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Clinical Trials/NL-OMON56701
NL-OMON56701
Not yet recruiting
Phase 3

ong-term follow-up of patients with spinal muscular atrophy Treated with OAV101 IT or OAV101 IV in Clinical Trials - OAV101

ovartis0 sites2 target enrollmentTBD
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Conditionsspinal muscular atrophy1002830210029317

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
spinal muscular atrophy
Sponsor
ovartis
Enrollment
2
Status
Not yet recruiting
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Observational invasive

Investigators

Sponsor
ovartis

Eligibility Criteria

Inclusion Criteria

  • •Participants eligible for inclusion in this study must meet all of the
  • •following criteria:
  • •1\. Participated in an OAV101 clinical trial.
  • •2\. Written informed consent must be obtained before any assessment is performed.
  • •3\. Patient/Parent/legal guardian willing and able to comply with study
  • •procedures.

Exclusion Criteria

  • •There are no specific exclusion criteria for this study.

Outcomes

Primary Outcomes

Not specified

Similar Trials

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Phase 1
ong-term follow-up of patients with spinal muscular atrophy Treated with OAV101 in Clinical TrialsSpinal Muscular AtrophyMedDRA version: 20.1Level: PTClassification code 10041582Term: Spinal muscular atrophySystem Organ Class: 10010331 - Congenital, familial and genetic disordersTherapeutic area: Diseases [C] - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
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ong-term follow-up of patients with spinal muscular atrophy Treated with OAV101 in Clinical TrialsSpinal Muscular AtrophyMedDRA version: 20.1Level: PTClassification code 10041582Term: Spinal muscular atrophySystem Organ Class: 10010331 - Congenital, familial and genetic disordersTherapeutic area: Diseases [C] - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
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ong-term follow-up of patients with spinal muscular atrophy Treated with OAV101 in Clinical TrialsSpinal Muscular AtrophyMedDRA version: 20.1Level: PTClassification code 10041582Term: Spinal muscular atrophySystem Organ Class: 10010331 - Congenital, familial and genetic disordersTherapeutic area: Diseases [C] - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
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ong-term Follow-up of Patients with Spinal Muscular Atrophy Treated with OAV101 in Clinical trials
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