Novartis Receives FDA Approval for Rhapsido (remibrutinib) for Chronic Spontaneous Urticaria

Novartis (NYSE:NVS) is one of the best growth stocks to buy now. On September 30, Novartis announced the US FDA approval of its drug, Rhapsido (remibrutinib). This oral pill is approved for use in adult patients with chronic spontaneous urticaria/CSU whose symptoms persist despite treatment with H1 antihistamines.

Rhapsido is a pill taken twice daily and is significant because it is the first oral, targeted Bruton’s tyrosine kinase inhibitor/BTKi to be FDA-approved for CSU, offering a non-injectable option that does not require routine lab monitoring. Rhapsido targets the core mechanism of CSU, which is a mast cell-driven condition thought to be caused by immune dysregulation.

Novartis Receives FDA Approval for Rhapsido (remibrutinib) for Chronic Spontaneous Urticaria

The drug works by blocking the activity of the BTK protein in immune cells, which in turn helps to inhibit the release of histamine and other proinflammatory mediators. This is a crucial development for the 1.7 million people in the US living with CSU, as over half of them remain symptomatic even with increased doses of standard antihistamines, and fewer than 20% of eligible patients currently receive existing injectable treatments.

Novartis (NYSE:NVS) researches, develops, manufactures, distributes, markets, and sells pharmaceutical medicines in Switzerland and internationally.

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Disclosure: None. This article is originally published at Insider Monkey.