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iMagemHTT-009- FIH Evaluation of Novel Mutant Huntingtin PET Radioligand [11C]CHDI-00491009

Study acronym: iMagemHTT-009
StatusRecruiting
PhaseEarly Phase 1
Started2026-02-24
View on ClinicalTrials.gov ↗

Amendment history

2026-03-12
notable
Not Yet Recruiting→Recruiting Study Identification, Study Status, Contacts/Locations v1
Trial statusNot Yet Recruiting→Recruiting
Primary completion date2026-05→2028-03
Completion date2026-09→2028-03
Start dateestimated 2025-03→confirmed 2026-02-24
Study sitesdetails revised at 1 of 1 site
2024-10-08
minor
Original filing
This is a FIH (first-in-human) study to evaluate the clinical utility of the radioligand \[11C\]CHDI-00491009 as a PET tracer that binds specifically to mutant huntingtin (mHTT) aggregates in Huntington's disease (HD). The study is divided into three cohorts defined by the Huntington's Disease Integrated Staging System (HD-ISS): Cohort 1 - initial tracer validation (3 healthy controls (HCs)); Cohort 2 - target validation and test-retest variability (6 HD-ISS Stage 3 participants and 6 age and biological sex-matched HCs); Cohort 3 - target sensitivity (6 HD-ISS Stage 2 participants and 6 age and biological sex-matched HCs). An interim analysis (IA) will be conducted after the completion of each cohort, followed by a final analysis for the study. In addition to imaging, exploratory biomarkers, including somatic instability index, soluble mHTT and total huntingtin (HTT), will be assessed. All participants with HD (PwHD) will have an additional blood sample drawn at the screening visit to assess the somatic instability index and will also be invited to provide an optional cerebrospinal fluid (CSF) sample for measurement of soluble mHTT and total HTT.
Trial Details
NCT Number NCT06634628
Lead Sponsor CHDI Foundation, Inc.
Collaborators: Universitaire Ziekenhuizen KU Leuven
Conditions Huntington Disease, HD, PET Tracer, Positron Emission Tomography, Radioligand, Imaging, mHTT, Huntington's +1 more
Enrollment 27 participants
Start Date 2026-02-24
Primary Completion 2028-03 (estimated)
Study Completion 2028-03 (estimated)
Updated on ClinicalTrials.gov 2026-03-13