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RecruitingPhase 2/Phase 3

Study to Evaluate the Pharmacodynamics, Safety and Efficacy of SKY-0515 in Participants With Huntington's Disease

Skyhawk Therapeutics, Inc. · NCT07378644

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 25+ · All sexes
Healthy volunteers
Not accepted (a condition is required)
Study type
Interventional · Phase 2, Phase 3
Target enrollment
400
US sites recruiting
1
Study start
January 6, 2026
Record last updated
October 16, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

The goal of this clinical trial is to test if the drug SKY-0515, an oral medication, can lower harmful proteins linked to Huntington's Disease (HD) and improve the symptoms of participants with HD. This study includes men and women aged 25 and older who have HD confirmed by genetic testing and meet certain requirements for physical ability and independence.

Being studied: SKY-0515; SKY-0515 Placebo

Conditions: Huntington Disease

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • 25 years or older.
  • Huntington's Disease confirmed through genetic testing, with a specific change in exon 1 of the HTT gene (CAG repeat of 40 or more).
  • Total Functional Capacity (TFC) score of 10 or more).
  • Total Motor Score (TMS) of 6 or more).
  • Independence Score (IS) of 70 or more).
  • Women who can have children must have a negative pregnancy test before starting and use two types of birth control during the study and for 30 days after the last dose of the study drug.
  • Men must agree to use birth control during the study and for 90 days after the last dose.
  • Agree to sign a consent form and follow the study's rules and schedule.

Exclusion Criteria

  • Other Serious health problems or brain/spinal issues that could interfere with the study or make procedures unsafe.
  • Conditions that interfere with protocol-specified assessments, like an implanted medical device or difficulty getting an MRI.
  • Cancer, except for some types of skin cancer, or a history of cancer in the last five years.
  • Severe allergies or have reacted badly to similar drugs in the past.
  • Taking medications or treatments that might interfere with the study.
  • Participated in another study or taken experimental drugs in the last two months (or longer for some drugs).
  • Any kind of gene therapy.
  • History of suicidal thoughts, severe depression, or have attempted suicide in the past year.
  • Liver function tests show significant abnormalities.
  • Positive for hepatitis B, hepatitis C, or HIV.
  • Pregnancy, breastfeeding, or planning to become pregnant during the study.

Recruiting US locations

  • CenExel Denver CO

    Englewood, CO 80113

    Site contact: Liza Heap · +1 303 762 6674 · e.heap@cenexel.com

Study contacts (from the official record)

  • Study Director, MD · 6178580041 · sky0515trials@skyhawktx.com
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Study to Evaluate the Pharmacodynamics, Safety and Efficacy of… (NCT07378644) | Bored Studies