RecruitingPhase 1NCT06164730
A Study of VERVE-102 in Patients With Familial Hypercholesterolemia or Premature Coronary Artery Disease
Studying Rare hypercholesterolemia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Verve Therapeutics, Inc.
- Intervention
- VERVE-102(drug)
- Enrollment
- 85 enrolled
- Eligibility
- 18-70 years · All sexes
- Timeline
- 2024 – 2027
Study locations (21)
- Clinical Study Center, Dothan, Alabama, United States
- Clinical Study Center, Pomona, California, United States
- Clinical Study Center, Boca Raton, Florida, United States
- Clinical Study Center, Winter Park, Florida, United States
- Clinical Study Center, High Point, North Carolina, United States
- Clinical Study Center, DeSoto, Texas, United States
- Clinical Study Center, Renton, Washington, United States
- Clinical Study Center, Adelaide, Australia
- Clinical Study Center, Melbourne, Australia
- Clinical Study Center, Sydney, Australia
- Clinical Study Center, Chicoutimi, Canada
- Clinical Study Center, Montreal, Canada
- Clinical Study Center, Toronto, Canada
- Clinical Study Center, Vancouver, Canada
- Clinical Study Center, Rehovot, Israel
- +6 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT06164730 on ClinicalTrials.govOther trials for Rare hypercholesterolemia
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