Registry of Patients With a Diagnosis of Spinal Muscular Atrophy (SMA)

Study Identifier:
COAV101A12001
ClinicalTrials.gov Identifier:
EudraCT Identifier:
N/A
EU CT Number:
N/A
Sponsor:
Novartis Pharmaceuticals
Recruiting

Study Details

Medical Condition
  • All Spinal Muscular Atrophies
Study Drug
  • Drug: Zolgensma
Date
Sep 2018 - Jun 2038
Patient Requirements
Sex: Female & Male
Age: N/A
Requirements Information

Protocol Summary

Spinal muscular atrophy (SMA) is a neurogenetic disorder caused by a loss or mutation in the survival motor neuron 1 gene (SMN1) on chromosome 5q13, which leads to reduced SMN protein levels and a selective dysfunction of motor neurons. SMA is an autosomal recessive, early childhood disease with an incidence of 1:10,000 live births. SMA is the leading cause of infant mortality due to genetic diseases.

The purpose of this registry is to assess the long term outcomes of patients with SMA in the context of advances in treatment options and also to characterize and assess long-term safety and effectiveness of OAV-101.

Trial Locations

Location
Status
Location
Phoenix Children's Hospital
Phoenix, Arizona, United States, 85016
Status
Recruiting
Location
Arkansas Children's Hospital
Little Rock, Arkansas, United States, 72202
Status
Recruiting
Location
Loma Linda University Health
Loma Linda, California, United States, 92350
Status
Completed
Location
Children's Hospital of Los Angeles
Los Angeles, California, United States, 90027
Status
Recruiting
Location
University of California Los Angeles Health
Los Angeles, California, United States, 90095
Status
Recruiting
Location
Valley Children's Healthcare
Madera, California, United States, 93636
Status
Recruiting
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