Trial intelligence / Profile preview

Long-term Open-label Extension Study of Casimersen or Golodirsen in Duchenne Muscular Dystrophy

2017-004625-32Phase 3Completed

Sponsor
Sarepta Therapeutics
Start
Jul 2018
Modality
Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, MicroRNA (miRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense Oligonucleotides (ASOs) → Long RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics
Countries
1
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Overview

Phase 3, open-label trial of casimersen and golodirsen in Duchenne muscular dystrophy (DMD) (2 arms), sponsored by Sarepta Therapeutics. Primary endpoint: Patient incidence of serious adverse events (SAEs). Started Jul 2018; status: completed.

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Drugs

casimersengolodirsen
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Conditions

Duchenne muscular dystrophy (DMD)

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