LANDOUZY-DEJERINE MUSCULAR DYSTROPHY

Clinical trials for LANDOUZY-DEJERINE MUSCULAR DYSTROPHY explained in plain language.

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Breakthrough drug trial offers hope for rare muscle disease

Disease control Recruiting now

This study is testing an experimental drug called AOC 1020 for people with facioscapulohumeral muscular dystrophy (FSHD), a genetic condition that causes progressive muscle weakness. About 200 participants will receive either the drug or a placebo via IV infusion every six weeks …

Matched conditions: LANDOUZY-DEJERINE MUSCULAR DYSTROPHY

Phase: PHASE3 • Sponsor: Avidity Biosciences, Inc. • Aim: Disease control

Last updated Mar 30, 2026 14:32 UTC

LANDOUZY-DEJERINE MUSCULAR DYSTROPHY

Get alerted when new LANDOUZY-DEJERINE MUSCULAR DYSTROPHY trials appear

Breakthrough drug trial offers hope for rare muscle disease