Phase 2, Open-Label Study to Evaluate the Safety and Tolerability of Progerinin in Werner Syndrome

PHASE2Not yet recruitingINTERVENTIONAL
Enrollment

5

Participants

Timeline

Start Date

January 1, 2025

Primary Completion Date

January 1, 2026

Study Completion Date

January 1, 2027

Conditions
Werner Syndrome
Interventions
DRUG

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."

All Listed Sponsors
lead

PRG Science & Technology Co., Ltd.

INDUSTRY