5
Participants
Start Date
January 1, 2025
Primary Completion Date
January 1, 2026
Study Completion Date
January 1, 2027
Progerinin
"This is a Phase 2, open-label study to evaluate the safety and Tolerability of Progerinin for the treatment of BMD Bone Mineral Density (BMD) Loss in Subjects with Typical Werner Syndrome.~. There will be up to 5 subjects that will receive treatment with Progerinin twice daily for approximately 1 year. This study will have three phases: Screening Phase, Treatment Phase, and Follow-Up Phase."
Lead Sponsor
PRG Science & Technology Co., Ltd.
INDUSTRY