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Frequency of Selected Single Nucleotide Polymorphisms in Huntington Disease Gene Expansion Carriers (WE45491)

Objective

ClinicalTrials.gov ID: NCT06667414
Ages Eligible: 25 to 60 Years
Sexes Eligible: All
Study Phase: Observational
Study Completion (Estimated): September 2028

Principal Investigator: Pinky Agarwal, MD, FAAN

Contact Information:

EvergreenHealth Research Department
425-899-5385
EvergreenResearch@evergreenhealthcare.org

Summary:

For participation in this epidemiological study, a single-day visit at the study site is required. Participants will be recruited from Huntington Disease clinics, and they will be asked to answer questions regarding their demographics, including sex, age, race and ethnicity, and their medical and medication history. At the end of the visit, a blood sample will be drawn to allow testing with a sequencing assay that is specifically designed for phasing single nucleotide polymorphisms (SNPs) on the wild-type Huntington (wtHTT) and mutant Huntington (mHTT) alleles.

Eligibility Criteria:

Inclusion Criteria

  • Have signed the Informed Consent Form (ICF)
  • Aged 25 to 60 years, inclusive, at the time of signing the ICF
  • Confirmation of Huntington Disease (HD) gene expansion mutation carrier status
  • Confirmation of Total Functional Capacity (TFC) ≥9 and Total Motor Score (TMS) >6 within 12 months prior to signing the ICF
  • Ability to tolerate blood draws

Exclusion Criteria

  • None

Clinical Trial Categories

  • Huntington's Disease

Location

  • EvergreenHealth Clinical Trials
    12039 NE 128th Street, Suite 300
    Kirkland, WA 98034
    Main: 425-899-5385

Contact Us

Call us at (425) 899-5385 or use our online information request form.

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