Detailed information

Darunavir (Prezista) is an antiretroviral drug from the class known as protease inhibitors. Protease inhibitors block the activity of the HIV protease enzyme that HIV uses to break up large viral proteins so that new HIV particles can be formed. Inhibiting this action slows HIV replication and delays damage to the immune system. Darunavir (formerly TMC114) was developed by the Belgian company Tibotec and designed to be active against HIV resistant to then-current 'first-generation' protease inhibitors. It was originally licensed in 2006 in the European Union and United States for use in highly treatment-experienced people.

The European Medicines Agency expanded its licence in 2008 to include use by people with any prior antiretroviral (ARV) experience.

In 2008, the US approved darunavir for use in previously untreated people, based on data from the ARTEMIS study. Approval for first-line use in Europe followed in February 2009.

Generic versions of darunavir have been approved in the European Union since 2018.


Darunavir/ritonavir is recommended as a preferred third agent for use in combination with tenofovir disoproxil fumarate and emtricitabine in first-line treatment in British HIV Association and US treatment guidelines.

Darunavir was initially licensed for treatment-experienced people on the basis of the POWER 1 and 2, phase IIb study results. In these studies, two different doses of boosted darunavir were compared with the effects of other protease inhibitors in treatment-experienced people. After a 24-week analysis, 600mg darunavir and 100mg ritonavir was selected as the optimal dose and all participants in the darunavir/ritonavir arm used that dosage.

Use of darunavir was approved at a dose of darunavir 600mg/ritonavir 100mg. (Clotet) (Lazzarin) Originally, darunavir's use in the EU was limited to highly treated adults who had failed more than one regimen containing a protease inhibitor. In 2008, its licensing was expanded to include any ARV-experienced person.

In 2008, the US Food and Drug Administration expanded the indication for darunavir to include its use as first-line therapy, dosed once daily. The protease inhibitor was also given full approval for twice-daily use in all people with previous ARV experience. This approval was based on data from the ARTEMIS study. 

In that study, results showed that people randomised to receive darunavir/ritonavir had a non-inferior virological response after 48 weeks as compared to those randomised to receive lopinavir/ritonavir (Kaletra). However, those who started treatment with a viral load over 100,000 copies/ml were significantly more likely to achieve a sustained undetectable viral load if they received darunavir/ritonavir. (Ortiz)

Darunavir was licensed in the US for use in treatment-naive people dosed as two 400mg tablets once daily with a 100mg boosting dose of ritonavir. In late 2008, once-daily dosing of boosted darunavir was approved in the US, dosed at darunavir 800mg/ritonavir 100mg, for a first-line regimen.



A combination of medications and the way it is taken.

boosting agent

Booster drugs are used to ‘boost’ the effects of protease inhibitors and some other antiretrovirals. Adding a small dose of a booster drug to an antiretroviral makes the liver break down the primary drug more slowly, which means that it stays in the body for longer times or at higher levels. Without the boosting agent, the prescribed dose of the primary drug would be ineffective.


A drug-resistant HIV strain is one which is less susceptible to the effects of one or more anti-HIV drugs because of an accumulation of HIV mutations in its genotype. Resistance can be the result of a poor adherence to treatment or of transmission of an already resistant virus.

viral load

Measurement of the amount of virus in a blood sample, reported as number of HIV RNA copies per milliliter of blood plasma. Viral load is an important indicator of HIV progression and of how well treatment is working. 



An essential organ involved in digestion of food and excretion of waste products from the body.

Darunavir/ritonavir has been compared with atazanavir/ritonavir, raltegravir and dolutegravir in two clinical trials in previously untreated people.

In the ACTG 5257 study people treated with raltegravir were significantly more likely to have undetectable viral load after 96 weeks when compared to atazanavir/ritonavir or darunavir/ritonavir, but also more likely to develop resistance after virological failure. (Lennox)

In the FLAMINGO study a significantly higher proportion of people who received dolutegravir plus two nucleoside reverse transcriptase inhibitors (NRTIs) had an undetectable viral load after 96 weeks compared to darunavir/ritonavir (80% vs 68%). The difference between arms was most pronounced in participants with high baseline viral load (> 100,000 copies/ml) (82% vs 52% response through week 96) and in people taking the tenofovir disoproxil fumarate/emtricitabine backbone (79% vs 64%). Virologic non-response to treatment (dolutegravir 8%; darunavir/ritonavir 12%) and non-response due to other reasons (dolutegravir 12%; darunavir/ritonavir 21%) occurred less frequently with dolutegravir. (Molina)

For ARV-experienced people, the TITAN study compared twice-daily darunavir/ritonavir (600mg/100mg) with twice-daily lopinavir/ritonavir capsules (at the previous 400mg/100mg formulation), plus an optimised background regimen selected by resistance testing.

After 48 weeks of treatment, intent-to-treat analysis showed that 77% of those randomised to receive darunavir had viral load below 400 copies/ml, compared with 68% of those randomised to receive lopinavir/ritonavir. This was statistically significant and darunavir/ritonavir was seen as having superiority over lopinavir/ritonavir in virologic suppression. A similar difference emerged when the proportion of people with viral load below 50 copies/ml at week 48 was compared. (Madruga) On the basis of this study, the drug was licensed for use in the EU for all ARV-experienced people.

Once-daily 800mg/100mg darunavir/ritonavir dosing is also suitable for some treatment-experienced people. The randomised, open-label ODIN trial found this once-daily dose to be as effective at suppressing viral load after 48 weeks as a 600mg twice-daily dose in treatment-experienced people who did not have resistance mutations to darunavir at the start of the trial. The once-daily dose was also less likely to cause lipid disturbances. (Cahn)

The open-label GRACE study found that 600/100mg darunavir/ritonavir twice daily, plus optimised background therapy, was equally effective in women and in men after 48 weeks. There was little difference in side effects, except that women were somewhat more likely to report nausea. (Currier)

A reduced dose of darunavir, boosted by ritonavir, was found to be effective in people switching treatment while virally suppressed. A randomised trial conducted in South Africa in 300 people found that switching to a 400mg/100mg daily dose of darunavir/ritonavir resulted in a similar rate of viral suppression as switching to lopinavir/ritonavir. (Venter)

Darunavir has also been tested as part of a two-drug regimen. The DUAL study tested switching to darunavir (boosted by ritonavir) and lamivudine in people with suppressed viral load on a three-drug regimen containing darunavir. After 48 weeks, people who were assigned to switch to the two-drug regimen had a similar rate of viral suppression to those who remained on the three-drug regimen. (Pulido)

The PROBE-2 study tested darunavir, boosted by cobicistat, and rilpivirine in people with suppressed viral load on a three-drug regimen. After 24 weeks, people who were assigned to switch to the two-drug regimen had a similar rate of viral suppression to those who remained on the three-drug regimen. Rilpivirine and darunavir/cobicistat was recommended as a new switch option in the 2019 European AIDS Clinical Society European treatment guidelines. (Maggiolo)

The DUALIS study tested switching to darunavir (boosted by ritonavir) and dolutegravir in people with suppressed viral load on a three-drug regimen containing boosted darunavir. (Spinner). After 48 weeks, people who were assigned to switch to the two-drug regimen had a similar rate of viral suppression to those who remained on the three-drug regimen. Dolutegravir and darunavir each have a high barrier to resistance and this regimen may be an appropriate switch option for people with limited treatment options due to drug resistance and/or poor tolerance for NRTIs.

Taking it

Darunavir is licensed in both the European Union and the US for use in both treatment-naive and treatment-experienced people. 

In November 2012, an 800mg tablet received US Food and Drug Administration approval and was approved in Europe in January 2013. This dosage is approved for previously untreated people, taken with 100mg of ritonavir.

Darunavir 800mg is also approved for use with a 150mg boosting dose of cobicistat. A fixed-dose tablet containing darunavir and cobicistat is also available. See Rezolsta for further details.

Treatment-experienced people should take 600mg twice daily boosted with ritonavir 100mg.

Darunavir is also available in a fixed-dose tablet combined with a 150mg boosting dose of cobicistat, 10mg of tenofovir alafenamide and 200mg of emtricitabine. See Symtuza for further details.

Darunavir should be taken with food.

Most drug-drug interaction studies used the twice-daily dose of boosted darunavir. Until more data are available, twice-daily dosing should be considered when darunavir is used with efavirenz, nevirapine, and etravirine in treatment-experienced people. However, in combination with raltegravir and maraviroc, once-daily dosing is an option. Neither lopinavir/ritonavir nor saquinavir is recommended for use with darunavir because of a significant decrease in darunavir serum concentration that occurs when these drugs are used together.  

Side effects

Common side effects of darunavir include elevated lipids, diabetes, insomnia, headache, dizziness, peripheral neuropathy, diarrhoea, nausea, vomiting and abdominal pain. Rash, itching, tiredness and fatigue are also common.

A caution has been issued by the European Medicines Agency and the US Food and Drug Administration regarding hepatic issues concerning darunavir. About 0.5% of people taking darunavir/ritonavir during its clinical development were diagnosed with drug-induced hepatitis. People with pre-existing liver problems, including hepatitis B or hepatitis C infection, had a greater risk of developing such a complication. No adjustment in the dose of darunavir/ritonavir is recommended for people with mild or moderate liver problems, but the US product label now notes that the drug is not recommended for people with severe liver problems.

Liver function should be monitored in all people before treatment with darunavir/ritonavir is started, and monitoring of ALT/AST levels should be increased in people with pre-existing liver problems during the first few months of therapy with the drug. If an individual experiences a worsening of their liver function, or if they develop symptoms suggestive of drug-induced hepatitis (tiredness, weight loss, nausea, yellowing of the skin, dark urine, pain in the liver, or an enlarged liver) doctors are recommended to consider either interrupting or stopping treatment with darunavir/ritonavir.

Weight gain after starting antiretroviral treatment has been observed in people with HIV. A US cohort study found that people treated with darunavir gained an average of 1kg per 6-month period on treatment. People receiving darunavir in this cohort gained more weight than people receiving any other regimen apart from the combination of dolutegravir, tenofovir alafenamide and emtricitabine. (Ruderman)


Development of resistance to darunavir is very rare; only four out of 3635 participants in clinical trials of darunavir developed a single protease inhibitor resistance mutation and only one lost susceptibility to the drug as a result of resistance. (Lathouwers)

Drug interactions

Darunavir (Prezista) is broken down through the cytochrome 3A4 system in the liver.

People taking darunavir should not take the following drugs:

  • Alfuzosin
  • Astemizole
  • Carbamazepine (Tegretol)
  • Cisapride
  • Colchicine in people with renal or hepatic impairment
  • Dihydroergotamine
  • Ergonovine
  • Ergotamine tartrate (Cafergot / Migril)
  • Hypericin (St John’s wort)
  • Lovastatin
  • Methylergonovine
  • Midazolam (Hypnovel)
  • Phenobarbital
  • Phenytoin (Epanutin)
  • Pimozide (Orap)
  • Rifampicin (Rifadin / Rimactane)
  • Simvastatin (Zocor)
  • Terfenadine
  • Triazolam.

The following drugs may require a dose adjustment in people taking darunavir, or may require darunavir’s dose to be altered. Until more data are available they should be used with darunavir cautiously:

  • Atorvastatin (Lipitor)
  • Bepidril
  • Ciclosporin (Neoral / Sandimmun)
  • Dexamethasone
  • Efavirenz (Sustiva)
  • Felodipine (Plendil)
  • Fluticasone propionate (Flixotide)
  • Indinavir (Crixivan)
  • Itraconazole (Sporanox)
  • Ketoconazole (Nizoral)
  • Lidocaine
  • Methadone hydrochloride (Methadose)
  • Nicardipine hydrochloride (Cardene / Cardene SR)
  • Nifedipine (Adalat / Adalat LA / Adalat Retard / Adipine MR / Adipine XL / Cardilate MR / Coracten SR / Coracten XL / Fortipine LA 40 / Hypolar Retard 20 / Nifedipress MR / Nifopress Retard / Slofedipine / Slofedipine XL / Tensipine MR)
  • Paroxetine (Seroxat)
  • Pravastatin sodium (Lipostat)
  • Rifabutin (Mycobutin)
  • Ritonavir-boosted lopinavir (Kaletra)
  • Quinidine sulphate
  • Sertraline (Lustral)
  • Sildenafil (Viagra), a reduced dose is recommended. Sildenafil is contraindicated if used for treatment of pulmonary arterial hypertension.
  • Sirolimus (Rapamune)
  • Tacrolimus (Prograf)
  • Tadalafil (Cialis), a reduced dose is recommended
  • Trazodone hydrochloride (Molipaxin)
  • Vardenafil (Levitra), a reduced dose is recommended
  • Voriconazole (Vfend)
  • Warfarin sodium.

Women using ethinylestradiol or norethidrone as hormonal contraception may experience reduced levels of the contraceptive if they take darunavir. Additional or alternative methods of contraception are recommended.

Darunavir should not be taken with the hepatitis C direct-acting antivirals elbasvir/grazoprevir (Zepatier), simeprevir (Olysio), paritaprevir, ombitasvir and dasabuvir (Viekirax). No dose adjustment of other direct-acting antivirals is necessary.


Darunavir is unsuitable for use in children below the age of 3. Dosing for children is determined by the child’s weight; the minimum weight required for treatment with darunavir/ritonavir is 10kg. Darunavir is available in liquid or tablet form and should be boosted with ritonavir tablets or liquid. Cobicistat is not recommended for use in children.


Darunavir/ritonavir should be used in pregnancy only if the benefits outweigh the risks. Lower blood levels of darunavir have been observed during pregnancy, implying a greater risk of treatment failure and subsequent drug resistance at this time. Darunavir boosted by cobicistat (in the products Rezolsta or Symtuza) is not recommended for use during pregnancy owing to lower blood levels after week 12 of pregnancy, increasing the risk of treatment failure and mother-to-child transmission of HIV.


Clotet B et al. Efficacy and safety of darunavir-ritonavir at week 48 in treatment-experienced patients with HIV-1 infection in POWER 1 and 2: a pooled subgroup analysis of data from two randomised trials. The Lancet, 369: 1169-1178, 2007.

Lazzarin A et al. TMC114 provides durable viral load suppression in treatment-experienced patients: POWER 1 and 2 combined 48 week analysis. 16th International AIDS Conference, Toronto, abstract TuAb0104, 2006.

Ortiz R et al. Efficacy and safety of once-daily darunavir/ritonavir versus lopinavir/ritonavir in treatment-naive HIV-1 infected patients at week 48. AIDS, 22: 1389-1397, 2008.

Lennox JL et al. Efficacy and tolerability of 3 nonnucleoside reverse transcriptase inhibitor-sparing antiretroviral regimens for treatment-naive volunteers infected with HIV-1: a randomized, controlled equivalence trial. Annals of Internal Medicine, 161: 461-471, 2014.

Molina J-M et al. Once-daily dolutegravir is superior to once-daily darunavir/ritonavir in treatment-naïve HIV-1-infected individuals: 96-week results from FLAMINGO (ING114915). International AIDS Society, 17: 6 (abstract 0153), 2014.

Madruga JV et al. Efficacy and safety of darunavir-ritonavir compared with that of lopinavir-ritonavir at 48 weeks in treatment-experienced, HIV-infected patients in TITAN: a randomised controlled phase III trial. The Lancet, 370: 49-58, 2007.

Cahn P et al. Efficacy and safety at 48 weeks of once-daily vs. twice-daily darunavir/ritonavir in treatment-experienced HIV-1-positive patients with no darunavir resistance-associated mutations: the ODIN Trial. 17th Conference on Retroviruses and Opportunistic Infections, abstract 57, San Francisco, 2010.

Currier J et al. Sex-based outcomes of darunavir-ritonavir therapy: a single-group trial. Annals of Internal Medicine, 153: 349-57, 2010.

Venter F et al. Non-inferior efficacy for darunavir/ritonavir 400/100mg once daily versus lopinavir/ritonavir, for patients with HIV RNA below 50 copies/mL in South Africa: the 48-week WRHI 052 study. 22nd International AIDS Conference (AIDS 2018), Amsterdam, abstract TUAB0107LB, 2018.

Pulido F et al. Dual therapy with darunavir and ritonavir plus lamivudine vs triple therapy with darunavir and ritonavir plus tenofovir disoproxil fumarate and emtricitabine or abacavir and lamivudine for maintenance of human immunodeficiency virus type 1 viral suppression: randomized, open-label, noninferiority Dual-GESIDA 8014-RIS-EST45 trial. Clinical Infectious Diseases, 65: 2112-2118, 2017.

Maggiolo F et al. Rilpivirine plus cobicistat-boosted darunavir as a two-drug switch regimen in HIV-infected, virologically suppressed subjects on steady standard three-drug therapy: a randomized, controlled, non-inferiority trial (PROBE 2). Journal of Antimicrobial Chemotherapy, 75: 1332-37, 2020.

Spinner C et al. Efficacy and safety of switching to dolutegravir with boosted darunavir in virologically suppressed adults with HIV-1: a randomized, open-label non-inferiority trial: the DUALIS study. Open Forum Infectious Diseases, 7: ofaa356, 2020.

Ruderman S et al. Weight gain following antiretroviral therapy (ART) initiation in ART-naïve people living with HIV in the current treatment era. Journal of Acquired Immune Deficiency Syndromes, 86: 339-342, 2021.

Lathouwers E et al. Pooled resistance analyses of darunavir once-daily regimens and formulations across 10 clinical studies of treatment-naïve and treatment-experienced patients with human immunodeficiency virus-1 infection. HIV Research & Clinical Practice, 21: 83-39, 2020.

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