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Dolutegravir
Clinical data
Trade namesTivicay, Tivicay PD, Instgra
Other namesGSK572, S-349572
AHFS/Drugs.comMonograph
MedlinePlusa613043
License data
Pregnancy
category
Routes of
administration		By mouth
ATC code
Legal status
Legal status
Pharmacokinetic data
Bioavailabilityn/a[4]
Protein binding≥98.9%
MetabolismUGT1A1 and CYP3A
Elimination half-life~14 hours
ExcretionFeces (53%) and urine (18.9%)
Identifiers
  • (4R,12aS)-N-(2,4-difluorobenzyl)-7-hydroxy-4-methyl-6,8-dioxo-3,4,6,8,12,12a-hexahydro-2H-pyrido[1',2':4,5]pyrazino[2,1-b] [1,3]oxazine-9-carboxamide
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
PDB ligand
CompTox Dashboard (EPA)
ECHA InfoCard100.237.735 Edit this at Wikidata
Chemical and physical data
FormulaC20H19F2N3O5
Molar mass419.385 g·mol−1
3D model (JSmol)
  • C[C@@H]1CCO[C@@H]2N1C(=O)c3c(c(=O)c(cn3C2)C(=O)NCc4ccc(cc4F)F)O
  • InChI=1S/C20H19F2N3O5/c1-10-4-5-30-15-9-24-8-13(17(26)18(27)16(24)20(29)25(10)15)19(28)23-7-11-2-3-12(21)6-14(11)22/h2-3,6,8,10,15,27H,4-5,7,9H2,1H3,(H,23,28)/t10-,15+/m1/s1 checkY
  • Key:RHWKPHLQXYSBKR-BMIGLBTASA-N checkY
 ☒NcheckY (what is this?)  (verify)

Dolutegravir (DTG), sold under the brand name Tivicay or Instgra, is an antiretroviral medication used, together with other medication, to treat HIV/AIDS.[6] It may also be used, as part of post exposure prophylaxis, to prevent HIV infection following potential exposure.[7] It is taken by mouth.[6]

Common side effects include trouble sleeping, feeling tired, diarrhea, high blood sugar, and headache.[7] Severe side effects may include allergic reactions and liver problems.[7] Concerns that usage during pregnancy can result in harm to the baby have been refuted by further studies that show there is no statistical difference in neural tube defects from the usage of dolutegravir compared to other antiretrovirals.[8] It is unclear if use during breastfeeding is safe.[7] Dolutegravir is an HIV integrase strand transfer inhibitor which blocks the functioning of HIV integrase which is needed for viral replication.[7]

Dolutegravir was approved for medical use in the United States in 2013.[7] It is on the World Health Organization's List of Essential Medicines.[9] Abacavir/dolutegravir/lamivudine, a combination with abacavir and lamivudine is also available.[7][10][11] As of 2019, the World Health Organization (WHO) recommends DTG as the first- and second-line treatment for all persons with HIV.[12]

Medical use

[edit]

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.[13]

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.[5]

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).[14]

Adverse effects

[edit]

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.[15] 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.[4]

Pregnancy

[edit]

In 2019 there were tentative concerns[16] that usage during pregnancy can result in the increased risk of neural tube defects however further studies have refuted that claim finding no statistical difference between dolutegravir and other antiretrovirals.[8] As of 31 January 2024[17] dolutegravir is the NIH preferred antiretroviral drug for pregnant or nonpregnant people trying to conceive.[18]

History

[edit]

In February 2013, the U.S. Food and Drug Administration (FDA) announced that it would fast track dolutegravir's approval process.[19] On 13 August 2013, dolutegravir was approved for medical use in the United States.[20] On 4 November 2013, dolutegravir was approved by Health Canada.[21] On 16 January 2014, it was approved by the European Commission for use throughout the European Union.[5]

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.[14] 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.[14][22]

The U.S. Food and Drug Administration (FDA) granted the approval of Tivicay and Tivicay PD to ViiV Healthcare.[14]

Access

[edit]

In April 2024, the government of Colombia issued its first ever compulsory license to invalidate the patent of Dolutegravir.[23][24] Access to dolutegravir was enabled by a license to the Medicines Patent Pool however Colombia was not a listed territory.[25] UNAIDS supported the move to enable a compulsory license decision.[26] ViiV Healthcare disagreed with the decision on the use of the compulsory license by the government of Colombia.[27] A separate agreement with the Medicines Patent Pool permits the distribution of generic versions of the medicine in Colombia, but this is restricted to children only.[28]

Climate change

[edit]

Dolutegravir, used by 24 million people in low- and middle-income countries, has significantly reduced carbon emissions compared to the previous standard of care, efavirenz.[29] This is the first report to analyze the environmental impact of a widely used medicine compared to its alternative. According to Unitaid, this transition will prevent over 26 million tons of CO2 from entering the atmosphere between 2017 and 2027, equivalent to eliminating 10 years of carbon emissions from Geneva, Switzerland.[30]

References

[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia

Dolutegravir

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Dolutegravir is an antiretroviral medication classified as an integrase strand transfer inhibitor (INSTI) used in for the treatment and prevention of HIV-1 infection. It functions by binding to the of the HIV integrase enzyme, thereby blocking the strand transfer step of retroviral DNA integration into the host cell genome, which is essential for . Developed through a collaboration between and —a involving GlaxoSmithKline—dolutegravir received initial U.S. FDA approval in 2013 for treatment-naïve adults, with subsequent expansions to broader populations including children and treatment-experienced patients based on phase III trials demonstrating superior viral suppression compared to alternatives like efavirenz-based regimens. Its high genetic barrier to resistance, unboosted once-daily oral dosing, and favorable pharmacokinetic profile have positioned it as a preferred first-line component in global HIV guidelines, contributing to improved outcomes in resource-limited settings. While generally well-tolerated, with common adverse effects including and , dolutegravir has been associated with benign elevations in serum creatinine due to tubular secretion inhibition and initial concerns over neural tube defects in infants exposed during conception—stemming from observational data in —but subsequent large-scale studies and meta-analyses have not confirmed a causal increase in such risks, leading to its endorsement by the WHO and others for use in with counseling.

Pharmacology

Mechanism of action

Dolutegravir functions as a second-generation integrase strand transfer inhibitor (INSTI), specifically targeting the HIV-1 integrase enzyme to block the strand transfer step of viral DNA integration into the host cell genome. By binding to the integrase active site, dolutegravir chelates the Mg²⁺ ions essential for catalysis, forming a stable complex that prevents the 3'-processing and subsequent strand transfer of proviral DNA. This inhibition occurs post-reverse transcription, halting the viral replication cycle at the integration phase without affecting host cellular processes. In comparison to first-generation INSTIs like raltegravir, dolutegravir exhibits markedly slower dissociation kinetics from integrase-DNA complexes, with dissociation half-lives exceeding 5 hours for both wild-type and mutant enzymes harboring substitutions at residues E92, Y143, Q148, or N155. This prolonged binding affinity enhances its potency, as demonstrated in biochemical assays where dolutegravir maintained inhibitory activity against integrase variants resistant to raltegravir, due to its ability to accommodate conformational changes in the binding pocket. In vitro studies confirm dolutegravir's efficacy against wild-type HIV-1 integrase, with IC₅₀ values in the nanomolar range for strand transfer inhibition, and retained activity against clinically relevant mutants that confer resistance to earlier INSTIs through reduced binding affinity. These findings underscore dolutegravir's targeted disruption of the intasome complex, the nucleoprotein assembly critical for viral DNA integration.

Pharmacokinetics

Dolutegravir is rapidly absorbed after , achieving median peak plasma concentrations (T_max) of 2 to 3 hours post-dose in the fasted state. Although absolute has not been established due to lack of intravenous data, its pharmacokinetic profile indicates efficient oral absorption. Administration with food enhances exposure, increasing the area under the plasma concentration-time curve (AUC) by 33% to 66% and maximum concentration (C_max) by 46% to 67%, while delaying T_max to 3 to 5 hours; these changes do not alter the recommended dosing, allowing administration with or without meals. The drug exhibits high of at least 98.9%, primarily to and alpha-1 acid glycoprotein, with an apparent of 17.4 L following a 50 mg dose. Dolutegravir is primarily metabolized in the liver via uridine diphosphate glucuronosyltransferase (UGT)1A1-mediated , with a minor role for (CYP)3A; the principal inactive metabolite is the ether . Elimination occurs mainly through , with approximately 53% of a radiolabeled dose recovered unchanged and 31% in (predominantly as metabolites, with <1% as unchanged drug), reflecting both biliary secretion and unabsorbed drug. The terminal elimination half-life is about 14 hours in healthy subjects (11 to 12 hours in HIV-infected individuals), and apparent oral clearance is 1.0 L/h, supporting once-daily dosing. In special populations, no dose adjustments are required for mild to moderate hepatic impairment (Child-Pugh A or B), where exposures are comparable to healthy subjects, though severe impairment (Child-Pugh C) has not been studied. For renal impairment, pharmacokinetics remain unchanged in mild to moderate cases (creatinine clearance ≥30 mL/min); in severe impairment or end-stage renal disease, AUC and C_max are reduced by about 40% and 23%, respectively, but no adjustment is recommended given the minimal renal excretion of unchanged drug (<1%). Population pharmacokinetic analyses in adults show no clinically significant influences from age, sex, race, or body weight.

Medical uses

Indications and regimens

Dolutegravir is indicated by the U.S. (FDA) for the treatment of human immunodeficiency virus type 1 () infection in adults and pediatric patients aged at least 4 weeks and weighing at least 3 kg, either treatment-naïve or treatment-experienced, always in combination with other antiretroviral agents. The (EMA) similarly approves dolutegravir in combination with other antiretrovirals for -infected adults and adolescents aged 12 years and older weighing at least 40 kg, with extensions to younger children via dispersible formulations for those weighing at least 3 kg from 4 weeks of age. The World Health Organization (WHO) has recommended dolutegravir-based regimens as the preferred first-line option for HIV treatment in adults since its 2016 guidelines, with the 2019 update extending this preference to all populations, including children, adolescents, and pregnant or breastfeeding women, following reviews of safety and programmatic data. Approved combination regimens include dolutegravir with (Dovato), a two-drug option for virologically suppressed adults and adolescents aged 12 years and older, as well as dolutegravir with and lamivudine (Triumeq) for broader pediatric and adult use. Dolutegravir is utilized in patients with multi-class resistance due to its high genetic barrier to resistance, particularly in integrase strand transfer inhibitor-naïve or experienced individuals without documented resistance to dolutegravir or raltegravir with sufficient dolutegravir dose adjustment. It is not indicated for HIV-2 infection, for which specific antiretroviral options differ due to inherent virologic distinctions, nor for acute HIV infection, as approvals focus on established chronic treatment.

Dosage and administration

Dolutegravir is available as 50 mg film-coated tablets for adults and older children, and as 5 mg or 10 mg scored dispersible tablets for oral suspension in younger pediatric patients. The dispersible tablets must be dispersed in a small volume of room-temperature water (typically 15-20 mL depending on the number of tablets) and administered immediately, with any remaining suspension discarded; they are not chewed, cut, or swallowed whole. No intravenous formulation exists, and administration is exclusively oral. For adults and adolescents weighing at least 40 kg who are antiretroviral-naïve or integrase strand transfer inhibitor (INSTI)-experienced without resistance, the recommended dose is 50 mg once daily, administered with or without food. In patients coadministered potent cytochrome P450 3A or UGT1A1 inducers such as efavirenz, fosamprenavir/ritonavir, tipranavir/ritonavir, or rifampin, the dose increases to 50 mg twice daily, with doses separated by approximately 12 hours. For INSTI-experienced patients with certain resistance mutations (e.g., Q148 with additional substitutions), a 50 mg twice-daily regimen may restore activity in optimized combination therapy, per U.S. Department of Health and Human Services guidelines. Pediatric dosing is weight-based and uses dispersible tablets for children under 40 kg:
Body Weight (kg)Recommended Dose
3 to <65 mg once daily (one 5-mg dispersible tablet)
6 to <1015 mg once daily (three 5-mg dispersible tablets)
10 to <1420 mg once daily (two 10-mg dispersible tablets)
14 to <2025 mg once daily (either two 10-mg and one 5-mg dispersible tablets or one 25-mg film-coated tablet if available)
20 to <4035 mg once daily (one 10-mg and three 5-mg dispersible tablets, or adjusted film-coated equivalents)
≥4050 mg once daily (one 50-mg film-coated tablet)
Dose adjustments are required for coadministration with inducers in pediatrics similar to adults. To minimize interactions, dolutegravir should be taken at least 2 hours before or 6 hours after antacids, laxatives, or supplements containing calcium, aluminum, magnesium, iron, or buffered formulations, as these reduce absorption. No routine dose adjustment is needed for mild to moderate hepatic impairment (Child-Pugh A or B) or mild to moderate renal impairment (creatinine clearance ≥30 mL/min), though monitoring is advised. Use is not recommended in severe hepatic impairment (Child-Pugh C) due to lack of data. In end-stage renal disease (creatinine clearance <15 mL/min or on dialysis), exposure may decrease by about 40%, warranting therapeutic drug monitoring if feasible.

Efficacy

Clinical trial evidence

The SINGLE trial evaluated dolutegravir (DTG) plus abacavir-lamivudine versus efavirenz plus tenofovir disoproxil fumarate-emtricitabine in 833 antiretroviral-naïve adults with HIV-1 infection. At 48 weeks, using FDA snapshot analysis, 88% of participants in the DTG arm achieved virologic suppression (HIV-1 RNA <50 copies/mL) compared to 81% in the efavirenz arm, meeting criteria for superiority (adjusted difference 7 percentage points; 95% CI, 2.6 to 11.5). Virologic failure rates were low (2% in DTG arm), with no resistance to integrase strand transfer inhibitors observed in treatment failures. In the SPRING-2 trial, a phase 3, double-blind study of 822 treatment-naïve adults, once-daily DTG (50 mg) combined with two nucleoside reverse transcriptase inhibitors was compared to twice-daily raltegravir (400 mg). At 48 weeks, 88% in the DTG group versus 85% in the raltegravir group achieved HIV-1 RNA <50 copies/mL (adjusted difference 2.5 percentage points; 95% CI, -2.2 to 7.4), confirming non-inferiority. Extended 96-week data maintained non-inferiority, with 81% suppression in both arms; confirmed virologic failures with resistance were fewer in the DTG arm (1 vs. 3 cases).70257-3/fulltext) The TANGO trial assessed switching 741 virologically suppressed adults from tenofovir alafenamide (TAF)-based triple therapy to DTG plus lamivudine fixed-dose combination versus continuing current regimens. At week 48, 93% in the switch arm maintained suppression (<50 copies/mL) versus 89% in the continuation arm (adjusted difference 3.4 percentage points; 95% CI, -1.0 to 7.7), demonstrating non-inferiority. Extensions through 144 weeks showed sustained suppression in 90% of the DTG/lamivudine group, with virologic failure in <2% and no integrase resistance mutations among failures, supporting long-term durability in switch settings.

Comparative advantages

Dolutegravir exhibits a higher genetic barrier to resistance compared to earlier integrase strand transfer inhibitors (INSTIs) such as raltegravir and , resulting in fewer virologic failures among treatment-experienced patients. In the phase III SAILING trial, dolutegravir plus an optimized background regimen achieved superior virologic suppression (79% vs. 70% at 24 weeks) relative to raltegravir in integrase inhibitor-naïve adults with virologic failure on prior therapies, with significantly lower rates of treatment-emergent resistance (2% vs. 10%).61121-0/fulltext) Meta-analyses of head-to-head trials confirm dolutegravir's advantage in durability, with reduced discontinuation due to virologic failure compared to these agents in both naïve and experienced populations. Relative to efavirenz, a non-nucleoside reverse transcriptase inhibitor (NNRTI), dolutegravir offers improved tolerability, particularly with fewer central nervous system adverse effects such as dizziness, insomnia, and neuropsychiatric symptoms. The SINGLE trial demonstrated dolutegravir's non-inferiority in virologic efficacy to efavirenz at 96 weeks while showing better overall safety, with lower rates of drug-related discontinuations (4% vs. 9%). Systematic reviews corroborate these findings, attributing dolutegravir's edge to its once-daily dosing and reduced toxicity profile, leading to higher treatment adherence in first-line settings. Compared to ritonavir-boosted protease inhibitors (PIs) like darunavir, dolutegravir provides equivalent or superior efficacy in treatment-naïve patients, alongside the convenience of unboosted, once-daily administration without food restrictions or pill burden from pharmacokinetic boosters. The FLAMINGO trial reported higher virologic response rates with dolutegravir (90% vs. 83% at 48 weeks) versus darunavir/ritonavir, with similar tolerability but advantages in lipid profile and dosing simplicity. Real-world cohort analyses further support dolutegravir's noninferiority to boosted PIs in viral suppression, with faster time to undetectability in some programmatic data, potentially lowering HIV transmission risk through earlier adherence to undetectable=untransmittable (U=U) thresholds.

Safety profile

Common adverse effects

The most common adverse effects associated with dolutegravir, observed in clinical trials such as GEMINI-1 and GEMINI-2, include headache (incidence of 3%), insomnia (2%), fatigue (2%), nausea (2%), and diarrhea (2%), primarily of mild (grade 1) intensity. These effects occurred at lower rates in dolutegravir plus lamivudine regimens compared to dolutegravir plus tenofovir disoproxil fumarate/emtricitabine (drug-related adverse events: 19.6% versus 25.0%). Discontinuation rates due to adverse effects remain low, at approximately 2-3% across treatment-naive populations in these phase 3 trials through 96 weeks, underscoring the drug's favorable tolerability profile. Weight gain is also reported, with mean increases of about 3 kg over 96 weeks in dolutegravir-containing regimens among antiretroviral-naive adults, a phenomenon linked to integrase strand transfer inhibitors as a class based on comparative trial data showing greater gains versus non-integrase inhibitors. Neuropsychiatric effects, such as insomnia and headache, are typically dose-dependent, mild, and resolve upon discontinuation.

Serious risks

Hypersensitivity reactions to dolutegravir occur infrequently, with an incidence of less than 1% in clinical trials and post-marketing reports, manifesting as rash accompanied by constitutional symptoms such as fever, and in severe cases, organ dysfunction including liver injury. Unlike abacavir-associated hypersensitivity, dolutegravir reactions are not linked to HLA-B*5701 allele status, necessitating prompt discontinuation upon suspicion and avoidance of rechallenge. Hepatotoxicity represents another serious risk, particularly in patients co-infected with hepatitis B or C viruses, where elevated transaminases, hepatitis, and rare instances of acute liver failure have been observed in both trials and post-marketing surveillance. The FDA prescribing information recommends baseline and periodic liver function monitoring in such individuals, with discontinuation advised if hepatotoxicity is confirmed. No black-box warnings apply to these risks apart from pregnancy-related counseling implemented prior to 2020.

Pregnancy outcomes

In 2018, preliminary data from the Botswana Tsepamo surveillance study reported neural tube defects (NTDs) in 4 of approximately 350 infants (rate of 0.9–1.1%) born to women receiving dolutegravir at conception, compared to a background rate of about 0.1% in the general population, prompting temporary regulatory warnings and WHO guidance against initiating dolutegravir in women of childbearing potential unless no alternatives existed. Follow-up analyses from Tsepamo, published in the New England Journal of Medicine in 2019, examined 1,683 deliveries with periconceptional dolutegravir exposure and identified 5 NTD cases (0.30% rate), which was lower than the initial signal but still elevated relative to background; a 2022 update on over 9,460 such exposures reported 10 NTDs (0.11% rate), aligning closely with expected population rates and not confirming a significant excess risk. A 2023 national cohort study in the United States, analyzing the largest dataset of periconceptional or early-pregnancy dolutegravir exposures (from Medicaid claims and other records spanning 2008–2020), found no NTD cases among 164 exposed pregnancies identified for detailed review, with overall NTD rates of 0.3% versus 0.2–0.4% in comparator antiretroviral therapy (ART) groups, providing no evidence of increased risk.00108-X/fulltext) Cumulative data from surveillance programs, including over 10,000 periconceptional dolutegravir exposures across Tsepamo and other registries like the Antiretroviral Pregnancy Registry, have not established a causal association with NTDs, as observed rates converge with background prevalence after accounting for confounding factors such as folate supplementation and HIV-related risks. Broader pregnancy outcomes, including preterm birth, low birth weight, and stillbirth, with dolutegravir-based regimens appear comparable to those with other integrase strand transfer inhibitors or standard ART, based on cohort comparisons adjusting for maternal HIV viral load and comorbidities.00108-X/fulltext) In response to accumulating evidence, the World Health Organization in July 2019 updated its guidelines to reinstate dolutegravir as the preferred first-line ART option for all populations, including pregnant women and those planning pregnancy, emphasizing its efficacy benefits while recommending preconception counseling on risks, effective contraception for non-pregnant individuals of childbearing potential, and folate supplementation.

Resistance and durability

Resistance mechanisms

Resistance to dolutegravir, an integrase strand transfer inhibitor (INSTI), primarily occurs via mutations in the HIV-1 pol gene encoding the integrase enzyme, disrupting the drug's binding to the integrase-DNA complex during viral strand transfer. Key resistance-associated mutations cluster at positions 140 (e.g., G140S or G140A), 148 (e.g., Q148H, Q148R, or Q148K), and 155 (e.g., N155H), with these often emerging in sequencing analyses from virologic failure cases. These mutations alter the catalytic core domain of integrase, reducing dolutegravir's affinity and inhibiting its ability to block 3'-processing and strand transfer steps in the viral lifecycle. Dolutegravir's high genetic barrier demands multiple concurrent or sequential mutations for clinically meaningful resistance, unlike first-generation INSTIs where single mutations suffice. Phenotypic susceptibility assays typically show that isolated primary mutations confer only modest fold-changes (e.g., 1.5- to 2-fold for R263K or N155H alone), but combinations such as Q148H/R/K plus G140S/A or additional accessory changes (e.g., E138K, T97A) yield >4-fold reductions, crossing thresholds for reduced susceptibility and enabling viral replication under drug pressure. This multi-hit requirement, evidenced in selections and patient-derived isolates, limits resistance emergence, particularly in integrase inhibitor-naïve individuals where rates remain below 1% across phase 3 trials and cohort studies. Cross-resistance patterns reflect shared binding sites among INSTIs: dolutegravir-resistant viruses with Q148 or N155 pathways exhibit high-level resistance to raltegravir (often >50-fold), driven by overlapping mutational impacts on the integrase active site. In contrast, activity against bictegravir is frequently retained against viruses with isolated raltegravir mutations due to dolutegravir's enhanced resistance profile, though complex profiles involving multiple second-generation INSTI mutations (e.g., Q148H/G140S plus N155H) confer extensive cross-resistance (>10-fold) to bictegravir and cabotegravir. Virologic pathways from failure cases underscore that resistance evolves via compensatory mutations restoring fitness, with integrase sequencing revealing associations like Q148 variants paired with G140S and S147G.

Factors influencing resistance

In treatment-experienced patients with HIV-1, particularly those with prior exposure to other integrase strand transfer inhibitors (INSTIs), the risk of dolutegravir resistance emergence is elevated due to pre-existing resistance-associated that reduce susceptibility. High baseline viral loads further exacerbate this risk, as observational studies link suboptimal virologic suppression at regimen initiation to increased selection pressure for resistant variants. Real-world data from cohort analyses confirm that poor adherence—defined as less than 95% adherence by pharmacy refill metrics—correlates strongly with treatment-emergent resistance, even in regimens with dolutegravir's high genetic barrier. In contrast, resistance rates remain low in INSTI-naïve patients initiating dolutegravir-based therapy, with first-line use showing rates under 0.5% in large-scale trials and real-world settings without failure.30036-2/fulltext) The DAWNING trial, evaluating second-line dolutegravir plus two inhibitors in 624 INSTI-naïve adults failing first-line non- regimens, reported virologic failure in 7.8% of the dolutegravir arm versus 15.6% in the lopinavir-ritonavir arm at 48 weeks, with no integrase resistance detected among dolutegravir failures. This underscores regimen context: dolutegravir's durability holds in multi-drug combinations but falters under monotherapy-like conditions. For salvage therapy in heavily treatment-experienced individuals, avoiding functional dolutegravir monotherapy is critical to mitigate resistance, as monotherapy selects for variants more rapidly than polytherapy. Combinations with boosted inhibitors, such as darunavir-ritonavir, enhance long-term virologic durability, with cohort studies showing sustained suppression in over 80% of highly experienced patients at 24-48 months without emergent integrase resistance.

Drug interactions

Key interactions

Dolutegravir is primarily metabolized by glucuronosyltransferase (UGT)1A1 and, to a lesser extent, (CYP)3A, making it susceptible to interactions with potent inducers of these enzymes. Coadministration with rifampin, a strong UGT1A1/CYP3A inducer, reduces dolutegravir area under the curve (AUC) by approximately 75% and maximum concentration (C_max) by 54%, as demonstrated in healthy volunteer pharmacokinetic studies. Similarly, carbamazepine, another potent inducer, decreases dolutegravir AUC by about 50% and C_max by 40% in dedicated interaction trials. Polyvalent cations such as magnesium, aluminum, calcium, and iron form chelates with dolutegravir, substantially impairing its absorption. Antacids containing aluminum or magnesium reduce dolutegravir AUC by up to 74% and C_max by 26% when administered simultaneously, per crossover studies in healthy subjects. Calcium- or iron-containing supplements similarly decrease exposure under fasted conditions, with reductions in AUC exceeding 50% observed in pharmacokinetic evaluations. Among antiretrovirals, dolutegravir exhibits minimal pharmacokinetic interactions with nucleoside/tide reverse transcriptase inhibitors (NRTIs), including emtricitabine/tenofovir (e.g., Truvada), allowing separate administration with dosing intervals without significant effects on absorption or efficacy. confirmed in studies combining it with abacavir-lamivudine or tenofovir-emtricitabine. Once-daily dosing for each permits flexible timing in HIV treatment or post-exposure prophylaxis (PEP) regimens, such as administering dolutegravir in the morning to mitigate potential insomnia. Non-nucleoside reverse transcriptase inhibitors (NNRTIs) generally show low interaction potential, though mild reductions in dolutegravir exposure (e.g., 10-20% AUC decrease with ) have been noted without in trial data. Boosted protease inhibitors, such as atazanavir/ritonavir or lopinavir/ritonavir, mildly increase dolutegravir AUC by 15-33% via CYP3A inhibition, as quantified in healthy volunteer and patient pharmacokinetic analyses.

Management strategies

Management of dolutegravir drug interactions focuses on pharmacokinetic adjustments to maintain therapeutic plasma concentrations, guided by clinical trials and expert panels. For strong inducers such as rifampin used in treatment, the recommended strategy is to increase dolutegravir to 50 mg twice daily during co-administration, as supported by pharmacokinetic studies demonstrating reduced dolutegravir exposure with once-daily dosing. This approach aligns with guidelines for -tuberculosis co-infection, prioritizing rifampin-based regimens while mitigating induction effects on dolutegravir metabolism via UGT1A1. In cases where dose adjustment is insufficient or not feasible, alternatives such as protease inhibitor-based regimens may be considered to avoid subtherapeutic levels. Therapeutic drug monitoring (TDM) is not routinely required for dolutegravir due to its favorable and high genetic barrier to resistance, but it may be beneficial in complex scenarios involving multiple interacting agents, virologic non-suppression, or pediatric patients to confirm adequate trough concentrations above 300 ng/mL. Guidelines from bodies like the U.S. Department of Health and Human Services emphasize TDM's utility in optimizing therapy when standard adjustments fail, rather than as a default practice. For interactions involving polyvalent cations or absorption inhibitors, management centers on temporal separation of doses—administering dolutegravir two hours before or six hours after such agents—to preserve , without need for routine plasma level checks in adherent adults. Patient counseling plays a key role, emphasizing consistent timing relative to interacting medications and adherence to adjusted regimens to prevent suboptimal exposure. In resource-limited settings, where co-infections like are prevalent, simplified strategies such as fixed-dose combinations with dose modifications are preferred to enhance feasibility, as evidenced by implementation data from high-burden regions. Overall, these evidence-based tactics minimize interaction risks while supporting dolutegravir's role in first- and second-line antiretroviral therapy.

History and development

Discovery and preclinical work

Dolutegravir, initially coded as S/GSK1349572, was discovered through a medicinal chemistry collaboration between Shionogi & Co., Ltd. and GlaxoSmithKline (GSK), focusing on next-generation HIV-1 integrase strand transfer inhibitors to address limitations of earlier agents like raltegravir. The lead optimization targeted tricyclic carbamoylpyridone scaffolds, incorporating a monoketone bioisostere to enhance binding affinity and metabolic stability, resulting in dolutegravir's distinctive pharmacophore that favored slower enzyme dissociation. This structural innovation stemmed from iterative structure-activity relationship studies in the mid-2000s, prioritizing potency against wild-type HIV-1 integrase while anticipating resistance mutations. In vitro preclinical evaluations highlighted dolutegravir's superior antiviral potency, with IC50 values in the low nanomolar range against raltegravir-resistant HIV-1 strains harboring primary mutations such as Y143R/C/H, Q148H/K/R, and N155H. Unlike raltegravir and elvitegravir, which showed marked shifts in susceptibility (up to >100-fold), dolutegravir retained near-wild-type activity due to its prolonged residence time on the integrase-DNA complex, as demonstrated by dissociation half-life measurements exceeding 70 hours compared to <1 hour for comparators. These findings underscored a causal advantage in barrier to resistance, informed by enzymatic and cell-based assays using patient-derived resistant isolates. Animal pharmacokinetic studies in rats and cynomolgus monkeys confirmed high oral of 75.6% and 87.0%, respectively, alongside extended plasma half-lives (approximately 13 hours in monkeys) that supported once-daily potential. Tissue distribution profiling revealed effective penetration into sanctuary sites like rectal and vaginal mucosa, with dolutegravir concentrations achieving 10- to 30-fold over plasma levels in these compartments relative to raltegravir, enhancing prospects for mucosal . No significant toxicity was observed in preclinical safety assessments across rodent and non-rodent species at exposures exceeding human equivalents. These data collectively advanced dolutegravir toward status by 2010.

Clinical development and approvals

Dolutegravir's clinical development featured pivotal Phase 3 trials establishing its efficacy as an integrase strand transfer inhibitor for HIV-1 treatment. The SINGLE trial (NCT01227352), completed in 2012, demonstrated superiority of dolutegravir plus abacavir/lamivudine over efavirenz/tenofovir/emtricitabine in treatment-naive adults, with 88% achieving viral load suppression below 50 copies/mL at 48 weeks compared to 81% in the control arm. SPRING-2 (NCT01227895) showed non-inferiority to twice-daily raltegravir in combination with two nucleoside reverse transcriptase inhibitors, achieving 88% and 81% suppression rates, respectively, at 48 weeks. For integrase inhibitor-experienced patients, VIKING-3 (NCT01328041) reported 63% achieving viral suppression at 24 weeks in those with raltegravir or elvitegravir resistance. These trials supported initial regulatory submissions, emphasizing dolutegravir's high barrier to resistance and once-daily dosing. The U.S. Food and Drug Administration (FDA) granted accelerated approval for dolutegravir as monotherapy (Tivicay) on August 12, 2013, for treatment-naive adults in combination with other antiretrovirals, based on virologic data with clinical benefit extrapolation from supporting trials. Full approval followed in 2014 after confirmatory data. The (EMA) authorized Tivicay on January 16, 2014, for similar indications in adults and adolescents over 30 kg. Combination products advanced rapidly: Triumeq (dolutegravir/abacavir/lamivudine) received FDA approval on August 22, 2014, and EMA authorization in September 2014, enabling single-tablet regimens for naive adults. Dovato (dolutegravir/lamivudine), a two-drug option, was FDA-approved on April 8, 2019, for treatment-naive adults with no prior virologic failure, supported by GEMINI trials showing 90% suppression at 48 weeks versus 93% for three-drug comparators. EMA approval followed on July 1, 2019. Pediatric expansions began in 2015 with FDA approval for children weighing at least 30 kg, extending to lower weights via dispersible formulations. On June 9, 2016, indications broadened to patients 12 years and older weighing 20-30 kg. By June 12, 2020, FDA approved Tivicay PD dispersible tablets for infants from four weeks old weighing at least 3 kg, based on IMPAACT P1093 pharmacokinetic data confirming to adult dosing. EMA followed with positive opinion in November 2020 for the 5 mg dispersible tablet in young children. The (WHO) included dolutegravir on its Model List of in 2014, designating it a preferred first-line option in 2016 guidelines for adults due to efficacy advantages over amid rising non-nucleoside resistance. Recommendations were reaffirmed in July 2019 for all populations, including pregnant women, following Botswana's Tsepamo study data alleviating concerns, with viral suppression rates exceeding 90% in real-world use.

Access and economics

Patent landscape and generics

Dolutegravir, marketed as Tivicay by (a of GlaxoSmithKline, , and ), is protected by primary patents on the expiring in 2027 and secondary patents on crystalline forms extending to 2029 in major markets such as the and . Combination formulations, such as abacavir/dolutegravir/lamivudine, are covered by additional patents lasting until 2031 in some jurisdictions. To facilitate earlier generic production in resource-limited settings, entered voluntary licensing agreements with the Medicines Patent Pool in April 2014, authorizing generic manufacturers to produce and supply dolutegravir-based regimens in at least 95 countries for adults and 123 for pediatric formulations. These agreements have been extended, including coverage for upper-middle-income countries like , , , and , enabling scaled-up generic supply without awaiting primary patent expiry. In , a key generic manufacturing hub, the rejected ViiV Healthcare's secondary patent application for dolutegravir on October 3, 2024, following oppositions citing lack of novelty and under Section 3(d) of India's Patents Act, thereby clearing the path for unrestricted domestic generic production. In the United States, the FDA has issued tentative approvals for eight generic versions of dolutegravir sodium tablets as of mid-2025, signaling but deferring final market entry pending and exclusivity resolutions, with the earliest potential launch projected for June 2030 barring challenges. Similar tentative approvals have been granted for generics, such as abacavir/dolutegravir/lamivudine by Lupin Pharmaceuticals in 2024 and 2025. These developments indicate accelerating generic competition post- expiry, particularly in low- and middle-income markets where voluntary licenses have already shifted supply toward lower-cost alternatives.

Global access and affordability

Following voluntary licensing agreements between and the in 2014, expanded to over 100 low- and middle-income countries (LMICs), generic manufacturers produced affordable dolutegravir-based regimens, primarily tenofovir/lamivudine/dolutegravir (TLD). These agreements facilitated price reductions from early LMIC offers around $75 per patient per year to under $45 per patient per year for TLD by 2023, as benchmarked by the Global Fund, driven by competition among generic suppliers. In , where prevalence is highest, dolutegravir rollout accelerated post-2018 WHO guidelines prioritizing integrase inhibitors, leading to TLD comprising the majority of first-line treatments in countries like by 2023.00047-4/fulltext) By late 2018, nearly 3.9 million people across developing countries had accessed generic dolutegravir or TLD, with sustained scale-up contributing to high viral suppression rates exceeding 90% in populations on the regimen. UNAIDS data indicate that expanded antiretroviral access, including dolutegravir's efficacy advantages over prior non-nucleoside inhibitor-based regimens, supported broader reductions in new infections, though specific attribution to dolutegravir varies by region and coincides with overall treatment scale-up. Persistent challenges in high-prevalence LMICs include vulnerabilities, such as errors and disruptions, which delayed initial introductions and risk stock-outs during rapid transitions. Adherence issues, exacerbated by socioeconomic factors and limited healthcare , further complicate equitable rollout, despite dolutegravir's once-daily dosing improving retention compared to earlier options. Early criticisms from access advocates highlighted delays in broad licensing and initial pricing above generic alternatives like efavirenz-based regimens (around $110–$184 per year), arguing these postponed adoption in resource-constrained settings until competitive pressures and WHO endorsement intervened.30154-0/abstract) Nonetheless, the model's scale has recouped innovation costs through high-income market revenues, enabling sustained LMIC affordability without compromising quality generics.

Environmental impact

Manufacturing emissions

Lifecycle assessments of dolutegravir production reveal a carbon footprint of approximately 223 grams of CO₂ equivalent per daily dose, based on a standard 50 mg tablet regimen. This equates to about 83 kilograms of CO₂e per patient-year, with emissions calculated across the full supply chain from raw materials to finished product. Nearly 90% of these emissions stem from active pharmaceutical ingredient (API) synthesis, which involves multi-step chemical processes yielding 27-52% efficiency and consuming substantial energy and solvents—estimated at 780,000 tons of solvents annually for global output. The API production emission factor stands at 314 kilograms of CO₂e per kilogram, reflecting the energy-intensive nature of reactions and waste generation in facilities often concentrated in regions like . By 2030, global dolutegravir production is forecasted to generate 2.6 million metric tons of CO₂e annually, equivalent to the total yearly emissions of a mid-sized city such as . Unitaid-supported initiatives aim to mitigate this through process optimizations, targeting up to 40% emission reductions via enhanced yields and integration, often at no added cost, alongside broader greening projected to cut impacts by 50% by 2040.

Net effects of adoption

The global transition to dolutegravir (DTG) as the preferred first-line antiretroviral for treatment has yielded a net reduction in carbon emissions relative to efavirenz-based regimens. A 2024 Unitaid report estimates that switching over 24 million patients from efavirenz to DTG between 2017 and 2027 averted approximately 26 million metric tons of CO2 equivalent emissions, equivalent to the annual footprint of a mid-sized city like for a decade. This stems from DTG's production being 2.6 times less carbon-intensive, attributable to its simpler synthesis requiring fewer chemical steps and less energy than efavirenz. These environmental gains occur without compromising clinical efficacy, as DTG exhibits higher rates of viral suppression and tolerability compared to , avoiding any inherent trade-off between therapeutic benefits and emissions. While pharmaceutical sector emissions constitute less than 5% of global health-related CO2 output—and a negligible share of total anthropogenic emissions—the data confirm verifiable, low-cost decarbonization from DTG adoption, supporting its sustained use alongside targeted green manufacturing optimizations to minimize residual impacts. Overemphasis on such sectoral footprints risks diverting focus from broader causal drivers of , yet the empirical reductions here align with first-line treatment imperatives prioritizing efficacy and scale.

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