Skip to main content
MedPathMedPath Home
Clinical Trials/CTIS2024-511707-42-00
CTIS2024-511707-42-00
Active, not recruiting
Phase 1

ong-term Follow-up of Patients with Spinal Muscular Atrophy Treated with OAV101 IT or OAV101 IV in Clinical Trials - COAV101A12308

ovartis Pharma AG0 sites160 target enrollmentJuly 10, 2024
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit
ConditionsSpinal Muscular AtrophyMedDRA version: 20.1Level: PTClassification code: 10041582Term: Spinal muscular atrophy Class: 100000004850Therapeutic area: Diseases [C] - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Spinal Muscular Atrophy
Sponsor
ovartis Pharma AG
Enrollment
160
Status
Active, not recruiting
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 10, 2024
End Date
TBD
Last Updated
last year
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Participated in an OAV101 clinical trial., Written informed consent must be obtained before any assessment is performed., 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

Not yet recruiting
Phase 3
ong-term Follow-up of Patients with Spinal Muscular Atrophy Treated with OAV101 in Clinical trials
JPRN-jRCT2033230642Hirano Takamitsu4
Active, not recruiting
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]
EUCTR2021-006781-21-BEovartis Pharma AG260
Active, not recruiting
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]
EUCTR2021-006781-21-FRovartis Pharma AG260
Active, not recruiting
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]
EUCTR2021-006781-21-DKovartis Pharma AG260
Not yet recruiting
Phase 3
ong-term follow-up of patients with spinal muscular atrophy Treated with OAV101 IT or OAV101 IV in Clinical Trialsspinal muscular atrophy1002830210029317
NL-OMON56701ovartis2