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A Phase 2, Open-Label Study to Evaluate the Safety and Tolerability of Progerinin for the Treatment of Bone Mineral Density (BMD) Loss in Subjects With Typical Werner Syndrome

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Trial Profile

A Phase 2, Open-Label Study to Evaluate the Safety and Tolerability of Progerinin for the Treatment of Bone Mineral Density (BMD) Loss in Subjects With Typical Werner Syndrome

Status: Not yet recruiting
Phase of Trial: Phase II

Latest Information Update: 03 Feb 2026

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At a glance

  • Drugs Progerinin (Primary)
  • Indications Osteoporosis; Werner syndrome
  • Focus Adverse reactions
  • Sponsors PRG Science & Technology

Most Recent Events

  • 23 Jan 2026 Planned End Date changed from 1 Jan 2027 to 1 Dec 2027.
  • 23 Jan 2026 Planned primary completion date changed from 1 Jan 2026 to 1 Dec 2027.
  • 23 Jan 2026 Planned initiation date changed from 1 Jan 2025 to 1 Jul 2026.

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