The label expansion means risdiplam is approved for spinal muscular atrophy for all ages.
The FDA this week approved an expanded indication for risdiplam (Evrysdi) to include the treatment of presymptomatic infants under 2 months old with spinal muscular atrophy (SMA).
It is the first approved treatment administered at home for this group.
The approval was based off interim efficacy and safety data from the RAINBOWFISH study, which showed that, following 12 months of treatment with risdiplam, most presymptomatic infants met key milestones of healthy babies. This included sitting, standing, and walking, in addition to maintaining the ability to swallow.
Risdiplam, a survival motor neuron splicing modifier, also had supportive data from the open-label extension FIREFISH study in its application. In a cohort of 58 infants aged 1 to 7 months, 91% were alive after 3 years of treatment with risdiplam. Among the 48 infants who had an available motor assessment, 32 infants maintained and 4 gained the ability to sit without support for at least 5 seconds since month 24, as assessed by the Gross Motor Scale of the Bayley Scores of Infant and Toddler Development.
Among the several ongoing trials of risdiplam, FIREFISH is unique in its 2-part design. Part 1 was a dose-escalation study in 21 infants with the primary end point assessing safety and determining the dosing for Part 2. In the single-arm Part 2, 41 infants with type 1 SMA were treated for 2 years, followed by an open-label extension. Original 2-year data from Part 2 were published in April 2021, with expanded results released in August 2021.
The most recent analysis of FIREFISH, announced earlier this month, pooled participants treated with the agent for a minimum of 3 years. At the conclusion of the analysis, 20 infants maintained and 15 gained the ability to sit without support for at least 30 seconds. No infant who gained the ability to sit without support lost this ability after 3 years, and the majority of infants also maintained the ability to feed orally and swallow up to that time point
Most infants showed the ability to improve or maintain measures on the Hammersmith Infant Neurological Examination between 24 and 36 months. This included being able to hold their heads upright (36 maintained, 3 gained, and none lost the ability since month 24), pivot while sitting (15 maintained, 11 gained, and none lost the ability), stand with support (6 maintained, 5 gained, and 1 lost the ability), and walk while holding on (1 maintained, 2 gained, and none lost the ability).
"The priority review and subsequent approval of Evrysdi for babies under 2 months of age speaks to the urgent ongoing need for additional treatment options for babies with SMA,” Levi Garroway, MD, PhD, chief medical officer, and head, Global Product Development, Genentech, said in a statement. “Because of its efficacy in multiple settings, Evrysdi is now available for people with SMA from presymptomatic newborns to older adults. We are proud of this achievement, which has the potential to make a real difference to those living with SMA and their caregivers."
Lack of Mutations Associated With Favorable Prognosis in MPN-U
April 25th 2024While the Dynamic International Prognostic Scoring System and bone marrow blasts may predict overall survival, the lack of certain mutations is also associated with a better prognosis for myeloproliferative neoplasm, unclassifiable (MPN-U).
Read More
HOPE-CAT Can Identify Maternal Cardiovascular Risk 2 Months Earlier Than Doctors, Study Says
April 25th 2024In a retrospective study, the machine learning tool was able to screen for potential risks of cardiovascular disease nearly 60 days before the patient's medical record showed any signs of a related condition or before they were officially diagnosed or treated for it.
Read More
Data Back Neoadjuvant Combo vs Chemo Alone for Early-Stage NSCLC
April 24th 2024For patients with early-stage non–small cell lung cancer (NSCLC), combining neoadjuvant immune checkpoint inhibitors and platinum-based chemotherapy improves 2-year outcomes over chemotherapy alone, suggest findings of an extensive literature review and meta-analysis.
Read More