Taribavirin

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Taribavirin
Taribavirin 3D ball

Taribavirin, also known by its international nonproprietary name (rINN) as viramidine and codenamed ICN 3142, is an antiviral drug candidate that has progressed to Phase III clinical trials, but is yet to receive approval for medical use. Structurally, it is a prodrug of ribavirin and exhibits antiviral activity against a spectrum of DNA and RNA viruses. The potential advantages and clinical implications of Taribavirin over its counterpart, ribavirin, have caught the attention of researchers and clinicians alike.

Historical Context[edit | edit source]

Taribavirin was first introduced to the scientific community in 1973 by J.T. Witkowski et al. during their tenure at ICN Pharmaceuticals. Their primary objective was to identify a derivative of ribavirin that would exhibit superior antiviral properties. In contemporary research and development, Valeant Pharmaceuticals International has taken the reins in advancing Taribavirin, especially as a potential remedy for chronic hepatitis C.

Mechanism and Pharmacological Features[edit | edit source]

Taribavirin's antiviral capabilities emanate from its status as a prodrug of ribavirin. It demonstrates potency against several DNA and RNA viruses, positioning it as a prospective candidate for various viral infections.

Targeting and Metabolism[edit | edit source]

Distinctively, Taribavirin showcases enhanced liver-targeting compared to ribavirin. Moreover, its shorter systemic duration can be attributed to its reduced penetration and accumulation within red blood cells. Upon reaching the liver, Taribavirin undergoes metabolic transformation, resulting in higher concentrations of ribavirin in liver cells and bile.

Pharmacological Nuances[edit | edit source]

It's noteworthy that the carboxamidine group in Taribavirin exhibits a basic characteristic. Hence, the drug is often recognized and administered as the hydrochloride salt variant, with a corresponding ".HCl" chemical formula. At physiological pH levels, the partial protonation of the carboximide group lends a positive charge to the molecule, slowing its passage through cell membranes until metabolized into ribavirin.

Clinical Implications and Potential Uses[edit | edit source]

The promise of Taribavirin lies in its potential to serve as an alternative to ribavirin in treating specific viral hepatitis syndromes, notably hepatitis C. Additionally, there are possibilities of its application against hepatitis B and yellow fever.

Furthermore, in animal models, Taribavirin has demonstrated comparable activity to ribavirin against influenza, but with marginally reduced toxicity. This raises the potential of Taribavirin eventually substituting ribavirin as an anti-influenza agent.

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Contributors: Prab R. Tumpati, MD