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While the findings suggest that switching to onasemnogene abeparvovec after non–gene therapy treatments could be beneficial to patients with spinal muscular atrophy, it is not clear which patients may benefit the most from switching therapies. | Image credit: Rochu_2008 - stock.adobe.com
Switching to Gene Therapy After Nusinersen or Risdiplam May Benefit Patients With SMA

August 15th 2025

Children with spinal muscular atrophy (SMA) showed motor function improvements after switching to onasemnogene abeparvovec following prior treatment with nusinersen or risdiplam in a real-world study.

The long-term data from DELIVER showed meaningful, sustained improvements in functional outcomes and dystrophin expression, as well as a favorable safety profile in patients with Duchenne muscular dystrophy. | Image credit: OlegKachura - stock.adobe.com
DYNE-251 Granted FDA Breakthrough Therapy Designation for DMD

August 13th 2025

AJMC
The Impact of Health Benefit Design on Patients With Infertility

August 5th 2025

ROS1-positive NSCLC is aggressive and rare, with approximately 3000 new diagnoses of advanced disease in the US each year. | Image credit: appledesign - stock.adobe.com
Taletrectinib Recommended in NCCN Guidelines for ROS1-Positive NSCLC

July 31st 2025

PA form | Image: Adobe Stock
KFF Survey: Most Consumers Find Prior Authorization Is a Major Problem

July 25th 2025

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