An Open-label Study to Investigate ECUR-506 in Male Babies Less Than 9 Months of Age With Neonatal Onset OTC Deficiency

a study on Ornithine Transcarbamylase Deficiency Urea Cycle Disorders, Inborn Liver Disease Metabolic Disease

Summary

Eligibility
for males ages up to 7 months (full criteria)
Location
at UCLA
Dates
study started
study ends around

Description

Summary

Ornithine Transcarbamylase (OTC) deficiency, the most common urea cycle disorder, is an inherited metabolic disorder caused by a genetic defect in a liver enzyme responsible for detoxifying of ammonia. Individuals with OTC deficiency can develop elevated levels of ammonia in the blood, potentially resulting in severe consequences, including cumulative and irreversible neurological damage, coma, and death. The most severe form presents shortly after birth and occurs more commonly in boys than girls.

This is a Phase 1/2/3, open-label, multicenter study evaluating the safety, efficacy, and dose of ECUR-506 in male babies with neonatal-onset OTC deficiency. The primary objective is to evaluate the safety, tolerability, and efficacy of up to three dose levels of ECUR-506 following intravenous (IV) administration of a single dose.

Official Title

A Phase 1/2/3 First-in-Human, Open-Label, Dose-Escalation Study to Evaluate the Safety and Efficacy of a Single Intravenous (IV) Administration of ECUR-506 in Males Less Than 9 Months of Age With Genetically Confirmed Neonatal Onset Ornithine Transcarbamylase (OTC) Deficiency

Details

The study drug, ECUR-506, is an investigational gene editing therapy. Gene editing is an approach used to repair, replace, or introduce functional copies of genes that are not working properly. ECUR-506 contains a functional copy of the OTC gene, along with a gene to encode an editing enzyme that enables insertion of the OTC gene into the genome. The study drug is administered as a single IV infusion. Because genes cannot enter cells on their own, ECUR-506 uses a delivery system based on adeno-associated virus (AAV), a commonly used viral vector, to transport the genetic material into cells.

Keywords

Ornithine Transcarbamylase Deficiency, Ornithine Transcarbamylase Deficiency Disease, Ornithine Carbamoyltransferase Deficiency (Disorder), Urea Cycle Disorders, Inborn, Amino Acid Metabolism, Inborn Errors, Ammonia, Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Central Nervous System Diseases, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, High Ammonia, Hyperammonemia, Inborn, Inborn Errors, Inherited Metabolic Disorders, Liver Disease, Liver Transplant, Metabolism, Metabolic Diseases, Metabolism, Inborn Errors, Neonatal, Nervous System Diseases, Neurometabolic disorders, NH4, Ornithine, OTC, OTC Deficiency, OTCD, Transcarbamylase, UCD, Urea Cycle Disorders, X-Linked, Ornithine Carbamoyltransferase Deficiency Disease, Inborn Urea Cycle Disorders, Inborn Errors Amino Acid Metabolism, Metabolic Brain Diseases, Inborn Genetic Diseases, X-Linked Genetic Diseases, Liver Diseases, Inborn Errors Metabolism, ECUR-506

Eligibility

You can join if…

Open to males ages up to 7 months

  1. Male sex
  2. Gestational or adjusted (corrected) gestational age ≥ 37 weeks
  3. Age at screening is 24 hours to 7 months
  4. Weight ≥ 3.5 kg and ≤ 13.5 kg at screening
  5. Has received age-appropriate vaccinations
  6. Genetically confirmed OTCD defined by genetic confirmation of an OTC variant (pathogenic or likely pathogenic) associated with severe neonatal OTCD defined below in Inclusion Criteria #7 or has the same OTC variant as a family member who had severe neonatal OTCD within first week of life.
  7. Severe neonatal OTCD defined by hyperammonemic crisis with elevated ammonia level of >560 μmol/L and clinical symptoms within first week of life, and currently receiving treatment with both dietary protein restriction and nitrogen scavenger therapy.
  8. Current or historical biochemical profile consistent with OTCD
  9. Participant's parent(s)/LAR must be able to comprehend and be willing to provide a signed IRB/IEC-approved ICF.

You CAN'T join if...

  1. Neonatal diagnosis of severe to profound Hypoxic Ischemic Encephalopathy due to birth injury
  2. Requiring urgent liver transplant due to liver failure as assessed by the PI.
  3. Contiguous gene deletion involving the OTC gene and including at least the CYBB gene on the telomeric side or the TSPAN7 gene on the centromeric side.
  4. Known or suspected major organ injury/dysfunction/anomalies.
  5. Vital sign and laboratory abnormalities outside of reference ranges.
  6. Treatment with any other gene therapy or gene editing therapy
  7. Co-enrollment in any other study unless approved by the sponsor.
  8. Any condition, that in the opinion of the Investigator, would compromise the safety of the participant or study data
  9. Documented vertical transmission of HepA/HepB/HepC
  10. Documented in-utero teratogen, substance, and/or alcohol exposure, which in the opinion of the Investigator may increase the participant's risk of developmental delays, congenital anomalies, and/or significant medical complications

Locations

  • UCLA Mattel Children's Hospital accepting new patients
    Los Angeles California 90095 United States
  • Oregon Health and Science University accepting new patients
    Portland Oregon 97239 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
iECURE, Inc.
ID
NCT06255782
Phase
Phase 1/2 research study
Study Type
Interventional
Participants
Expecting 20 study participants
Last Updated
Contact us about this trial