CompletedPhase 1NCT01849003
Study of the Effect of GS-6615 in Subjects With LQT-3
Studying Congenital long QT syndrome
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
- Gilead Sciences
- Principal Investigator
- Elizabeth Layug, MDGilead Sciences
- Intervention
- GS-6615(drug)
- Enrollment
- 24 enrolled
- Eligibility
- 18-65 years · All sexes
- Timeline
- 2013 – 2014
Study locations (1)
- University of Rochester Medical Center/Strong Memorial Hospital, Rochester, New York, United States
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.
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