Saquinavir

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Saquinavir
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Clinical data
Trade namesInvirase, Fortovase
Other namesSQV
AHFS/Drugs.comMonograph
MedlinePlusa696001
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Pregnancy
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Routes of
administration		By mouth
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Legal status
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Pharmacokinetic data
Bioavailability~4% (without ritonavir boosting)[3]
Protein binding98%
MetabolismLiver, mainly by CYP3A4
Elimination half-life9–15 hours
Excretionfeces (81%) and urine (3%)
Identifiers
  • (2S)-N-[(2S,3R)-4-[(3S)-3-(tert-butylcarbamoyl)-decahydroisoquinolin-2-yl]-3-hydroxy-1-phenylbutan-2-yl]-2-(quinolin-2-ylformamido)butanediamide
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Chemical and physical data
FormulaC38H50N6O5
Molar mass670.855 g·mol−1
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  • O=C(N)C[C@H](NC(=O)c1nc2c(cc1)cccc2)C(=O)N[C@@H](Cc3ccccc3)[C@H](O)CN5[C@H](C(=O)NC(C)(C)C)C[C@@H]4CCCC[C@@H]4C5
  • InChI=1S/C38H50N6O5/c1-38(2,3)43-37(49)32-20-26-14-7-8-15-27(26)22-44(32)23-33(45)30(19-24-11-5-4-6-12-24)41-36(48)31(21-34(39)46)42-35(47)29-18-17-25-13-9-10-16-28(25)40-29/h4-6,9-13,16-18,26-27,30-33,45H,7-8,14-15,19-23H2,1-3H3,(H2,39,46)(H,41,48)(H,42,47)(H,43,49)/t26-,27+,30-,31-,32-,33+/m0/s1 checkY
  • Key:QWAXKHKRTORLEM-UGJKXSETSA-N checkY
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Saquinavir, sold under the brand name Invirase among others, is an antiretroviral medication used together with other medications to treat or prevent HIV/AIDS.[4] Typically it is used with ritonavir or lopinavir/ritonavir to increase its effect.[4] It is taken by mouth.[4]

Common side effects include nausea, vomiting, diarrhea, and feeling tired.[4] More serious side effects include problems with QT prolongation, heart block, high blood lipids, and liver problems.[4] It appears to be safe in pregnancy.[4] It is in the protease inhibitor class and works by blocking the HIV protease.[4]

Saquinavir was patented in 1988 and first sold in 1995.[5][6]

Medical uses

Saquinavir is used together with other medications to treat or prevent HIV/AIDS.[4] Typically it is used with ritonavir or lopinavir/ritonavir to increase its effect.[4]

Side effects

The most frequent adverse events with saquinavir in either formulation are mild gastrointestinal symptoms, including diarrhoea, nausea, loose stools and abdominal discomfort. Invirase is better tolerated than Fortovase.[medical citation needed]

Bioavailability and drug interactions

Saquinavir, in the Invirase formulation, has a low and variable oral bioavailability, when given alone. The Fortovase formulation at the standard dosage delivers approximately eightfold more active drug than Invirase, also at the standard dosage.[7]

In the clinic, it was found that the oral bioavailability of saquinavir in both formulations significantly increases when patients also receive the PI ritonavir. For patients, this has the major benefit that they can take less saquinavir, while maintaining sufficient saquinavir blood plasma levels to efficiently suppress the replication of HIV.[medical citation needed]

The mechanism behind this welcome observation was not directly known, but later it was determined that ritonavir inhibits the cytochrome P450 3A4 isozyme. Normally, this enzyme metabolizes saquinavir to an inactive form, but with the ritonavir inhibiting this enzyme, the saquinavir blood plasma levels increased considerably. Additionally, ritonavir also inhibits multidrug transporters, although to a much lower extent.[medical citation needed]

Unlike other protease inhibitors, the absorption of saquinavir seems to be improved by omeprazole.[8]

Mechanism of action

Saquinavir is a protease inhibitor. Proteases are enzymes that cleave protein molecules into smaller fragments. HIV protease is vital for both viral replication within the cell and release of mature viral particles from an infected cell. Saquinavir binds to the active site of the viral protease and prevents cleavage of viral polyproteins, preventing maturation of the virus. Saquinavir inhibits both HIV-1 and HIV-2 proteases.[9]

History

File:HIV new infections and deaths 1981-2008.jpg
New HIV infections and deaths, before and after the FDA approval of "highly active antiretroviral therapy",[10] of which saquinavir, ritonavir and indinavir were key as the first three protease inhibitors.Page Module:Citation/CS1/styles.css has no content.Cully M (28 November 2018). "Protease inhibitors give wings to combination therapy". Nature Research. Open Publishing. Retrieved 28 October 2020. As a result of the new therapies, HIV deaths in the United States fell dramatically within two years.[10]

Saquinavir was developed by the pharmaceutical company Roche.[11] Saquinavir was the sixth antiretroviral and the first protease inhibitor approved by the US Food and Drug Administration (FDA), leading ritonavir and indinavir by a few months.[12] This new class of antiretrovirals played a critical role in the development of highly active antiretroviral therapy (HAART), which helped significantly lower the risk of death from AIDS-related causes, as seen by a reduction of the annual U.S. HIV-associated death rate, from over 50,000 to about 18,000 over a period of two years.[10][13]

Roche requested and received approval of Invirase via the FDA's "Accelerated Approval" program—a process designed to speed drugs to market for the treatment of serious diseases—a decision that was controversial, as AIDS activists disagreed over the benefits of thorough testing versus early access to new drugs.[14][better source needed] It was approved again on November 7, 1997, as Fortovase,[15] a soft gel capsule reformulated for improved bioavailability. Roche announced in May 2005 that, given reduced demand, Fortovase would cease being marketed early in 2006, in favor of Invirase boosted with ritonavir,[16] owing to the ability of the latter co-formulated drug to inhibit the enzyme that metabolizes the AIDS drugs.[citation needed]

Society and culture

Economics

As of 2015, it is not available as a generic medication.[17]

Formulations

Two formulations have been marketed:

  • a hard-gel capsule formulation of the mesylate, with trade name Invirase, which requires combination with ritonavir to increase the saquinavir bioavailability;
  • a soft-gel capsule formulation of saquinavir (microemulsion,[18] orally-administered formulation), with trade name Fortovase, which was discontinued worldwide in 2006.[19]

References

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  1. ^ Page Module:Citation/CS1/styles.css has no content."Saquinavir Use During Pregnancy". Drugs.com. 20 March 2018. Retrieved 28 January 2020.
  2. ^ Page Module:Citation/CS1/styles.css has no content.Roche Products Pty Limited (6 November 2018). "Invirase® (Saquinavir mesilate)". Australian Product Information. Archived from the original on 8 January 2023. Retrieved 8 January 2023 – via MedAdvisor International Pty Ltd.
  3. ^ Page Module:Citation/CS1/styles.css has no content."Invirase- saquinavir mesylate capsule INVIRASE- saquinavir mesylate tablet, film coated". DailyMed. 26 December 2019. Retrieved 28 January 2020.
  4. ^ a b c d e f g h i Page Module:Citation/CS1/styles.css has no content."Saquinavir". The American Society of Health-System Pharmacists. Archived from the original on 8 September 2015. Retrieved 5 September 2015.
  5. ^ Page Module:Citation/CS1/styles.css has no content.Minor LK (2006). Handbook of Assay Development in Drug Discovery. Hoboken: CRC Press. p. 117. ISBN 9781420015706. Archived from the original on 31 March 2016.
  6. ^ Page Module:Citation/CS1/styles.css has no content.Fischer J, Ganellin CR (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 509. ISBN 9783527607495.
  7. ^ Page Module:Citation/CS1/styles.css has no content."Fortovase". Drugs.com. 22 March 2019. Archived from the original on 28 April 2020. Retrieved 28 January 2020.
  8. ^ Page Module:Citation/CS1/styles.css has no content.Winston A, Back D, Fletcher C, Robinson L, Unsworth J, Tolowinska I, et al. (June 2006). "Effect of omeprazole on the pharmacokinetics of saquinavir-500 mg formulation with ritonavir in healthy male and female volunteers". AIDS. 20 (10): 1401–1406. doi:10.1097/01.aids.0000233573.41597.8a. PMID 16791014. S2CID 44506039.
  9. ^ Page Module:Citation/CS1/styles.css has no content.Dolin R, Masur H, Saag MS, eds. (1999). AIDS Therapy. Churchill Livingstone. p. 129. ISBN 9780443075926.
  10. ^ a b c Page Module:Citation/CS1/styles.css has no content.Centers for Disease Control and Prevention (CDC) (3 June 2011). "HIV Surveillance—United States, 1981-2008". Morbidity and Mortality Weekly Report. 60 (21): 689–693. PMID 21637182. Archived from the original on 9 November 2013. Retrieved 8 November 2013.
  11. ^ Page Module:Citation/CS1/styles.css has no content.Hilts PJ (8 December 1995). "F.D.A. Backs A New Drug To Fight AIDS". New York Times. Retrieved 28 October 2020.
  12. ^ Page Module:Citation/CS1/styles.css has no content."Antiretroviral Drug Discovery and Development". NIH. 26 November 2018. Retrieved 29 October 2020.
  13. ^ The CDC, in its Morbidity and Mortality Weekly Report, ascribes this to "highly active antiretroviral therapy", without mention of either of these drugs, see the preceding citation. A further citation is needed to make this accurate connection between this drop and the introduction of the protease inhibitors.
  14. ^ Page Module:Citation/CS1/styles.css has no content.AIDS Community Research Initiative of America. "Drugs! Drugs! Drugs! An Overview of the Approved Anti-HIV Medications". The Body. Archived from the original on 9 November 2013. Retrieved 20 February 2013.
  15. ^ Page Module:Citation/CS1/styles.css has no content."Drug Approval Package: Fortovase/Saquinavir NDA 20828". U.S. Food and Drug Administration (FDA). 24 December 1999. Archived from the original on 28 January 2020. Retrieved 28 January 2020.
  16. ^ Page Module:Citation/CS1/styles.css has no content."Withdrawal of Fortovase (PDF)" (PDF). Archived from the original (PDF) on 14 May 2006.
  17. ^ Page Module:Citation/CS1/styles.css has no content."Generic Invirase Availability". Drugs.com. Retrieved 9 July 2020.
  18. ^ Page Module:Citation/CS1/styles.css has no content.Gibaud S, Attivi D (August 2012). "Microemulsions for oral administration and their therapeutic applications" (PDF). Expert Opinion on Drug Delivery. 9 (8): 937–951. doi:10.1517/17425247.2012.694865. PMID 22663249. S2CID 28468973.
  19. ^ Page Module:Citation/CS1/styles.css has no content."Roche to discontinue the sale and distribution of Fortovase (saquinavir)". News-Medical.Net. 18 May 2005. Archived from the original on 22 February 2015.

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