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Phase 2 trial of surlorian in adults with autosomal dominant RYR1-related myopathy

2025-522343-18-00Phase 2Authorised

Sponsor
RyCarma Therapeutics
Start
Jun 2026
Modality
Small Molecules
Countries
5
01

Overview

Phase 2, randomised, double-blind trial in ryanodine receptor 1 related myopathy (RYR1-RD) comparing Surlorian with Placebo (2 arms). Primary endpoint: Change from Day 1 in 1-MSST after approximately 28 days. Planned start Jun 2026; status: authorised.

02

Drugs

Surlorian
03

Conditions

ryanodine receptor 1 related myopathy (RYR1-RD)

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