|Trade names||Tivicay, Tivicay PD|
|Other names||GSK572, S-349572|
|Defined daily dose||50 mg|
|Metabolism||UGT1A1 and CYP3A|
|Elimination half-life||~14 hours|
|Excretion||Feces (53%) and urine (18.9%)|
|Chemical and physical data|
|Molar mass||419.38 g·mol−1|
|3D model (JSmol)|
|(what is this?)|
Dolutegravir (DTG), sold under the brand name Tivicay, is an antiretroviral medication used, together with other medication, to treat HIV/AIDS. It may also be used, as part of post exposure prophylaxis, to prevent HIV infection following potential exposure. It is taken by mouth.
Common side effects include trouble sleeping, feeling tired, diarrhea, high blood sugar, and headache. Severe side effects may include allergic reactions and liver problems. There is tentative concerns that use during pregnancy can result in harm to the baby. It is unclear if use during breastfeeding is safe. Dolutegravir is an HIV integrase strand transfer inhibitor which blocks the functioning of HIV integrase which is needed for viral replication.
Dolutegravir was approved for medical use in the United States in 2013. It is on the World Health Organization's List of Essential Medicines. In 2015, the cost of the medication in the United Kingdom was £499 per month. Abacavir/dolutegravir/lamivudine, a combination with abacavir and lamivudine is also available. As of 2019, the WHO recommends DTG as the first- and second-line treatment for all persons with HIV.
Dolutegravir is approved for use in a broad population of HIV-infected patients. It can be used to treat HIV-infected adults who have never taken HIV therapy (treatment-naïve) and HIV-infected adults who have previously taken HIV therapy (treatment-experienced), including those who have been treated with other integrase strand transfer inhibitors. Tivicay is also approved for children ages 12 years and older weighing at least 40 kilograms (kg) who are treatment-naïve or treatment-experienced but have not previously taken other integrase strand transfer inhibitors.
In the European Union it is indicated, in combination with other anti-retroviral medicinal products, for the treatment of Human Immunodeficiency Virus (HIV) infected adults, adolescents and children above six years of age.
In June 2020, the indication for dolutegravir in the US was updated to include children at least four weeks old and weighing at least 3 kg (6.61 pounds).
Common side effects of dolutegravir in clinical trials included insomnia and headache. Serious side effects included allergic reactions and abnormal liver function in patients who were also infected with hepatitis B or C. The package insert warns against a mean rise in serum creatinine of 0.11 mg/dL due to inhibition of tubular secretion of creatinine and does not affect GFR.
There is tentative concerns that use during pregnancy can result in harm to the baby. Effective birth control is thus recommended while on dolutegravir, with pregnancy testing before starting treatment. Use during the first trimester should only occur if there is no alternative.
In February 2013, the U.S. Food and Drug Administration (FDA) announced that it would fast track dolutegravir's approval process. On August 13, 2013, dolutegravir was approved for medical use in the United States. On November 4, 2013, dolutegravir was approved by Health Canada. On January 16, 2014, it was approved by the European Commission for use throughout the European Union.
In 2019, a triple-combination therapy, with dolutegravir replacing efavirenz, was introduced as the first-line treatment for all people (pregnant excluded) with HIV by the South African Government (public) sector.[medical citation needed]
In June 2020, dolutegravir was approved in the US with an indication to treat HIV-1 infection in children at least four weeks old and weighing at least 3 kg (6.61 pounds) in combination with other antiretroviral treatments. It is intended to treat children at least 4 weeks old and 3 kg who have never been treated for HIV or who have been treated, but not with an integrase strand transferase inhibitor (INSTI) class drug.
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- "Dolutegravir (Tivicay) Use During Pregnancy". Drugs.com. 16 October 2018. Retrieved 13 February 2020.
- "WHOCC - ATC/DDD Index". www.whocc.no. Retrieved 30 August 2020. CS1 maint: discouraged parameter (link)
- "Tivicay- dolutegravir sodium tablet, film coated". DailyMed. 24 October 2019. Retrieved 13 February 2020.
- British national formulary : BNF 69 (69 ed.). British Medical Association. 2015. p. 429. ISBN 9780857111562.
- "Dolutegravir Sodium Monograph for Professionals". Drugs.com. Retrieved 20 April 2019. CS1 maint: discouraged parameter (link)
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- "WHO recommends dolutegravir as preferred HIV treatment option in all populations". World Health Organization (Press release). Retrieved 2019-07-22.
- FDA approves new drug to treat HIV infection https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm364744.htm August 12, 2013[dead link]
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- "U.S. FDA approves GlaxoSmithKline's HIV drug Tivicay". Reuters. 12 August 2013. Retrieved 13 February 2020.
- "Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 1-4 October 2018". European Medicines Agency. 5 October 2018.
- "GSK wins priority status for new HIV drug in U.S". Reuters. 16 February 2013. Retrieved 18 February 2013. CS1 maint: discouraged parameter (link)[dead link]
- "Drug Approval Package: Tivicay (dolutegravir) Tablets NDA #204790". U.S. Food and Drug Administration (FDA). 13 September 2013. Retrieved 12 June 2020.
- "ViiV Healthcare receives approval for Tivicay (dolutegravir) in Canada for the treatment of HIV" (PDF). Archived from the original (PDF) on 12 November 2013. Retrieved 11 November 2013. CS1 maint: discouraged parameter (link)
- "ViiV Healthcare announces US FDA approval of the first-ever dispersible tablet formulation of dolutegravir, Tivicay PD, a once-daily treatment for children living with HIV". GSK (Press release). Retrieved 12 June 2020.