Clinical trial news

In this heartwarming video from Robert Harding, we meet Cameron. Cameron was diagnosed with type 1 spinal muscular atrophy (SMA) at five weeks old and was given just six to 12 months to live. The family decided to enroll Cameron in a clinical trial for the drug nusinersen and…

Spinraza for later-onset SMA

Spinraza (nusinersen) for spinal muscular atrophy (SMA) met the primary endpoint in an interim analysis from a Phase 3 clinical trial evaluating the treatment in children with later-onset (consistent with Type 2) SMA. Biogen and Ionis Pharmaceuticals reported that children treated with Spinraza had a highly statistically significant improvement in motor…

SMA treatment development

AveXis reported that the planned pivotal clinical trial of its gene therapy candidate AVXS-101 for spinal muscular atrophy (SMA) Type 1 will enroll about 20 patients and will have a single-arm design, with the comparator being the natural disease history. This update follows the Type B meeting Sept. 30 with the…

Phase 2 SMA studies

A spinal muscular atrophy (SMA) collaboration has two Phase 2 clinical trials aligned to evaluate the safety, tolerability, and effectiveness of the investigational drug RG7916 in pediatric and adult patients of Type 2 and Type 3 SMA and in pediatric patients of Type 1 SMA. The SMA development program…

pneumonia

In a late-breaking session at the 2016 World Muscle Society Congress in Granada, Spain, Biogen and Ionis Pharmaceuticals presented new data from clinical trials for their co-developed drug candidate nusinersen for treating spinal muscular atrophy (SMA). Nusinersen, a potentially disease-modifying SMA therapy, is an antisense oligonucleotide (ASO) designed to…