A rare genetic condition, Spinal Muscular Atrophy (SMA) affects one in 7,000 people in India. It mostly affects children and ...
A Prescription Drug User Fee Act (PDUFA) target action date for apitegromab has been set for Sept. 22, 2025.
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LancsLive on MSN'We waited months for answers over our baby's condition - now he'll never be able to walk'“During the wait for the results, things deteriorated. He was choking constantly, not going to the toilet for days and his ...
Chugai Pharma’s Evrysdi tablets 5mg receives Japanese approval to treat spinal muscular atrophy: Saturday, March 29, 2025, 11:00 Hrs [IST] Chugai Pharmaceutical Co., Ltd. announ ...
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Independent.ie on MSN‘Every day counts’ – call to add screening for rare muscle-wasting condition to newborns’ ‘heel-prick’ testA majority of people have supported the urgent implementation of early screening for a genetic disease that causes severe ...
Here is our list of the 11 Best Gene Therapy Stocks to Buy According to Analysts.
“We were referred to a paediatrician who put him on reflux medication. However, things were getting worse,” Ellie said. “He ...
"Roche has filed an appeal against the Hon. Delhi High Court order and the matter is subjudice in the appeal court," Roche ...
Speakers from the Muscular Dystrophy Association (MDA) highlighted 75 years of progress in understanding and treating ...
Roche had appealed against a single judge order of March 24 that had refused to stop Natco Pharma from manufacturing a generic version of Risdiplam ...
Biogen enhances its portfolio and margins amidst market challenges and competition. Click here to find out why BIIB stock is ...
In a major relief to Indian drugmaker Natco Pharma, the Delhi High Court has rejected an interim injunction plea filed by ...
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