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Clinical Trial Summary

This study will collect long term follow-up data regarding overall survival and neurological parameters from patients previously identified and/or enrolled in Protocols 09-CH-0059 and 90-CH0149 and Historical Control data on Menkes disease patients.


Clinical Trial Description

Primary Objective: 1. To provide additional clinical and safety data on long term following administration of Copper Histidinate treatment in patients treated with Copper Histidinate under Protocols 09-CH-0059 and 90-CH0149 and untreated patients previously identified and/or enrolled in Protocol 09-CH-0059. 2. To provide additional Historical Control data on Menkes disease patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04337684
Study type Observational
Source Cyprium Therapeutics, Inc.
Contact
Status Enrolling by invitation
Phase
Start date December 1, 2019
Completion date December 31, 2023

See also
  Status Clinical Trial Phase
Recruiting NCT05687474 - Baby Detect : Genomic Newborn Screening
Enrolling by invitation NCT03655223 - Early Check: Expanded Screening in Newborns
Recruiting NCT04977388 - NORTHERA (DROXIDOPA) for Dysautonomia in Adult Survivors of Menkes Disease and Occipital Horn Syndrome Phase 1/Phase 2
Completed NCT00811785 - Molecular Bases of Response to Copper Treatment in Menkes Disease, Related Phenotypes, and Unexplained Copper Deficiency Phase 3
Available NCT04074512 - Copper Histidinate Treatment for Menkes Disease