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Study identifier: NCT06805695 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Long-term Follow-up (LTFU) Study of Participants in Any iECURE Protocol Using an Investigational Product (IP)

Condition: Ornithine Transcarbamylase Deficiency · Ornithine Transcarbamylase Deficiency Disease · Urea Cycle Disorders, Inborn  ·  Sponsor: iECURE, Inc.

PhaseN/A
Planned participants13
Who can joinAll sexes, 7 Months to 15 Months
Healthy volunteersNo

About this study

This LTFU is being conducted to assess long-term safety and durability of response in participants dosed with IP in a parent protocol, and to collect longitudinal natural history in enrolled but not dosed participants who also participated in a parent protocol.

This description comes directly from the study's public registry record.

Talk to the study team

George Diaz, M.D., Ph.D.  ·  1-877-694-3558  ·  medinfo@iecure.com

Always discuss trial participation with your own doctor first.

Locations (1)

Great Ormond Street HospitalLondon, United KingdomRecruiting

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Source record: clinicaltrials.gov/study/NCT06805695