TerminatedPHASE1, PHASE2NCT05906732
Study of LQT-1213 on QTc-induced Prolongation in Healthy Adult Subjects (Part1) and on Congenital Long QT in Patients Diagnosed With Type 2 or 3 Long QT Syndrome (Part 2).
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
- Thryv Therapeutics, Inc.
- Principal Investigator
- Jan Matousek, DOSpaulding Clinical Research LLC
- Intervention
- LQT-1213(drug)
- Enrollment
- 42 enrolled
- Eligibility
- 18-60 years · All sexes
- Timeline
- 2023 – 2024
Study locations (1)
- Spaulding Clinical Research, LLC, West Bend, Wisconsin, 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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