Clinical trial news

Cure SMA has released a booklet highlighting the importance of clinical trials for research into better treatments and therapies for spinal muscular atrophy (SMA) patients. MORE: Phase 2 clinical trial of oral compound targeting genetic cause of SMA starts in Europe. The brochure explains the processes involved…

Spinraza webinar Discussion

The patient advocacy group Cure SMA will host a webinar May 4 on access to Spinraza (nusinursen), the first drug ever to be approved to treat spinal muscular atrophy (SMA). The webinar will cover several topics, including the current status of Spinraza dosing at U.S. administration sites, commercial and government insurance policies, trial…

Spinraza and SMA Discussion

A Phase 3 clinical trial evaluating Spinraza (nusinersen) in children with type 2 spinal muscular atrophy (SMA) may play a decisive role in whether private insurers cover the treatment in later-onset SMA patients — those with type 2 and type 3. The study was the focus of an Emerging Science…

A gene therapy may be able to help babies with type 1 spinal muscular atrophy (SMA). AveXis has published the results of the first phase of a clinical trial for its drug AVXS-101 which aims to deliver a working copy of the SMN gene to the patient’s motor neuron cells,…