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Safety and Tolerability of S 48168 (ARM 210) for the Treatment of RYR1-related Myopathies (RYR1-RM)

Trial Profile

Safety and Tolerability of S 48168 (ARM 210) for the Treatment of RYR1-related Myopathies (RYR1-RM)

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 23 Apr 2024

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At a glance

  • Drugs ARM 210 (Primary)
  • Indications Congenital structural myopathies
  • Focus Adverse reactions
  • Acronyms RYR1-RM
  • Sponsors ARMGO Pharma
  • Most Recent Events

    • 18 Apr 2024 Status changed from active, no longer recruiting to completed.
    • 30 Jan 2024 According to ARMGO Pharma media release, the data from this study published in the peer reviewed Journal eClinicalMedicine, part of the Lancet family of publications.
    • 29 Jan 2024 Results ARMGO Pharma published in the Media Release

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