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Clinical trial

A Randomized, Double-blind, Placebo-controlled, Phase 1/2 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Exploratory Efficacy of AOC 1020 Administered Intravenously to Participants With Facioscapulohumeral Muscular Dystrophy (FSHD)

NCT05747924 is registered in ClinicalTrials.gov with Avidity Biosciences, Inc. as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Randomized, Double-blind, Placebo-controlled, Phase 1/2 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Exploratory Efficacy of AOC 1020 Administered Intravenously to Participants With Facioscapulohumeral Muscular Dystrophy (FSHD)
Lead sponsor
Avidity Biosciences, Inc.
Phase
Phase 1/2
Overall status
Completed
Start date
April 4, 2023
Completion date
March 20, 2026
Enrollment
90 (actual)
Sites
17

Conditions

As the registry lists them; a condition with its own page is linked.

atrophies, facioscapulohumeral, atrophy, facioscapulohumeral, dystrophies, facioscapulohumeral muscular, dystrophies, landouzy-dejerine, dystrophy, facioscapulohumeral muscular, dystrophy, landouzy-dejerine, facio-scapulo-humeral dystrophy, facioscapulohumeral atrophy, facioscapulohumeral muscular dystrophy 1, facioscapulohumeral muscular dystrophy 2, fascioscapulohumeral muscular dystrophy, fascioscapulohumeral muscular dystrophy type 1, fascioscapulohumeral muscular dystrophy type 2, fmd, fmd2, fsh, fsh muscular dystrophy, fshd, fshd1, fshd2, landouzy dejerine dystrophy, landouzy-dejerine muscular dystrophy, landouzy-dejerine syndrome, muscular dystrophies, muscular dystrophy, facioscapulohumeral, muscular dystrophy, landouzy dejerine, progressive muscular dystrophy