Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02286947 · ClinicalTrials.gov registry record · Phase 2

Safety Study of Eteplirsen to Treat Advanced Stage Duchenne Muscular Dystrophy

A Phase 2 study, sponsored by Sarepta Therapeutics.

Completed
Registry status
Phase 2
Development phase
24
Enrollment target

NCT02286947: Completed Phase 2 study, sponsored by Sarepta Therapeutics.

NCT02286947 is a Phase 2 study that has completed, run by Sarepta Therapeutics. The registered enrollment target is 24 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (82% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02286947, a Phase 2 study, has completed, sponsored by Sarepta Therapeutics.

COMPLETED
Registry status
Phase 2
Development phase
24 participants
Enrollment target

Study Summary

The primary objective of this study is to explore safety and tolerability of eteplirsen in participants with advanced stage Duchenne muscular dystrophy (DMD) who are amenable to exon 51 skipping.

Primary Outcome

An adverse event (AE) was any untoward medical occurrence in a participant that did not necessarily have a causal relationship with the study drug. A serious adverse event (SAE) was an AE resulting in any of the following outcomes: death; Life-threatening event; Required or prolonged inpatient hospitalization; persistent or significant disability/incapacity; congenital anomaly. Treatment-emergent AEs were events that developed or worsened during the on-treatment period (defined as time from firs

Interventions

  • DRUG Eteplirsen

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2014-11
Est. Completion 2018-03-23
Phase Phase 2
Sarepta Therapeutics

33 total trials

What the finished NCT02286947 record still lists

NCT02286947 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (82% lower).

The record links to 0 conditions, and to 1 intervention - of which Eteplirsen is the first listed.

NCT02286947 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02286947 about?

NCT02286947 is a clinical study titled "Safety Study of Eteplirsen to Treat Advanced Stage Duchenne Muscular Dystrophy". The primary objective of this study is to explore safety and tolerability of eteplirsen in participants with advanced stage Duchenne muscular dystrophy (DMD) who are amenable to exon 51 skipping.

What is the current status of trial NCT02286947?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 24 participants. The study started on 2014-11. Estimated completion is 2018-03-23.

What interventions are being tested in trial NCT02286947?

The interventions under investigation include: Eteplirsen (DRUG).

Who is sponsoring clinical trial NCT02286947?

This trial is sponsored by Sarepta Therapeutics, which has 33 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02286947's enrollment target sits among peer trials

24 1756th of 2000 higher than 217 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02331979 · 24 participants · NA

    Improving Bladder Function in SCI by Neuromodulation

  • NCT03096197 · 24 participants · NA

    Exoskeleton and Spinal Cord Stimulation for SCI

  • NCT03223922 · 24 participants · NA

    Neurocognitive Functioning With Genu-Sparing Whole Brain Radiation Therapy for Brain Metastases

  • NCT03326921 · 24 participants · Phase 1

    HA-1 T TCR T Cell Immunotherapy for the Treatment of Patients With Relapsed or Refractory Acute Leukemia After Donor Stem Cell Transplant

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02286947, the US trial registry maintained by the National Library of Medicine. NCT02286947 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.