Rupintrivir: Difference between revisions

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Latest revision as of 01:30, 20 February 2025

Rupintrivir is a protease inhibitor that was originally developed for the treatment of rhinovirus infections. It is a 3C protease inhibitor, which means it inhibits the 3C protease enzyme, a crucial component in the life cycle of picornaviruses. Rupintrivir was developed by Agouron Pharmaceuticals, a subsidiary of Pfizer.

History[edit]

Rupintrivir was first synthesized in the late 1990s by Agouron Pharmaceuticals. The drug was developed as a potential treatment for the common cold, which is most often caused by rhinovirus infections. However, despite showing promise in early-stage clinical trials, development of the drug was discontinued in the early 2000s due to a lack of efficacy in later-stage trials.

Mechanism of Action[edit]

Rupintrivir works by inhibiting the 3C protease enzyme, a key component in the life cycle of picornaviruses. By blocking this enzyme, the drug prevents the virus from replicating and spreading within the body.

Clinical Trials[edit]

In early-stage clinical trials, rupintrivir was shown to reduce the duration and severity of cold symptoms in patients infected with rhinovirus. However, in later-stage trials, the drug did not show a significant benefit over placebo, leading to the discontinuation of its development.

Future Research[edit]

Despite the discontinuation of rupintrivir's development, research into 3C protease inhibitors continues. These drugs have the potential to treat a wide range of viral infections, including those caused by enteroviruses and noroviruses.

See Also[edit]

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