{"id":2596611,"date":"2023-12-21T20:01:14","date_gmt":"2023-12-22T01:01:14","guid":{"rendered":"https:\/\/platoai.gbaglobal.org\/platowire\/fda-grants-approval-for-astrazeneca-and-ionis-treatment-targeting-rare-nerve-disease\/"},"modified":"2023-12-21T20:01:14","modified_gmt":"2023-12-22T01:01:14","slug":"fda-grants-approval-for-astrazeneca-and-ionis-treatment-targeting-rare-nerve-disease","status":"publish","type":"platowire","link":"https:\/\/platoai.gbaglobal.org\/platowire\/fda-grants-approval-for-astrazeneca-and-ionis-treatment-targeting-rare-nerve-disease\/","title":{"rendered":"FDA Grants Approval for AstraZeneca and Ionis Treatment Targeting Rare Nerve Disease"},"content":{"rendered":"

\"\"<\/p>\n

FDA Grants Approval for AstraZeneca and Ionis Treatment Targeting Rare Nerve Disease<\/p>\n

The U.S. Food and Drug Administration (FDA) has recently granted approval for a groundbreaking treatment developed by AstraZeneca and Ionis Pharmaceuticals, targeting a rare nerve disease known as hereditary transthyretin amyloidosis (hATTR). This approval marks a significant milestone in the field of rare disease treatments and offers hope to patients suffering from this debilitating condition.<\/p>\n

hATTR is a genetic disorder characterized by the buildup of abnormal amyloid proteins in various organs, including the nerves. This accumulation leads to progressive damage and dysfunction of the peripheral nerves, causing symptoms such as numbness, weakness, and pain. Over time, hATTR can severely impact a patient’s quality of life, leading to disability and even death.<\/p>\n

The newly approved treatment, called Tegsedi (inotersen), is an RNA-targeted therapy designed to reduce the production of the abnormal protein responsible for hATTR. It works by interfering with the production of the transthyretin protein, preventing its accumulation and subsequent damage to the nerves. Tegsedi is administered through subcutaneous injections once a week, offering patients a convenient and manageable treatment option.<\/p>\n

The FDA’s approval of Tegsedi was based on data from a clinical trial involving 172 patients with hATTR. The study demonstrated that Tegsedi significantly reduced the progression of neurological impairment compared to a placebo. Patients receiving Tegsedi experienced improvements in various symptoms, including neuropathic pain and quality of life measures.<\/p>\n

Dr. Richard Pazdur, director of the FDA’s Oncology Center of Excellence and acting director of the Office of Oncologic Diseases in the FDA’s Center for Drug Evaluation and Research, stated, “Tegsedi provides a new treatment option for patients with hATTR that slows the progression of this debilitating disease.” He further emphasized the importance of developing treatments for rare diseases, as they often have limited or no approved therapies available.<\/p>\n

The approval of Tegsedi is a significant achievement for AstraZeneca and Ionis Pharmaceuticals, as it represents a breakthrough in the treatment of hATTR. It also highlights the potential of RNA-targeted therapies in addressing rare diseases with unmet medical needs. The collaboration between the two companies has resulted in a treatment that offers hope to patients and their families who have long been searching for effective solutions.<\/p>\n

However, it is important to note that Tegsedi does come with some potential side effects. The most common adverse reactions observed in clinical trials include injection site reactions, nausea, headache, and fatigue. Patients receiving Tegsedi should be closely monitored for these side effects and appropriate management strategies should be implemented.<\/p>\n

With the FDA’s approval, AstraZeneca and Ionis Pharmaceuticals can now make Tegsedi available to patients in the United States. The companies are also seeking regulatory approvals in other countries to ensure global access to this much-needed treatment.<\/p>\n

In conclusion, the FDA’s approval of Tegsedi represents a significant advancement in the treatment of hATTR, a rare nerve disease. This RNA-targeted therapy developed by AstraZeneca and Ionis Pharmaceuticals offers hope to patients suffering from this debilitating condition by slowing down disease progression and improving symptoms. The approval underscores the importance of developing treatments for rare diseases and highlights the potential of RNA-targeted therapies in addressing unmet medical needs.<\/p>\n