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Clinical Trials/NL-OMON51427
NL-OMON51427Not yet recruitingPhase 2

Escalating Dose and Randomized, Controlled Study of Nusinersen (BIIB058) in Participants With Spinal Muscular Atrophy - 232SM203 (Devote)

Biogen Idec Research Limited0 sites4 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Phase 2
Status
Not yet recruiting
Enrollment
4

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
0 to 1 (—)

Inclusion Criteria

  • - Genetic documentation of 5q SMA (homozygous gene deletion, mutation, or
  • compound heterozygote)
  • - Participants with SMA symptom onset <= 6 months (<= 180 days) of age (infantile
  • onset) should have age > 1 week to <= 7 months (<= 210 days) at the time of
  • informed consent
  • - Participants with SMA symptom onset > 6 months (> 180 days) of age (later
  • - Age 2 to < 10 years at the time of informed consent
  • - Can sit independently but has never had the ability to walk independently
  • - HFMSE score >= 10 and <= 54 at Screening

Exclusion Criteria

  • - Presence of an untreated or inadequately treated active infection requiring
  • systemic antiviral or antimicrobial therapy at any time during the Screening
  • - Presence of an implanted shunt for the drainage of CSF or of an implanted
  • central nervous system (CNS) catheter
  • - Hospitalization for surgery, pulmonary event, or nutritional support within 2
  • months prior to Screening or planned within 12 months after the participant's
  • - Treatment with an investigational drug including but not limited to the
  • treatment of SMA, biological agent, or device within 30 days or 5 half-lives of
  • the agent, whichever is longer, prior to Screening or anytime during the study;
  • any prior or current treatment with any survival motor neuron-2 (SMN2)-
  • splicing modifier or gene therapy; or prior antisense oligonucleotide
  • treatment, or cell transplantation
  • - Participants with SMA symptom onset > 6 months (> 180 days) of age (later
  • - Respiratory insufficiency, defined by the medical necessity for invasive or
  • noninvasive ventilation for > 6 hours during a 24-hour period, at Screening
  • - Medical necessity for a gastric feeding tube
  • - Participants with SMA symptom onset <= 6 months (<= 180 days) of age (infantile
  • onset): Signs or symptoms of SMA present at birth or within the first week
  • after birth

Investigators

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