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Study to Evaluate the Safety and Efficacy of PF-06939926 for the Treatment of Duchenne Muscular Dystrophy

← catalyst calendar

NCT04281485 · results posted

Sponsored by Pfizer (industry) · PFE — their whole pipeline →.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
114actual
Sites
53
Countries
Australia, Belgium, Canada +12

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2020-11-05actualWhen the study began enrolling
Primary completion2024-05-15actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2039-04-15estimatedThe whole study's end, after follow-up
First posted2020-02-24actualWhen this record first appeared on the registry
Results posted2025-06-08actualWhen the sponsor posted results to the registry
Record updated2026-07-22actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Duchenne Muscular Dystrophy

Interventions

  • Genetic: PF-06939926
  • Other: Placebo
  • Other: Placebo
  • Genetic: PF-06939926

Primary outcome

what the primary-completion date above is the date OF
Change From Baseline in North Star Ambulatory Assessment (NSAA) Total Score at Week 52
measured Baseline, Week 52

Posted documents

hosted by the registry — we link, never re-serve
Study Protocolposted 2023-12-28 · 4.1 MB · Prot_000.pdf
Statistical Analysis Planposted 2024-04-08 · 733 KB · SAP_001.pdf

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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