Atazanavir
Other / unclassified targets UGT1A1 via inhibition
Regulatory milestones approvals, filings & regulatory actions · 11 recorded
| Milestone | Jurisdiction | Brand | Indication | Date | Sentence it was read from |
|---|---|---|---|---|---|
| Label expansions (9) | US (FDA) | REYATAZ | — | 2004-07-06 – 2017-05-23 | fda.gov ↗ |
| Approved | EU (EMA) | Reyataz | — | 2004-03-01 | europa.eu ↗ |
| Approved | US (FDA) | REYATAZ | — | 2003-06-20 | fda.gov ↗ |
Trials 109 · started per year
Also used as a comparator or background therapy in 81 trials
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 112 trials | ||||||
| Phase 1 | NCT02556268 Background | Feb → Dec 2016 | — | Bayer | Completed | No outcome recorded |
| Phase 1 | NCT01759875 Comparator | Jan 2013 → Jan 2014 | — | University of California, San Francisco | Completed | No outcome recorded |
| Phase 1 | NCT01404572 Comparator | Aug → Sep 2011 | HIV infectious disease | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 1 | NCT01458769 Comparator | Dec 2010 → Apr 2011 | — | Concert Pharmaceuticals | Completed | No outcome recorded |
| Phase 1 | NCT00833482 Comparator | Sep 2009 → Jul 2010 | HIV infectious disease | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 1 | NCT00646776 Comparator | Apr → Aug 2008 | — | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 1 | NCT00518297 Comparator | Aug → Dec 2007 | HIV infectious disease | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 1 | NCT00362726 Comparator | Sep → Nov 2006 | HIV infectious disease | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 1 | NCT00357188 Comparator | Jul → Sep 2006 | HIV infectious disease | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 1 | NCT00357240 Comparator | Jun → Aug 2006 | HIV infectious disease | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 1 | NCT00357721 Comparator | Jun → Sep 2006 | HIV infectious disease | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 1 | NCT00365339 Comparator | Apr → Jun 2006 | HIV infectious disease | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 1/21 trial | ||||||
| Phase 1/2 | NCT00411957 Comparator | Jan 2007 → Jan 2008 | HIV infectious disease | The HIV Netherlands Australia Thailand Research Collaboration | Completed | No outcome recorded |
| Phase 210 trials | ||||||
| Phase 2 | NCT06338826 Background | Feb 2025 → Sep 2027 expected | HIV infectious disease | ANRS, Emerging Infectious Diseases | Not yet recruiting | No outcome recorded |
| Phase 2 | NCT02116660 Comparator | Sep 2014 → Jul 2017 | HIV infectious disease | Merck Sharp & Dohme LLC | Terminated | No outcome recorded |
| Phase 2 | NCT01803074 Background | Apr 2013 → Nov 2014 | HIV infectious disease | ViiV Healthcare | Completed | No outcome recorded |
| Phase 2 | NCT01384734 Comparator | Jul 2011 → Feb 2013 | HIV infectious disease | ViiV Healthcare | Completed | No outcome recorded |
| Phase 2 | NCT00943540 Background | Jul 2009 → Dec 2010 | HIV infectious disease | Radboud University Medical Center | Completed | No outcome recorded |
| Phase 2 | NCT00892437 Background | May → Dec 2009 | HIV infectious disease | Gilead Sciences | Completed | No outcome recorded |
| Phase 2 | NCT00827112 Background | Mar 2009 → Jul 2010 | HIV infectious disease | ViiV Healthcare | Completed | No outcome recorded |
| Phase 2 | NCT00768989 Comparator | Nov 2008 → Jan 2010 | HIV infectious disease | Bristol-Myers Squibb | Terminated | No outcome recorded |
| Phase 2 | NCT00665847 Background | Nov 2008 → May 2011 | — | Tibotec Pharmaceuticals, Ireland | Completed | No outcome recorded |
| Phase 2 | NCT00122603 Background | Dec 2005 → Aug 2007 | HIV infectious disease | French National Agency for Research on AIDS and Viral Hepatitis | Completed | No outcome recorded |
| Phase 2/33 trials | ||||||
| Phase 2/3 | NCT02285114 Background | Jan 2015 → Nov 2019 | — | Gilead Sciences | Completed | No outcome recorded |
| Phase 2/3 | NCT01923311 Background | Aug 2013 → Nov 2017 | AIDS | Gilead Sciences | Terminated | No outcome recorded |
| Phase 2/3 | NCT03019783 Comparator | Dec 2011 → Jun 2015 | HIV infectious disease | Brigham and Women's Hospital | Completed | No outcome recorded |
| Phase 329 trials | ||||||
| Phase 3 | NCT03631732 Comparator | Aug 2018 → Aug 2019 | HIV infectious disease | Gilead Sciences | Completed | No outcome recorded |
| Phase 3 | NCT03256422 Background | Sep 2017 → Aug 2019 | HIV infectious disease | ANRS, Emerging Infectious Diseases | Completed | No outcome recorded |
| Phase 3 | NCT02616783 Comparator | Dec 2015 → Feb 2018 | HIV infectious disease | Gilead Sciences | Completed | No outcome recorded |
| Phase 3 | NCT02603107 Background | Nov 2015 → May 2017 | HIV infectious disease | Gilead Sciences | Completed | No outcome recorded |
| Phase 3 | NCT02605954 Comparator | Nov 2015 → Jun 2017 | HIV infectious disease | Gilead Sciences | Completed | No outcome recorded |
| Phase 3 | NCT02469246 Background | Jun 2015 → Dec 2017 | HIV infectious disease | Gilead Sciences | Completed | No outcome recorded |
| Phase 3 | NCT02397096 Background | Jun 2015 → Feb 2018 | HIV infectious disease | Merck Sharp & Dohme LLC | Completed | No outcome recorded |
| Phase 3 | NCT02269917 Comparator | Mar 2015 → Feb 2017 | HIV infectious disease | Janssen R&D Ireland | Completed | No outcome recorded |
| Phase 3 | NCT02302547 Comparator | Dec 2014 → Aug 2017 | HIV infectious disease | University Hospital, Tours | Completed | No outcome recorded |
| Phase 3 | NCT02157311 Background | Jul 2014 → Jan 2016 | HIV infectious disease | ANRS, Emerging Infectious Diseases | Completed | No outcome recorded |
| Phase 3 | NCT02121795 Background | May 2014 → Aug 2015 | HIV infectious disease | Gilead Sciences | Completed | No outcome recorded |
| Phase 3 | NCT02155101 Comparator | May 2014 → Jun 2016 | HIV infectious disease | University of Liverpool | Completed | No outcome recorded |
| Phase 3 | NCT01967940 Background | Oct 2013 → May 2015 | AIDS | Gilead Sciences | Completed | No outcome recorded |
| Phase 3 | NCT01910402 Comparator | Aug 2013 → Sep 2015 | HIV infectious disease | ViiV Healthcare | Completed | No outcome recorded |
| Phase 3 | NCT01815736 Comparator | Mar 2013 → Mar 2015 | HIV infectious disease | Gilead Sciences | Completed | No outcome recorded |
| Phase 3 | NCT01620944 Background | Jul 2012 → Jan 2013 | HIV infectious disease | Bristol-Myers Squibb | Terminated | No outcome recorded |
| Phase 3 | NCT01475838 Comparator | Nov 2011 → Nov 2013 | AIDS | Gilead Sciences | Completed | No outcome recorded |
| Phase 3 | NCT01363011 Background | May 2011 → Jan 2013 | AIDS | Gilead Sciences | Completed | No outcome recorded |
| Phase 3 | NCT01252940 Background | Nov 2010 → Jan 2012 | HIV infectious disease | Gilead Sciences | Completed | No outcome recorded |
| Phase 3 | NCT01106586 Comparator | Apr 2010 → Sep 2011 | HIV infectious disease | Gilead Sciences | Completed | No outcome recorded |
| Phase 3 | NCT01108510 Background | Apr 2010 → Nov 2011 | HIV infectious disease | Gilead Sciences | Completed | No outcome recorded |
| Phase 3 | NCT00874523 Comparator | Jul 2009 → Jul 2011 | HIV infectious disease | Kirby Institute | Completed | No outcome recorded |
| Phase 3 | NCT00708162 Background | Jul 2008 → Dec 2010 | HIV infectious disease | Gilead Sciences | Completed | No outcome recorded |
| Phase 3 | NCT00389207 Comparator | Oct 2006 → Feb 2011 | HIV infectious disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT00272779 Comparator | Nov 2005 → Jun 2007 | HIV infectious disease | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 3 | NCT00135395 Comparator | May 2004 → Feb 2006 | HIV infectious disease | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 3 | NCT00120393 Comparator | Jan 2004 → May 2006 | HIV infectious disease | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 3 | NCT00067782 Comparator | Dec 2002 → Mar 2005 | HIV infectious disease | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 3 | NCT00035932 Comparator | Nov 2001 → Jul 2003 | HIV infectious disease | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 421 trials | ||||||
| Phase 4 | NCT01902186 Background | Sep 2014 → Dec 2016 | HIV infectious disease | Giovanni Di Perri | Terminated | No outcome recorded |
| Phase 4 | NCT01829802 Background | May 2014 → Oct 2017 | HIV infectious disease | Pedro Cahn | Unknown | No outcome recorded |
| Phase 4 | NCT01599364 Background | Apr 2014 → Apr 2016 | HIV infectious disease | Catholic University of the Sacred Heart | Completed | No outcome recorded |
| Phase 4 | NCT01691794 Comparator | Nov 2012 → Oct 2014 | — | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 4 | NCT01637259 Comparator | Jun 2012 → Dec 2015 | HIV infectious disease, proteinuria | Kirby Institute | Completed | No outcome recorded |
| Phase 4 | NCT01332227 Background | Oct 2011 → Sep 2013 | — | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 4 | NCT01307488 Background | Sep 2011 → Apr 2014 | HIV infectious disease | Fundacion SEIMC-GESIDA | Completed | No outcome recorded |
| Phase 4 | NCT01225705 Comparator | Oct 2010 → Aug 2012 | HIV infectious disease, hepatitis C virus infection | University Hospital, Bonn | Withdrawn | No outcome recorded |
| Phase 4 | NCT01105611 Comparator | Aug 2010 → Dec 2012 | HIV infectious disease, hepatitis C virus infection | St. James's Hospital, Ireland | Unknown | No outcome recorded |
| Phase 4 | NCT01102972 Comparator | Apr 2010 → Jun 2012 | HIV infectious disease | ViiV Healthcare | Completed | No outcome recorded |
| Phase 4 | NCT00762892 Comparator | Jan 2009 → Dec 2012 | HIV infectious disease | The University of Texas Health Science Center, Houston | Completed | No outcome recorded |
| Phase 4 | NCT00544128 Comparator | Oct 2007 → Feb 2012 | HIV infectious disease | International Medical Center of Japan | Completed | No outcome recorded |
| Phase 4 | NCT00552240 Comparator | Sep 2007 → Mar 2010 | HIV infectious disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 4 | NCT00540137 Comparator | Jul 2007 → Dec 2012 | HIV infectious disease | Imperial College London | Completed | No outcome recorded |
| Phase 4 | NCT00335322 Comparator | Feb 2007 → Mar 2011 | HIV infectious disease | Kirby Institute | Completed | No outcome recorded |
| Phase 4 | NCT00384904 Comparator | Dec 2006 → Dec 2007 | HIV infectious disease | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 4 | NCT01388543 Comparator | Sep 2006 → Jun 2008 | HIV infectious disease | University of Colorado, Denver | Completed | No outcome recorded |
| Phase 4 | NCT00135356 Comparator | Jul 2005 → Jul 2007 | AIDS dysmorphic syndrome | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 4 | NCT00084253 Comparator | Jun 2004 → Aug 2006 | HIV infectious disease | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 4 | NCT00242216 Comparator | May 2004 → Mar 2010 | HIV infectious disease | The University of Texas Health Science Center, Houston | Completed | No outcome recorded |
| Phase 4 | NCT01445223 Comparator | Apr 2004 → Dec 2009 | HIV infectious disease | Göteborg University | Completed | No outcome recorded |
| Phase not applicable5 trials | ||||||
| — | NCT05044962 Comparator | Nov 2021 → Mar 2027 expected | HIV infectious disease | University of Alabama at Birmingham | Recruiting | No outcome recorded |
| — | NCT00916448 Comparator | May 2009 → Mar 2010 | infectious disease with sepsis, multiple organ dysfunction syndrome | Radboud University Medical Center | Completed | No outcome recorded |
| — | NCT02102048 Comparator | Jan 2009 → Mar 2014 | HIV infectious disease | University of Roma La Sapienza | Unknown | No outcome recorded |
| — | NCT00413153 Comparator | May 2006 → Dec 2008 | HIV infectious disease | Massachusetts General Hospital | Completed | No outcome recorded |
| — | NCT00192608 Background | Nov 2004 → May 2006 | HIV infectious disease | Kirby Institute | Completed | No outcome recorded |
Press releases naming this drug 1 release
| Date | Issuer | Release |
|---|---|---|
| 2017-12-27 | Teva Branded Pharmaceutical Products R&D, Inc. | Teva Announces Exclusive Launch of a Generic Version of Reyataz® in the United States tevapharm.com ↗ |
Evidence & citations 26 cited values
Every value below carries the sentence it was read from. 200 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | atazanavir | “Generic names: Efavirenz/Emtricitabine/Tenofovir, Lamivudine/Zidovudine, Emtricitabine, Lamivudine, Abacavir/Lamivudine, Zidovudine, Abacavir/Lamivudine/Zidovudine,...” NCT00624195 ↗182“Additional ARVs provided for use in this study included fixed dose combination lamivudine/zidovudine (3TC/ZDV), lamivudine (3TC), zidovudine (ZDV), tenofovir (TDF), fixed dose...” NCT00955968 ↗ “Participants stayed on their baseline emtricitabine (FTC)/tenofovir disoproxil fumarate (TDF)-containing regimen E/C/F/TDF; efavirenz (EFV)/FTC/TDF; ritonavir (RTV)-boosted...” NCT01815736 ↗ “Following the washout period, all participants who received TAF in Part 1 and have a \> 0.5 log10 decline in HIV-1 RNA will receive...” NCT01967940 ↗ “ART that concurrently contains combinations of non-nucleoside reverse transcriptase inhibitors (NNRTIs), such as efavirenz, and protease-inhibitors (PIs), such as...” NCT05044962 ↗ “This 48-week randomized study examined the safety and efficacy of a switch in CART to a once-daily regimen of saquinavir (SQV), ritonavir (RTV), and atazanavir (ATV) that did...” PMID 17479946 ↗ Apr 2007 “Baseline regimen of antiretroviral therapy with a ritonavir- or cobicistat-boosted protease inhibitor (atazanavir, darunavir, or lopinavir) administered according to the...” NCT02397096 ↗ “The preferentially recommended treatment of the study is atazanavir boosted with ritonavir, associated with a fixed combination of abacavir and lamivudine or emtricitabine + tenofovir” NCT00820118 ↗ “Boosted protease inhibitor (limited to darunavir \[DRV\] or atazanavir with low-dose ritonavir \[rtv\] or cobicistat \[COBI\], or lopinavir with rtv) as per current treatment regimen.” NCT02269917 ↗ “Tenofovir+Emtricitabine+Third agent (Including a ritonavir-boosted protease inhibitor : saquinavir or indinavir or fosamprenavir or tipranavir or darunavir or atazanavir or lopinavir” NCT02302547 ↗ “Any approved antiretroviral protease inhibitor such as atazanavir, darunavir, indinavir, ritonavir, and saquinavir ; consistent with the most recent prescribing information documents” NCT02556268 ↗ “(Fosamprenavir, atazanavir, lopinavir or darunavir) boosted with 100 mg of ritonavir, or atazanavir (400 mg / d) not boosted with ritonavir,if the 2 NRTIs are abacavir + Lamivudine” NCT02513147 ↗ “We enrolled women with HIV who were either ART-naive (control group; n=25), receiving efavirenz-based ART (n=25), or receiving atazanavir-ritonavir-based ART (n=24).” PMID 31498109 ↗ Sep 2019 “Atazanavir (300 mg once daily) and lopinavir (400 mg twice daily), each with low-dose ritonavir, achieved similar IQs in HIV-infected, treatment-naive patients.” PMID 22121190 ↗ Nov 2011 “Protease inhibitors (PIs) included amprenavir, atazanavir, darunavir, fosamprenavir, Kaletra (lopinavir/ritonavir, coformulated), ritonavir, and saquinavir.” NCT01252940 ↗ “Study of Cobicistat-Boosted Atazanavir (ATV/co), Cobicistat-Boosted Darunavir (DRV/co) and Emtricitabine/Tenofovir Alafenamide (F/TAF) in Children With HIV” NCT02016924 ↗ “atazanavir 300 mg and ritonavir 100 mg once daily or lopinavir 400 mg and ritonavir 100 mg twice daily plus two NRTIs; boosted protease inhibitor group” PMID 40883049 ↗ Sep 2025 “Participants receiving lopinavir/ritonavir (LPV/r) or atazanavir/ritonavir (ATV/r) as part of their background regimen will receive EVG 85 mg” NCT00708162 ↗ “PIs used as study drugs will include atazanavir (+/- ritonavir), fosamprenavir (+/-ritonavir), lopinavir/ritonavir, and darunavir/ritonavir.” NCT00884793 ↗ “switch the protease inhibitor for oral atazanavir 200 mg and ritonavir 100 mg or for atazanavir 300 mg and ritonavir 100 mg once daily” PMID 27470026 ↗ May 2016 “Patients on second line antiretroviral therapy take 2 NRTIs and either protease inhibitor lopinavir/ritonavir or atazanavir/ritonavir.” NCT02155101 ↗ “allowed PIs include atazanavir (ATV), darunavir (DRV), fosamprenavir (FPV), lopinavir (LPV), or saquinavir (SQV)” NCT01475838 ↗ “We investigated whether dose escalation of atazanavir/ritonavir could safely overcome the DDI with rifampicin.” PMID 37982585 ↗ May 2024 “maraviroc (Selzentry, Celsentri) 150mg QD + atazanavir (Reyataz) /ritonavir (Norvir) (300/100mg) QD” NCT00827112 ↗ “Either Once Daily Atazanavir/Ritonavir (ATV/r) or Once Daily Darunavir/Ritonavir (DRV/r)” NCT00756730 ↗ “Novel Protease Inhibitor (BMS 232632, Atazanavir, ATV, Reyataz) in Combination Regimens” NCT00006604 ↗ “allowed boosted 3rd ARV agents: lopinavir (LPV), atazanavir (ATV), darunavir (DRV)” NCT02285114 ↗ “atazanavir 300mg + ritonavir 100mg + tenofovir 300mg/emtricitabine 200mg” NCT01102972 ↗ “Atazanavir (ATV) 300 mg capsule administered orally once daily” NCT01108510 ↗ “Atazanavir (ATV) 300 mg capsule administered orally once daily” NCT00892437 ↗ “Atazanavir (ATV) 400 mg tablet administered orally once daily” NCT01565889 ↗ “ritonavir (RTV)-boosted atazanavir (ATV) or darunavir (DRV)” PMID 25397568 ↗ Nov 2014 “Atazanavir 300 mg capsule administered orally once daily” NCT01106586 ↗ “atazanavir (ATV; Reyataz®) + ritonavir (RTV; Norvir®)” NCT02616783 ↗ “atazanavir (ATV; Reyataz®) + ritonavir (RTV; Norvir®)” NCT02605954 ↗ “Ritonavir-boosted Atazanavir Plus Abacavir/Lamivudine” NCT02246998 ↗ “boosted atazanavir (ATV) or darunavir (DRV)” NCT02603107 ↗ “Atazanavir + Fosamprenavir + ritonavir” NCT00122603 ↗ “ritonavir-boosted atazanavir (ATV/r)” NCT02121795 ↗ “atazanavir 300mg + cobicistat 150mg” NCT02589158 ↗ “atazanavir (ATV) + ritonavir (RTV)” NCT02469246 ↗ “PI/r = atazanavir/r ou darunavir/r” NCT06338826 ↗ “boosted atazanavir (ATV)” NCT06337032 ↗ “atazanavir 300 mg daily” NCT01367236 ↗ “atazanavir (ATV)” NCT03631732 ↗ “atazanavir [ATV]” NCT00665847 ↗ “atazanavir” NCT01637259 ↗ |
| Known as | Atazanavir (as sulfate) | ChEMBL registry synonym — accepted as the source's own label CHEMBL1163 ↗ |
| Known as | atazanavir (Reyataz, ATV) | “atazanavir (Reyataz, ATV)” NCT00884793 ↗ |
| Known as | Atazanavir krka | ChEMBL registry synonym — accepted as the source's own label CHEMBL1163 ↗ |
| Known as | Atazanavir mylan | ChEMBL registry synonym — accepted as the source's own label CHEMBL1163 ↗ |
| Known as | Atazanavir so4 | ChEMBL registry synonym — accepted as the source's own label CHEMBL1163 ↗ |
| Known as | ATAZANAVIR SULFATE | ChEMBL registry synonym — accepted as the source's own label CHEMBL1163 ↗ |
| Known as | Atazanavir sulfate component of evotaz | ChEMBL registry synonym — accepted as the source's own label CHEMBL1163 ↗ |
| Known as | Atazanavir Sulphate | “Drug: Atazanavir Sulphate” NCT00357721 ↗1“Drug: Atazanavir Sulphate” NCT01335698 ↗ |
| Known as | Atazanavir viatris (previously atazanavir mylan) | ChEMBL registry synonym — accepted as the source's own label CHEMBL1163 ↗ |
| Known as | Atazanavir-ritonavir | “Atazanavir-ritonavir” NCT01231685 ↗ |
| Known as | atazanavir/r | “Background regimen may consist of the following ritonavir (RTV)-boosted PIs (PI/r): lopinavir/r (Kaletra), atazanavir/r, darunavir/r, tipranavir/r, or fosamprenavir/r.” NCT01923311 ↗2“protease inhibitors : lopinavir/r, darunavir/r ou atazanavir/r” NCT03256422 ↗ “atazanavir/r” NCT02157311 ↗ |
| Known as | Atazanaviri sulfas | ChEMBL registry synonym — accepted as the source's own label CHEMBL1163 ↗ |
| Known as | Atazor | ChEMBL registry synonym — accepted as the source's own label CHEMBL1163 ↗ |
| Known as | ATV | “Additional ARVs provided for use in this study included fixed dose combination lamivudine/zidovudine (3TC/ZDV), lamivudine (3TC), zidovudine (ZDV), tenofovir (TDF), fixed dose...” NCT00955968 ↗39“This 48-week randomized study examined the safety and efficacy of a switch in CART to a once-daily regimen of saquinavir (SQV), ritonavir (RTV), and atazanavir (ATV) that did...” PMID 17479946 ↗ Apr 2007 “Concurrent atazanavir (ATV) and lopinavir/ritonavir (LPV/r) may be useful for patients with extensive antiretroviral resistance; however, limited information exists concerning...” PMID 19906626 ↗ Sep 2009 “The purpose of this study is to determine whether two drugs, atazanavir (ATV) and ritonavir (RTV), will control HIV infection when taken together without any other anti-HIV...” NCT00084019 ↗ “We therefore evaluated the PK profiles of lower than the standard doses of atazanavir/ritonavir (ATV/RTV) in 22 adult Thai patients with well-suppressed human immunodeficiency...” PMID 19118378 ↗ Dec 2008 “Atazanavir (ATV) 300 mg taken by mouth following a meal each morning for 2 weeks during the Pre-Treatment Period and for 48 weeks during the Treatment Period.” NCT00896051 ↗ “receive abacavir sulfate/lamivudine/zidovudine (ABC/3TC/ZDV) twice-daily or atazanavir (ATV) once-daily plus lamivudine/zidovudine (3TC/ZDV) twice-daily.” PMID 19358725 ↗ Apr 2009 “Cobicistat (COBI) enhances atazanavir (ATV) pharmacokinetic parameters similarly to ritonavir (RTV) in both healthy volunteers and HIV-infected adults.” PMID 27774892 ↗ 2017 “To assess safety and efficacy of a switch to unboosted atazanavir (ATV) among HIV-infected adults receiving ATV/ritonavir (r) and tenofovir” PMID 28067119 ↗ Jan 2017 “the antiretroviral drug atazanavir (ATV) increases bilirubin levels but may also increase von Willebrand factor levels.” PMID 29023508 ↗ Oct 2017 “combination of Raltegravir (RAL) 400mg BID + Atazanavir (ATV) 300 mg BID in Antiretroviral (ARV)-experienced subjects” NCT00814879 ↗ “Atazanavir (ATV) + ritonavir (RTV), continuation of backbone 2 nucleoside reverse transcriptase inhibitor (NRTIs)” NCT00135356 ↗ “allowed PIs include atazanavir (ATV), darunavir (DRV), fosamprenavir (FPV), lopinavir (LPV), or saquinavir (SQV)” NCT01475838 ↗ “Comparison Atazanavir/Ritonavir (ATV/r) vs Nevirapine (NVP) Twice a Day (Bid) on Truvada Backbone” NCT00552240 ↗ “Novel Protease Inhibitor (BMS 232632, Atazanavir, ATV, Reyataz) in Combination Regimens” NCT00006604 ↗ “experimental atazanavir [ATV] dose 300 mg bid + raltegravir [RAL] 400 mg bid [ATV+RAL]” PMID 22592092 ↗ May 2012 “ritonavir-boosted (RTV) protease inhibitor regimen of atazanavir (ATV)/RTV+FTC/TDF” PMID 22748590 ↗ Jun 2012 “allowed boosted 3rd ARV agents: lopinavir (LPV), atazanavir (ATV), darunavir (DRV)” NCT02285114 ↗ “Abacavir (ABC)/lamivudine (3TC) + atazanavir (ATV) + ritonavir (/r)” NCT00440947 ↗ “Atazanavir (ATV) 300 mg capsule administered orally once daily” NCT00892437 ↗ “received atazanavir (ATV), 150 mg, and ritonavir (RTV), 80 mg” NCT01099579 ↗ “Atazanavir (ATV) 400 mg tablet administered orally once daily” NCT01565889 ↗ “plasma levels of atazanavir (ATV) may be higher in Koreans” NCT01368783 ↗ “atazanavir (ATV; Reyataz®) + ritonavir (RTV; Norvir®)” NCT02616783 ↗ “atazanavir (ATV; Reyataz®) + ritonavir (RTV; Norvir®)” NCT02605954 ↗ “Atazanavir (ATV) Powder Boosted With Ritonavir (RTV)” NCT01335698 ↗ “the recently developed drug atazanavir (ATV)” NCT00389402 ↗ “boosted atazanavir (ATV) or darunavir (DRV)” NCT02603107 ↗ “ritonavir (RTV)-boosted atazanavir (ATV/r)” NCT02246998 ↗ “atazanavir plus ritonavir (ATV+RTV)” NCT01910402 ↗ “atazanavir (ATV) + ritonavir (RTV)” NCT02469246 ↗ “Atazanavir (ATV) 300 mg tablets” NCT02116660 ↗ “1. Atazanavir (ATV)” NCT04468087 ↗ “atazanavir [ATV]” NCT00665847 ↗ “Atazanavir (ATV)” NCT02386098 ↗ “atazanavir (ATV)” NCT03631732 ↗ |
| Known as | ATZ | “Step 2 is open label. Regimens include 2 or 3 nucleoside reverse transcriptase inhibitors (NRTIs) in combination with EFV, atazanavir (ATZ), ritonavir-boosted ATZ, or tenofovir...” NCT00013520 ↗3“between danoprevir (DNV) when coadministered with low-dose ritonavir (r) and tenofovir disoproxil fumarate (TDF) or atazanavir (ATZ) in healthy volunteers” NCT01592305 ↗ “A drug-drug interaction between the anti-HIV drugs tenofovir DF (TDF) and atazanavir (ATZ) results in lower ATZ plasma levels” NCT01351740 ↗ “Atazanavir(ATZ) and Tenofovir(TDF)” NCT01368783 ↗ |
| Known as | BMS-232632 | “Novel Protease Inhibitor (BMS 232632, Atazanavir, ATV, Reyataz) in Combination Regimens” NCT00006604 ↗1“Atazanavir (BMS-232632)” NCT00046345 ↗ |
| Known as | BMS-232632-05 | ChEMBL registry synonym — accepted as the source's own label CHEMBL1163 ↗ |
| Known as | CGP-73547 | ChEMBL registry synonym — accepted as the source's own label CHEMBL1163 ↗ |
| Known as | NSC-742546 | ChEMBL registry synonym — accepted as the source's own label CHEMBL1163 ↗ |
| Known as | Reyataz | “Atazanavir (Reyataz) was the first protease inhibitor once daily approved in 2003 for the treatment of HIV patients.” NCT02473328 ↗9“Novel Protease Inhibitor (BMS 232632, Atazanavir, ATV, Reyataz) in Combination Regimens” NCT00006604 ↗ “Lamivudine (Epivir, GSK), Atazanavir (Reyataz, BMS), Ritonavir (Norvir, Abbott)” NCT01599364 ↗ “Atazanavir (Reyataz): capsules 150 mg (2 capsules/24h)” NCT00355719 ↗ “atazanavir (ATV; Reyataz®) + ritonavir (RTV; Norvir®)” NCT02616783 ↗ “atazanavir (ATV; Reyataz®) + ritonavir (RTV; Norvir®)” NCT02605954 ↗ “Drug: Atazanavir (Reyataz)” NCT00885482 ↗ “atazanavir (Reyataz)” NCT00426296 ↗ |
| Known as | Reyataz (atazanavir) | “Reyataz (atazanavir)” NCT01902186 ↗ |
| Action | Inhibit | “the protease inhibitor (PI) atazanavir (ATV)” NCT00006604 ↗ |
| Modality | Other / unclassified | “ritonavir-boosted (RTV) protease inhibitor regimen of atazanavir (ATV)/RTV+FTC/TDF” PMID 22748590 ↗ Jun 2012 |
| Route | Oral | “Active Comparator, Capsules, tablets, Oral” NCT00035932 ↗ |
| Target | UGT1A1 | “uridine diphosphate-glucuronosyl transferase 1A1 (UGT1A1) enzyme pathway.(5).ATV is a known inhibitor of this enzyme pathway” NCT00814879 ↗ |