Spinal Muscular Atrophy Babies may Now Stand a Chance With the New Drug

An experimental Drug - RG7916 shows promise in treating babies with spinal muscular atrophy, finds a new study. These patients can usually survive for up to 10.5 months otherwise.

RG7916, the new investigational drug can help increase the level of survival motor neuron (SMN) proteins, which are usually lacking in babies with spinal muscular atrophy. The findings of this study are going to be presented at American Academy of Neurology's 70th Annual Meeting.

Spinal muscular atrophy (SMA) is an inherited disease that leads to loss of motor function. It is the leading genetic cause of death in infants and toddlers. The disease is caused by reduced levels of the survival motor neuron (SMN) protein. In SMA, the SMN1 gene is mutated or missing. The backup SMN2 gene allows production of some of the necessary protein.

New Born Screening For Spinal Muscular Atrophy To Lower Disease Severity
Approximately 1 in 40 of the general population are genetic carriers of spinal muscular atrophy but there is no screening programme for SMA in UK.

‘Since the spinal muscular atrophy is the result of reduced levels of the survival motor neuron (SMN) protein. The new drug RG7916 can modulate the SMN2 gene splicing to increase SMN protein and thereby increase survival chances.’

The new drug, called RG7916, is a liquid solution given orally once a day. It is designed to modulate the SMN2 gene splicing to increase SMN protein.

The study involved babies with type 1 spinal muscular atrophy who have two copies of the SMN2 gene. On average, these babies survive for 10.5 months before they die or need permanent breathing support.

The first phase of the study involved 21 babies who were three to seven months old at the start of the study. They were given the drug every day for four weeks at different dose levels.

SMN Protein Acts Like a 'Matchmaker' in Spinal Muscular Atrophy
The puzzling question - 'Why does interfering with a process that happens everywhere affect motor neurons first?' - has lurked behind spinal muscular atrophy.

Study results showed an increase of the SMN protein in the blood, with greater increases for higher doses of the drug. For the highest dose, the levels were up to 6.5 times higher after four weeks of treatment compared to levels at the beginning of the study.

At the time of the analysis, 19 babies were alive. The two fatal events reported were disease-related and not considered related to the investigational drug. The average study duration for the 19 babies was four months with a range of one month to 13.5 months.

Advertisements

New Molecule May Help Treat Spinal Muscular Atrophy
Researchers at the University of Missouri developed a new molecule in April 2014 that was found to be highly effective in animal models exhibiting spinal muscular atrophy.

None of the 19 babies lost the ability to swallow, needed a tracheostomy for breathing or needed permanent breathing support during the study. There were no safety problems that required any babies to be removed from the study.

"These results are exciting, as children with SMA type 2, which is less severe than type 1, have approximately twice as much SMN protein as those with type 1 so to see an increase of up to 6.5 times the amount of protein is very encouraging and supports the possibility to see improved function in these babies," said study author Giovanni Baranello, MD, PhD, at the Carlo Besta Neurological Institute in Milan, Italy. "This research is continuing, and much more needs to be done to determine whether this treatment will provide meaningful benefits for children with spinal muscular atrophy."