Zolgensma shows impressive results in older children when administered by intrathecal injection

A gene therapy approved for treating spinal muscular atrophy in infants has also shown improved efficacy in older children.

Basel, Switzerland-based drugmaker Novartis said Saturday that interim data from a Phase I/II study of Zolgensma showed an increase by several points on a scale used to evaluate motor function in children aged 2 to less than 5 with untreated SMA Type 2 when administered into an area of the spine. Patients achieved a median increase of 5.9 points from baseline on the Hammersmith functional motor scale-expanded, or HFMSE, compared with a median increase of 4.2 points when data were presented in May at the American Academy of Neurology’s annual meeting.

Please click here to read the full company press release.

Latest Posts

  • Calling on all the community to ACT NOW to avoid losing treatments!

    Calling on all the community to ACT NOW to avoid losing treatments!

    Currently, there are two approved treatments for SMA: risdiplam and nusinersen. These treatments were initially approved temporarily under Managed Access Agreements while the NHS and NICE gathered data to assess their cost-effectiveness. Now, as these agreements come to an end, both treatments face a crucial review.

    Read more

  • NICE’s upcoming Multi Technology Assessment for Spinraza and Risdiplam

    NICE’s upcoming Multi Technology Assessment for Spinraza and Risdiplam

    SMA UK are proud to join together with Treat SMA and MDUK to bring you this webinar about NICE’s upcoming Multi Technology Assessment for Spinraza and Risdiplam. 2024 sees the end of the managed access agreements (MAAs) for the two treatments. An expert committee will gather to assess the new clinical and real-world evidence, along…

    Read more

  • Let the battle begin

    Let the battle begin

    This year the Managed Access Agreement for Spinraza and Risdiplam expires. The MAA was put in place five years ago so the pharmaceutical companies could gather more evidence to resubmit to NICE for approval on the NHS with Biogen extending their MAA by a year.

    Read more