CLINICAL_TRIALS
ClinicalTrials.gov record update
A Randomized, Double-blind, Placebo-controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Intravenous AOC 1020 for the Treatment of Facioscapulohumeral Muscular Dystrophy (FSHD)
This page presents selected fields from the linked source record. It does not add a medical interpretation.
Record identity and dates
- Source
- ClinicalTrials.gov
- Source record ID
- NCT07038200
- Title field or adapter rule
- protocolSection.identificationModule.officialTitle
- Ingested At
- 2026-04-25T22:28:36.508433+00:00
- Published At
- 2026-01-20T00:00:00+00:00
- Record Updated At
- 2026-01-20
- Timestamp Basis
- source retrieval time was not retained by the feed adapter
- Date limitation
- source retrieval time was not retained by the feed adapter
Fields recorded by this source
- protocolSection.conditionsModule.conditions
["Facioscapulohumeral Muscular Dystrophy", "FSHD", "FSHD - Facioscapulohumeral Muscular Dystrophy", "FSHD1", "FSHD2", "Fascioscapulohumeral Muscular Dystrophy", "Fascioscapulohumeral Muscular Dystrophy Type 1", "Fascioscapulohumeral Muscular Dystrophy Type 2", "Facioscapulohumeral Muscular Dystrophy 1", "Facioscapulohumeral Dystrophy", "Facio-Scapulo-Humeral Dystrophy", "Facioscapulohumeral Muscular Dystrophy 2", "Facioscapulohumeral Muscular Dystrophy Type 1 (FSHD1)", "FSH Muscular Dystrophy", "Landouzy Dejerine Dystrophy", "Landouzy-Dejerine Muscular Dystrophy", "Landouzy-Dejerine Syndrome"]- protocolSection.statusModule.lastUpdatePostDateStruct.date
"2026-01-20"- protocolSection.identificationModule.nctId
"NCT07038200"- protocolSection.identificationModule.officialTitle
"A Randomized, Double-blind, Placebo-controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Intravenous AOC 1020 for the Treatment of Facioscapulohumeral Muscular Dystrophy (FSHD)"- protocolSection.statusModule.overallStatus
"RECRUITING"- protocolSection.designModule.phases
["PHASE3"]- protocolSection.statusModule.resultsFirstPostDateStruct.date
""
Study condition terms
Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.
This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.