Ionis Pharmaceuticals. has filed a patent for administering ISIS 678354 to treat Familial Chylomicronemia Syndrome, Familial Partial Lipodystrophy, and Severe Hypertriglyceridemia by reducing APOCIII RNA or protein levels in human subjects. The method aims to alleviate symptoms such as abdominal pain, fatigue, and pancreatitis. GlobalData’s report on Ionis Pharmaceuticals gives a 360-degree view of the company including its patenting strategy. Buy the report here.
According to GlobalData’s company profile on Ionis Pharmaceuticals, Nucleic acid active pharmaceutical ingredient was a key innovation area identified from patents. Ionis Pharmaceuticals's grant share as of January 2024 was 38%. Grant share is based on the ratio of number of grants to total number of patents.
A patent application (Publication Number: US20240033280A1) discloses a method for treating Familial Chylomicronemia Syndrome (FCS) by reducing APOCIII RNA or protein levels in human subjects. The method involves administering a compound with a specific chemical structure subcutaneously or intrathecally every 4 weeks. The compound, represented by SEQ ID NO: 3, or its salt, is administered in doses of 50 mg or 80 mg to alleviate symptoms of FCS. Additionally, the compound can be a sodium or potassium salt, and a modified oligonucleotide with specific nucleobases, sugar moieties, and internucleoside linkages can also be used for treatment.
Furthermore, the method outlined in the patent application targets severe symptoms associated with FCS, such as elevated chylomicrons and triglyceride levels, abdominal pain, fatigue, cognitive difficulties, diarrhea, pancreatitis, xanthomata, and hepatosplenomegaly. The treatment regimen involves regular subcutaneous administration of the compound every 4 weeks to address these symptoms effectively. The compound's specific chemical structure and mode of administration aim to reduce APOCIII RNA or protein levels, providing relief to individuals suffering from FCS. The patent application emphasizes the importance of addressing these symptoms to improve the quality of life for patients with FCS.
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