Background: Real-world data on the efficacy and safety of onasemnogene abeparvovec (OA) in spinal muscular atrophy (SMA) are needed, especially to overcome uncertainties around its use in older and heavier children. This study evaluated the efficacy and safety of OA in patients with SMA type 1 in the UK, including patients ≥2 years old and weighing ≥13.5 kg. / Methods: This observational cohort study used data from patients with genetically confirmed SMA type 1 treated with OA between May 2021 and January 2023, at 6 infusion centres in the United Kingdom. Functional outcomes were assessed using age-appropriate functional scales. Safety analyses included review of liver function, platelet count, cardiac assessments, and steroid requirements....
In a previous Phase 2 study, olesoxime had a favorable safety profile. Although the primary endpoint...
INTRODUCTION: This is the first description of safety data for intravenous onasemnogene abeparvovec,...
Background: Spinal muscular atrophy (SMA) is a progressive motor neuron disease causing loss of moto...
First published: 16 February 2022Objective: To provide a greater understanding of the tolerability, ...
BACKGROUND: Long-term, real-world effectiveness and safety data of disease-modifying treatments for ...
INTRODUCTION: This is the first description of safety data for intravenous onasemnogene abeparvovec,...
Background: Spinal muscular atrophy is a rare, autosomal recessive, neuromuscular disease caused by ...
peer reviewedBACKGROUND: Spinal muscular atrophy is a rare, autosomal recessive, neuromuscular disea...
Background Spinal muscular atrophy is a rare, autosomal recessive, neuromuscular disease caused by b...
BACKGROUND: Spinal muscular atrophy (SMA) is a devastating rare disease that affects individuals reg...
Objective To report cross-sectional clinical findings in a large cohort of patients affected by typ...
SPR1NT ( NCT03505099 ) was a Phase III, multicenter, single-arm study to investigate the efficacy an...
Spinal muscular atrophy is treated with onasemnogene abeparvovec, which replaces the missing surviva...
peer reviewedSPR1NT ( NCT03505099 ) was a Phase III, multicenter, single-arm study to investigate th...
BACKGROUND: Spinal muscular atrophy (SMA) is caused by a homozygous deletion of the survival motor n...
In a previous Phase 2 study, olesoxime had a favorable safety profile. Although the primary endpoint...
INTRODUCTION: This is the first description of safety data for intravenous onasemnogene abeparvovec,...
Background: Spinal muscular atrophy (SMA) is a progressive motor neuron disease causing loss of moto...
First published: 16 February 2022Objective: To provide a greater understanding of the tolerability, ...
BACKGROUND: Long-term, real-world effectiveness and safety data of disease-modifying treatments for ...
INTRODUCTION: This is the first description of safety data for intravenous onasemnogene abeparvovec,...
Background: Spinal muscular atrophy is a rare, autosomal recessive, neuromuscular disease caused by ...
peer reviewedBACKGROUND: Spinal muscular atrophy is a rare, autosomal recessive, neuromuscular disea...
Background Spinal muscular atrophy is a rare, autosomal recessive, neuromuscular disease caused by b...
BACKGROUND: Spinal muscular atrophy (SMA) is a devastating rare disease that affects individuals reg...
Objective To report cross-sectional clinical findings in a large cohort of patients affected by typ...
SPR1NT ( NCT03505099 ) was a Phase III, multicenter, single-arm study to investigate the efficacy an...
Spinal muscular atrophy is treated with onasemnogene abeparvovec, which replaces the missing surviva...
peer reviewedSPR1NT ( NCT03505099 ) was a Phase III, multicenter, single-arm study to investigate th...
BACKGROUND: Spinal muscular atrophy (SMA) is caused by a homozygous deletion of the survival motor n...
In a previous Phase 2 study, olesoxime had a favorable safety profile. Although the primary endpoint...
INTRODUCTION: This is the first description of safety data for intravenous onasemnogene abeparvovec,...
Background: Spinal muscular atrophy (SMA) is a progressive motor neuron disease causing loss of moto...