Clinical trial news

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,…

According to a report on postbulletin.com, there are 33 states that have right-to-try laws, giving people with life-threatening illnesses access to drugs that have not yet been approved by the FDA. MORE: West Virginia boy hopes to get Spinraza treatment for SMA. So long as the drug has safely completed the…

Cytokinetics has begun enrolling a second group of patients for a Phase 2 clinical trial of CK-2127107 as a treatment for spinal muscular atrophy (SMA). The announcement follows an independent Data Monitoring Committee’s review of the therapy’s safety, absorption, distribution, metabolism, and excretion in Cohort 1. The randomized, double-blind, placebo-controlled,…

According to the Daily Mail, Lexi Pacini from Colorado has made incredible progress while using Spinraza. Lexi’s parents felt something was amiss with their little girl when she failed to meet the same development milestones her older sister had. At 11 months old, Lexi still hadn’t learned to crawl so they took her to…