Protease inhibitors (PIs) are a class of antiviral drugs that are widely used to treat HIV/AIDS and hepatitis C. Protease inhibitors prevent viral replication by selectively binding to viral proteases (e.g. HIV-1 protease) and blocking proteolytic cleavage of protein precursors that are necessary for the production of infectious viral particles.
Protease inhibitors that have been developed and are currently used in clinical practice include:
- Antiretroviral HIV-1 protease inhibitors — class stem –navir:23
- Hepatitis C virus NS3/4A protease inhibitors — class stem –previr:26
Given the specificity of the target of these drugs there is the risk, as in antibiotics, of the development of drug-resistant mutated viruses. To reduce this risk it is common to use several different drugs together that are each aimed at different targets.
Protease inhibitors were the second class of antiretroviral drugs developed. The first members of this class, saquinavir and ritonavir, were approved in late 1995–1996. Within 2 years, annual deaths from AIDS in the United States fell from over 50,000 to approximately 18,000 Prior to this the annual death rate had been increasing by approximately 20% each year.
|Name||Trade name||Company||Patent||FDA approval date||Notes|
|Saquinavir||Invirase, Fortovase||Hoffmann–La Roche||U.S. Patent 5,196,438||December 6, 1995||The first protease inhibitor approved by the U.S. Food and Drug Administration (FDA).|
|Ritonavir||Norvir||Abbott||U.S. Patent 5,541,206||March 1, 1996||—|
|Indinavir||Crixivan||Merck & Co.||U.S. Patent 5,413,999||March 13, 1996||—|
|Nelfinavir||Viracept||Hoffmann–La Roche||U.S. Patent 5,484,926||March 14, 1997||—|
|Amprenavir||Agenerase||GlaxoSmithKline||U.S. Patent 5,585,397||April 15, 1999||The sixteenth FDA-approved antiretroviral. It was the first protease inhibitor approved for twice-a-day dosing instead of needing to be taken every eight hours. The convenient dosing came at a price, as the dose required is 1,200 mg, delivered in 8 very large gel capsules. Production was discontinued by the manufacturer December 31, 2004, as it has been superseded by fosamprenavir.|
|Lopinavir||Kaletra||Abbott||U.S. Patent 5,914,332||September 15, 2000||Is only marketed as a fixed-dose combination with ritonavir (see lopinavir/ritonavir).|
|Atazanavir||Reyataz||Bristol-Myers Squibb||U.S. Patent 5,849,911||June 20, 2003||Atazanavir was the first PI approved for once-daily dosing. It appears to be less likely to cause lipodystrophy and elevated cholesterol as side effects. It may also not be cross-resistant with other PIs.|
|Fosamprenavir||Lexiva, Telzir||GlaxoSmithKline||—||October 20, 2003||A prodrug of amprenavir. The human body metabolizes fosamprenavir in order to form amprenavir, which is the active ingredient. That metabolization increases the duration that amprenavir is available, making fosamprenavir a slow release version of amprenavir and thus reduces the number of pills required versus standard amprenavir.|
|Tipranavir||Aptivus||Boehringer Ingelheim||—||June 22, 2005||Also known as tipranavir disodium.|
|Darunavir||Prezista||Janssen Therapeutics||U.S. Patent 6,248,775||June 23, 2006||As of 2016, darunavir is an OARAC recommended treatment option for treatment-naïve and treatment-experienced adults and adolescents. Several ongoing phase III trials are showing a high efficiency for the darunavir/ritonavir combination being superior to the lopinavir/ritonavir combination for first-line therapy. Darunavir is the first drug in a long time that didn't come with a price increase. It leapfrogged two other approved drugs of its type, and is matching the price of a third.|
Researchers are investigating the use of protease inhibitors developed for HIV treatment as anti-protozoals for use against malaria and gastrointestinal protozoal infections:
- A combination of ritonavir and lopinavir was found to have some effectiveness against Giardia infection.
- The drugs saquinavir, ritonavir, and lopinavir have been found to have anti-malarial properties.
- A cysteine protease inhibitor drug was found to cure Chagas disease in mice.
Researchers are investigating whether protease inhibitors could possibly be used to treat cancer. For example, nelfinavir and atazanavir are able to kill tumor cells in culture (in a Petri dish). This effect has not yet been examined in humans; but studies in laboratory mice have shown that nelfinavir is able to suppress the growth of tumors in these animals, which represents a promising lead towards testing this drug in humans as well.
Protease inhibitors can cause a syndrome of lipodystrophy, hyperlipidemia, diabetes mellitus type 2, and kidney stones. This lipodystrophy is colloquially known as "Crix belly", after indinavir (Crixivan).
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