylvania | United States | |
| MUSC | North Charleston, South Carolina | United States | |
| Baylor College of Medicine | Houston, Texas | United States | |
| UTH | Houston, Texas | United States | |
| Naval Hospital, Bremerton | Bremerton, Washington | United States | |
| Seattle Children's Hospital | Seattle, Washington | United States |