Drugs / Zidovudine
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Zidovudine

Small molecule

Developed for
HIV infectious disease · AIDS · Kaposi's sarcoma · lipodystrophy · lymphoma · AIDS dementia complex · tuberculosis · non-Hodgkin lymphoma
+19 more · adult T-cell leukemia/lymphoma · Aicardi-Goutieres syndrome · AIDS related complex · brain disorder · cytomegalovirus retinitis · Epstein-Barr virus-associated lymphoproliferative disorder · hepatitis B virus infection · KSHV inflammatory cytokine syndrome · lymphoproliferative syndrome · multicentric Castleman disease · neuromuscular disease · peripheral T-cell lymphoma, not otherwise specified · post-transplant lymphoproliferative disease · primary biliary cholangitis · progressive multifocal leukoencephalopathy · psoriasis · tropical spastic paraparesis · central nervous system disorder · dementia
Investigated by
National Institute of Allergy and Infectious Diseases (NIAID) · Glaxo Wellcome · Bristol-Myers Squibb · Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) · Hoffmann-La Roche · Gilead Sciences
+115 more · Merck Sharp & Dohme LLC · National Cancer Institute (NCI) · Abbott · Boehringer Ingelheim · GlaxoSmithKline · Harvard School of Public Health (HSPH) · Pharmacia and Upjohn · University of Miami · ANRS, Emerging Infectious Diseases · French National Agency for Research on AIDS and Viral Hepatitis · G D Searle · International Maternal Pediatric Adolescent AIDS Clinical Trials Group · Kirby Institute · Makerere University · Research Institute for Development · Upjohn · ViiV Healthcare · AIDS Malignancy Consortium · Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections · Amgen · Genentech, Inc. · International Antiviral Therapy Evaluation Center · National Center for AIDS/STD Control and Prevention, China CDC · National Heart, Lung, and Blood Institute (NHLBI) · Sandoz · St Vincent's Hospital, Sydney · University of California, San Diego · AIDS Project Los Angeles · Amsterdam UMC, location VUmc · Assistance Publique - Hôpitaux de Paris · Axcan Pharma · Beijing YouAn Hospital · Biogen · Botswana Harvard Health Partnership · Botswana Ministry of Health · Brigham and Women's Hospital · CIHR Canadian HIV Trials Network · Centers for Disease Control and Prevention · Centre Hospitalier Universitaire Saint Pierre · Centre de Sante de Ziguinchor, Casamance, Senegal · Centro di Riferimento Oncologico - Aviano · China Medical University, China · Chiron Corporation · Chulalongkorn University · Clinique des Maladies Infectieuses, CHNU de Fann, Dakar, Senegal · Department for International Development, United Kingdom · Doris Duke Charitable Foundation · Duke University · Dupont Merck · Fight AIDS and Infectious Diseases Foundation · First Affiliated Hospital of Guangxi Medical University · Fundacion SEIMC-GESIDA · Garvan Institute of Medical Research · Genelabs Technologies · Germans Trias i Pujol Hospital · Guangdong Provincial Maternal and Child Health Hospital · HIV Prevention Trials Network · Hoechst Marion Roussel · Infectious Diseases Institute, Uganda · Initiative Senegalaise d'Acces aux Antiretroviraux (ISAARV) · Institut de Médecine et d'Epidémiologie Appliquée - Fondation Internationale Léon M'Ba · Janssen Pharmaceutica · Janssen Research & Development, LLC · Janssen-Cilag GmbH · Johann Wolfgang Goethe University Hospital · Kibongoto National Tuberculosis Hospital, Tanzania · Kilimanjaro Christian Medical Centre, Tanzania · Los Angeles County Department of Public Health · Los Angeles LGBT Center · Maternal and Child Health Hospital of Guangxi Province · Maternal and Child Health Hospital of Sichuan Province · Maternal and Child Health Hospital of Xinjiang Uygur Autonomous Region · Maternal and Child Health Hospital of Yunan Province · Mbarara University of Science and Technology · all 121 on the full record

Regulatory milestones approvals, filings & regulatory actions · 9 recorded

MilestoneJurisdictionBrandIndicationDateSentence it was read from
Label expansions (7) US (FDA) RETROVIR — 1990-01-12 – 2009-11-06 fda.gov ↗
Approved EU (EMA) Combivir — 1998-03-18 europa.eu ↗
Approved US (FDA) RETROVIR — 1987-03-19 fda.gov ↗

Trials 274 · started per year

today
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EU approved 1998
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PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 01 trial
Phase 0 NCT02655471 Jul 2017 → Mar 2019 tropical spastic paraparesis Universidad Peruana Cayetano Heredia Completed No outcome recorded
Phase 151 trials · 1 missed
Phase 1 NCT00470041 Jun 2007 → Oct 2009 — University Ghent Completed No outcome recorded
Phase 1 NCT02249416 Nov 2001 → Feb 2002 — Boehringer Ingelheim Completed No outcome recorded
Phase 1 NCT00001644 Mar 1997 → Feb 2010 HIV infectious disease National Institute of Allergy and Infectious Diseases (NIAID) Completed No outcome recorded
Phase 1 NCT00000696 ? → Nov 1993 HIV infectious disease National Institute of Allergy and Infectious Diseases (NIAID) Completed No outcome recorded
Phase 1 NCT00000661 — HIV infectious disease National Institute of Allergy and Infectious Diseases (NIAID) Completed No outcome recorded
Phase 1 NCT00000986 ? → Jan 1994 HIV infectious disease National Institute of Allergy and Infectious Diseases (NIAID) Completed No outcome recorded
Phase 1 NCT00000755 ? → Mar 1993 HIV infectious disease National Institute of Allergy and Infectious Diseases (NIAID) Completed No outcome recorded
Phase 1 NCT00000701 ? → Feb 1990 HIV infectious disease National Institute of Allergy and Infectious Diseases (NIAID) Completed No outcome recorded
Phase 1 NCT00001002 ? → Jun 1991 HIV infectious disease National Institute of Allergy and Infectious Diseases (NIAID) Completed No outcome recorded
Phase 1 NCT00001010 ? → Oct 1990 HIV infectious disease National Institute of Allergy and Infectious Diseases (NIAID) Completed No outcome recorded
Phase 1/22 trials
Phase 1/2 NCT00672412 Oct 2008 → Jan 2010 HIV infectious disease National Institute of Allergy and Infectious Diseases (NIAID) Completed No outcome recorded
Phase 1/2 NCT00432016 Feb → May 2007 HIV infectious disease RFS Pharma, LLC Completed No outcome recorded
Phase 270 trials · 2 met primary · 2 missed
Phase 2 NCT03922724 Apr 2019 → Jun 2027 expected lymphoproliferative syndrome, peripheral T-cell lymphoma, not otherwise specified National Cancer Institute (NCI) Active not recruiting No outcome recorded
Phase 2 NCT03602690 Oct 2018 → Apr 2022 HIV infectious disease ANRS, Emerging Infectious Diseases Unknown No outcome recorded
Phase 2 NCT02737046 Dec 2016 → Dec 2024 adult T-cell leukemia/lymphoma University of Miami Completed No outcome recorded
Phase 2 NCT02363452 Sep 2015 → Jan 2018 Aicardi-Goutieres syndrome Assistance Publique - Hôpitaux de Paris Completed No outcome recorded
Phase 2 NCT01441063 Sep 2011 → Jun 2018 multicentric Castleman disease National Cancer Institute (NCI) Completed No outcome recorded
Phase 2 NCT01419561 Sep 2011 → Dec 2028 expected KSHV inflammatory cytokine syndrome, human herpesvirus 8 infection National Cancer Institute (NCI) Recruiting No outcome recorded
Phase 2 NCT00949234 Mar → Jun 2010 HIV infectious disease University of California, Los Angeles Completed No outcome recorded
Phase 2 NCT01964755 Apr 2009 → Jun 2018 Epstein-Barr virus-associated lymphoproliferative disorder, post-transplant lymphoproliferative disease University of Miami Terminated No outcome recorded
Phase 2 NCT00109590 Jun 2006 → Oct 2008 HIV infectious disease National Institute of Allergy and Infectious Diseases (NIAID) Completed No outcome recorded
Phase 2 NCT00270296 Jun 2006 → Mar 2009 HIV infectious disease National Institute of Allergy and Infectious Diseases (NIAID) Completed No outcome recorded
Phase 2/35 trials · 2 missed
Phase 2/3 NCT02150993 Jan 2016 → May 2019 — ANRS, Emerging Infectious Diseases Completed No outcome recorded
Phase 2/3 NCT02369406 May 2015 → Nov 2020 overdue AIDS Harvard School of Public Health (HSPH) Active not recruiting No outcome recorded
Phase 2/3 NCT00624195 Mar 2007 → Feb 2012 HIV infectious disease University of California, San Diego Completed Missed primary
Phase 2/3 NCT00490620 Jan 2004 → Apr 2007 primary biliary cholangitis University of Alberta Completed No outcome recorded
Phase 2/3 NCT00039741 Aug 2002 → Aug 2009 HIV infectious disease National Institute of Allergy and Infectious Diseases (NIAID) Completed Missed primary
Phase 341 trials · 6 met primary · 4 missed
Phase 3 NCT03988452 Jul 2019 → Sep 2020 HIV infectious disease Makerere University Unknown Met primary
Phase 3 NCT02231281 Aug 2014 → Aug 2018 — Yongtao Sun, MD, PhD Unknown No outcome recorded
Phase 3 NCT01352715 Mar 2012 → Oct 2014 HIV infectious disease Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections Completed Met primary
Phase 3 NCT01511237 Dec 2011 → Jun 2015 HIV infectious disease Research Institute for Development Completed No outcome recorded
Phase 3 NCT01516970 Nov 2011 → Aug 2013 HIV infectious disease Janssen-Cilag GmbH Completed Missed primary
Phase 3 NCT01440569 Sep 2011 → Aug 2012 AIDS Gilead Sciences Completed No outcome recorded
Phase 3 NCT00573001 Jul 2008 → Jul 2011 HIV infectious disease French National Agency for Research on AIDS and Viral Hepatitis Completed No outcome recorded
Phase 3 NCT00102960 Jul 2005 → Sep 2012 HIV infectious disease National Institute of Allergy and Infectious Diseases (NIAID) Completed Met primary
Phase 3 NCT00074581 Feb 2005 → May 2015 HIV infectious disease National Institute of Allergy and Infectious Diseases (NIAID) Completed Met primary
Phase 3 NCT00323544 Oct 2004 → Jun 2007 HIV infectious disease Gilead Sciences Completed No outcome recorded
Phase 435 trials · 3 met primary · 2 missed
Phase 4 NCT06337032 Aug 2024 → Mar 2034 expected HIV infectious disease Gilead Sciences Recruiting No outcome recorded
Phase 4 NCT03642704 Feb 2017 → Sep 2019 — ANRS, Emerging Infectious Diseases Completed No outcome recorded
Phase 4 NCT02712801 Apr 2016 → Dec 2021 HIV infectious disease National Center for Women and Children's Health, China CDC Completed No outcome recorded
Phase 4 NCT01275625 Jun 2011 → Oct 2012 HIV infectious disease ViiV Healthcare Completed No outcome recorded
Phase 4 NCT01075152 Nov 2010 → Oct 2012 AIDS, Cryptococcal meningitis University of Minnesota Completed Missed primary
Phase 4 NCT00955968 Jan 2010 → Aug 2016 HIV infectious disease International Maternal Pediatric Adolescent AIDS Clinical Trials Group Completed No outcome recorded
Phase 4 NCT00753324 May 2009 → Jan 2012 HIV infectious disease University of North Carolina, Chapel Hill Completed Met primary
Phase 4 NCT01088516 Dec 2008 → Nov 2011 HIV infectious disease University of Zambia Completed No outcome recorded
Phase 4 NCT00865475 Dec 2008 → Mar 2013 HIV infectious disease Fundacion SEIMC-GESIDA Completed No outcome recorded
Phase 4 NCT01772940 Dec 2008 → Oct 2011 HIV infectious disease Centre Hospitalier Universitaire Saint Pierre Completed Missed primary
Phase not applicable69 trials · 1 met primary
— NCT03394196 Jul 2018 → May 2020 — University of Washington Terminated No outcome recorded Stop: Business
— NCT01344148 Feb 2009 → Jun 2011 AIDS Shanghai Public Health Clinical Center Unknown No outcome recorded
— NCT00872872 May 2008 → Apr 2019 — Thai Red Cross AIDS Research Centre Completed No outcome recorded
— NCT00120510 Jul 2007 → Sep 2009 HIV infectious disease, tuberculosis National Institute of Allergy and Infectious Diseases (NIAID) Completed Met primary
— NCT00100568 Jul 2006 → Jun 2009 HIV infectious disease National Institute of Allergy and Infectious Diseases (NIAID) Completed No outcome recorded
— NCT00100594 May 2005 → May 2007 HIV infectious disease National Institute of Allergy and Infectious Diseases (NIAID) Completed No outcome recorded
— NCT00080522 Feb 2005 → Jan 2007 HIV infectious disease National Institute of Allergy and Infectious Diseases (NIAID) Completed No outcome recorded
— NCT00001119 Oct 1999 → Jun 2004 HIV infectious disease National Institute of Allergy and Infectious Diseases (NIAID) Completed No outcome recorded
— NCT00002411 Mar 1998 → Sep 1999 HIV infectious disease Bristol-Myers Squibb Completed No outcome recorded
— NCT00000897 ? → Oct 2005 HIV infectious disease National Institute of Allergy and Infectious Diseases (NIAID) Completed No outcome recorded
Comparator or background therapy133 trials
Phase 0 NCT00719602 Comparator Aug 2009 → Aug 2013 HIV infectious disease, malaria International Maternal Pediatric Adolescent AIDS Clinical Trials Group Completed No outcome recorded
Phase 1 NCT02832778 Background Nov 2016 → Jan 2018 HIV infectious disease St Stephens Aids Trust Unknown No outcome recorded
Phase 1 NCT02499874 Background Aug 2015 → Oct 2017 HIV infectious disease St Stephens Aids Trust Completed No outcome recorded
Phase 1 NCT00326716 Background Jun 2006 → Jan 2009 HIV infectious disease Bristol-Myers Squibb Completed No outcome recorded
Phase 1 NCT00032669 Background Mar 2002 → Apr 2006 HIV infectious disease National Cancer Institute (NCI) Completed No outcome recorded
Show all 133 trials opens the full record — a long page

News releases announcing trial results or a regulatory action · 10

DateIssuerRelease
2007-10-29 Gilead Sciences Results Gilead Announces 48-Week Data Evaluating Switching from Combivir(R) To Truvada(R) Among Virologically-Suppressed HIV Patients gilead.com ↗
In the SWEET (Simplification With Easier Emtricitabine and Tenofovir) study, patients who switched from Combivir to Truvada, both in combination with once-daily Sustiva(R) (efavirenz), experienced improvements in a number of treatment-related side effects.
2007-07-23 Gilead Sciences Results 144-Week Data from Gilead's Study 934 Comparing Truvada(R) to Combivir(R) Both in Combination with Sustiva(R) Presented At International AIDS Society Meeting in Sydney gilead.com ↗
Gilead Sciences, Inc. (Nasdaq:GILD) today announced the presentation of 144-week data from an ongoing clinical trial, Study 934, comparing a once-daily regimen of Truvada(R) (emtricitabine and tenofovir disoproxil fumarate) and Sustiva(R) (efavirenz) to a twice-daily regimen of Combivir(R) (lamivudine/zidovudine) with Sustiva once daily in treatment-naive adults with HIV.
2006-12-15 Gilead Sciences Results 96-Week Data From Gilead's Study 934 Comparing Viread(R) and Emtriva(R) to Combivir(R) Both in Combination With Sustiva(R) Published in Journal of Acquired Immune Deficiency Syndrome gilead.com ↗
Gilead Sciences, Inc. (Nasdaq:GILD) today announced the publication of 96-week data from an ongoing clinical trial, Study 934, in the Journal of Acquired Immune Deficiency Syndrome (JAIDS).
2006-08-14 Gilead Sciences Results 96-Week Data from Gilead's Study 934 Comparing Viread(R) and Emtriva(R) to Combivir(R) Both in Combination with Sustiva(R) Presented at XVI International AIDS Conference gilead.com ↗
Ninety-six week data are being presented by Joel Gallant, MD, Johns Hopkins University School of Medicine, Baltimore, at the XVI International AIDS Conference taking place August 13-18 in Toronto (Poster # TUPE0064).
2006-01-18 Gilead Sciences Results Data Comparing Viread(R) and Emtriva(R) to Combivir(R) as Part of Combination HIV Therapy Published in New England Journal of Medicine gilead.com ↗
Publication Describes Superior Viral Suppression with Fewer Adverse Events Leading to Discontinuation for Patients Taking Viread and Emtriva at 48 Weeks
2005-02-03 Gilead Sciences Results Gilead Announces Preliminary 48-Week Data From Study 934 Comparing Viread and Emtriva to Combivir Both in Combination With Sustiva in Patients With HIV gilead.com ↗
Gilead Sciences (Nasdaq:GILD) today announced preliminary 48-week data from the company's Study 934.
2004-10-31 Gilead Sciences Results Interim 24-Week Data from Study 934 Comparing a Regimen of Viread and Emtriva Versus Combivir, Both in Combination with Efavirenz, in Patients with HIV Presented at 44th ICAAC gilead.com ↗
Although both triple-drug regimens are relatively convenient, we observed a difference in the two arms, with more patients discontinuing in the Combivir group due to adverse events.
2004-08-26 Gilead Sciences Results Gilead Announces Preliminary 24-Week Data from Study 934 Comparing Viread and Emtriva to Combivir Both in Combination With Efavirenz In Patients With HIV gilead.com ↗
Preliminary results show a statistically significant difference favoring Viread/Emtriva in the percentage of patients who achieved and maintained HIV RNA less than 400 copies/mL at 24 weeks, based on the FDA Time to Loss of Virologic Response algorithm (TLOVR).
2001-06-05 Gilead Sciences Results Gilead Sciences Presents Data Characterizing Resistance Profile of Tenofovir DF, Investigational Agent for the Treatment of HIV gilead.com ↗
The results demonstrate that chain-terminator removal occurs more readily with nucleosides than nucleotides and may contribute to the higher-level of resistance associated with nucleosides.
1998-09-23 Gilead Sciences Results Gilead Sciences Provides Update on PREVEON® Clinical Program for the Treatment of HIV gilead.com ↗
These data demonstrate that PREVEON has durable anti-HIV activity in treatment-experienced patients, including those infected with strains of HIV resistant to most currently approved therapies.

All press releases naming this drug 10 releases

DateIssuerRelease

Evidence & citations 12 cited values

Every value below carries the sentence it was read from. 417 sources stand behind the page.

FieldValueCited text
Known as Zidovudine “Generic names: Efavirenz/Emtricitabine/Tenofovir, Lamivudine/Zidovudine, Emtricitabine, Lamivudine, Abacavir/Lamivudine, Zidovudine, Abacavir/Lamivudine/Zidovudine,...” NCT00624195 ↗
408

“It may include one or two nucleoside reverse transcriptase inhibitors, such as zidovudine, didanosine, lamuvidine, zalcitabine, stavudine), a non- nucleoside reverse...” NCT00032669 ↗

“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 will receive 2 investigator-selected NRTIs, which may include abacavir (ABC), lamivudine (3TC)/zidovudine (ZDV), didanosine (DDI), emtricitabine (FTC), ABC/3TC,...” NCT01363011 ↗

“NRTIs included abacavir, emtricitabine, Combivir (lamivudine/zidovudine, coformulated), Epzicom (abacavir/lamivudine, coformulated), lamivudine, stavudine, tenofovir DF,...” NCT01252940 ↗

“Investigator selected 2 NRTIs: (1) Zidovudine and lamivudine (Combivir) and (2) tenofovir disoproxil fumarate and emtricitabine (Truvada) will be administered as per the...” NCT00110305 ↗

“These study will explore how fast NVP is eliminated from women after delivery and to see if given zidovudine/lamivudine (AZT/3TC) for 1 or 2 weeks after NVP discontinuation can...” NCT00872872 ↗

“Children initiated ART using an induction-maintenance approach, starting with open-label four-drug lamivudine, abacavir, NNRTI, plus zidovudine for 36 weeks, then open-label...” NCT02028676 ↗

“For those subjects in South Africa and Argentina who were previously receiving Combivir along with maraviroc in Study A4001026, Combivir will be supplied as tablets containing...” NCT01776996 ↗

“Participants who will be enrolled in this trial would keep their previous combined antiretroviral therapy, such as zidovudine or stavudine plus lamivudine plus nevirapine or efavirenz.” NCT02002286 ↗

“NRTIs may include emtricitabine (FTC)/tenofovir disoproxil fumarate (TDF), zidovudine+FTC/TDF, abacavir (ABC)+TDF, ABC+FTC/TDF, ABC+lamivudine (3TC), or didanosine (DDI)+FTC.” NCT01440569 ↗

Show 398 more sources

Known as 3'-Azido-3'-Deoxythymidine “Phase I Trial of the Combination of 3'-Azido-3'-Deoxythymidine (Zidovudine) and Recombinant Interleukin-2” NCT00001005 ↗
Known as Azidothymidine “The purpose of this study is to see if giving azidothymidine (AZT) to HIV-positive patients with hemophilia is safe and if it is effective in lowering HIV levels and boosting...” NCT00000705 ↗
2

“A Clinical Study Examining the Pharmacokinetics and Bioavailability of Azidothymidine (AZT, Zidovudine) in Patients With Human Immunodeficiency Virus (HIV) Infection and Hepatic Disease” NCT00001001 ↗

“Study of Bleeding Tendency, Platelet Function, and Pharmacokinetics of Azidothymidine (AZT) and Motrin (Ibuprofen) in HIV-Infected Hemophiliacs” NCT00002276 ↗

Known as AZT “To evaluate the effect of anti-HIV immune serum globulin (HIVIG) versus immune globulin (IVIG) administered during pregnancy and to the newborn, in combination with zidovudine...” NCT00000751 ↗
171

“To determine if alternating zidovudine (AZT) and zalcitabine (dideoxycytidine; ddC) (first one and then the other) or intermittent therapy (1 week of drug then 1 week off) will...” NCT00000718 ↗

“The purpose of this study is to determine the short term safety, tolerance, and antiviral effect of zidovudine (AZT) and amdoxovir (AMDX, DAPD) in combination, and whether the...” NCT00432016 ↗

“To compare the effectiveness of zalcitabine ( dideoxycytidine; ddC ) therapy to zidovudine ( AZT ) in the treatment of AIDS or advanced AIDS related complex ( ARC ) in patients...” NCT00000678 ↗

“The investigators propose to evaluate the safety of combination therapy comprising the three nucleoside analog reverse-transcriptase inhibitors (NRTIs) zidovudine (AZT),...” NCT02363452 ↗

“To compare the efficacy of lamivudine (3TC) and zidovudine (AZT) in combination versus the better of didanosine (ddI) monotherapy or ddI/AZT combination, in symptomatic HIV-1...” NCT00001066 ↗

“To determine if the pharmacokinetics of low doses of zidovudine (AZT) (that is, how fast AZT reaches the blood, what concentration of AZT is attained in the blood, and how long...” NCT00000732 ↗

“Preliminary studies using human liver tissue have shown that valproic acid inhibits the metabolic inactivation of zidovudine (AZT), which may prolong the plasma half-life of...” NCT00000629 ↗

“To determine the effects of zidovudine (AZT) alone and in combination with didanosine (ddI) on viral load in the lymphoid tissue and blood of antiretroviral-naive, HIV-infected...” NCT00001057 ↗

“To evaluate the anti-HIV effect of single agent versus combination therapy with zidovudine (AZT) and interferon alfa-2a (IFN-A2a), as measured by p24 protein expression, viral...” NCT00000696 ↗

“Primary: To compare the efficacy of zidovudine ( AZT ) given alone versus AZT plus didanosine ( ddI ) versus AZT plus zalcitabine ( dideoxycytidine; ddC ) in delaying the...” NCT00001022 ↗

Show 161 more sources

Known as Retrovir “100 patients will be randomized to receive Zerit (Stavudine) + Epivir (Lamivudine) + Crixivan (Indinavir) and 100 patients will be randomized to receive Retrovir (Zidovudine) +...” NCT00002369 ↗
8

“A Multi-Center, Double-Blind Trial to Evaluate the Safety and Efficacy of Concurrent Retrovir (Zidovudine) and Zovirax (Acyclovir) Therapy in Patients With Early Symptomatic...” NCT00002290 ↗

“To evaluate the safety and effectiveness of Retrovir (AZT) when used as prophylaxis for health care workers at risk for HIV infection from exposure to HIV-contaminated blood or...” NCT00002287 ↗

“A Pilot Study To Evaluate the Effect of Retrovir (Zidovudine: AZT) in the Treatment of Human Immunodeficiency Virus (HIV) Associated Dementia and Neuromuscular Diseases” NCT00002044 ↗

“To evaluate the feasibility of Retrovir (AZT) in the treatment of psoriasis in HIV antibody positive patients.” NCT00002286 ↗

“chronic administration of Retrovir (AZT) to adult patients with early manifestations of HIV disease.” NCT00002045 ↗

“300 mg zidovudine (Retrovir tablets, GlaxoSmithKline)” NCT00966160 ↗

“Retrovir Brand Zidovudine (AZT) Therapy” NCT00000662 ↗

“Retrovir (Zidovudine)” NCT00002168 ↗

Known as Retrovir(R) “Zidovudine, or Retrovir(R), is used at a high dose.” NCT00092222 ↗
Known as ZCV “Zidovudine (ZCV)” NCT00144183 ↗
Known as ZDV “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 ↗
67

“Participants will receive 2 investigator-selected NRTIs, which may include abacavir (ABC), lamivudine (3TC)/zidovudine (ZDV), didanosine (DDI), emtricitabine (FTC), ABC/3TC,...” NCT01363011 ↗

“The purpose of this study is to see if it is safe to give saquinavir-SGC (SQV) combined with low-dose ritonavir (RTV) plus zidovudine (ZDV) and lamivudine (3TC) to HIV-positive...” NCT00000920 ↗

“A Double-Blind, Randomized, Multicenter Trial to Evaluate the Safety and Efficacy of the Combination of 1592U89/Zidovudine (ZDV)/Lamivudine (3TC) Versus the Combination of...” NCT00002391 ↗

“The efficacy and tolerance of switching from zidovudine (ZDV) and lamivudine (3TC) in clinically stable HIV-infected children with incomplete viral suppression to stavudine...” PMID 11840078 ↗ Feb 2002

“Arm I options are enteric-coated didanosine (ddI-EC) plus lamivudine (3TC), ddI-EC plus zidovudine (ZDV), ZDV plus 3TC (or Combivir), stavudine (d4T) plus 3TC, or ddI-EC plus...” NCT00014937 ↗

“Double reverse transcriptase inhibitor (RTI) therapy consisting of any two therapy combinations of: didanosine (ddI), lamivudine (3TC), stavudine (d4T) or zidovudine (ZDV),...” NCT00002376 ↗

“The purpose of this study is to compare the safety and effectiveness of taking lamivudine (3TC) plus zidovudine (ZDV) plus a protease inhibitor (PI) with taking the 3TC/ZDV...” NCT00002203 ↗

“The purpose of this study is to see if it is safe and effective to give ritonavir (RTV) plus lamivudine (3TC) plus zidovudine (ZDV) to HIV-infected pregnant women during...” NCT00000888 ↗

“Treatment-naive adults were randomized to nevirapine (NVP) or ritonavir-boosted lopinavir (LPV/r) regimens each in combination with tenofovir (TDF)/emtricitabine (FTC) or...” PMID 25028911 ↗ May 2014

“The extent and manner by which HIV nucleoside reverse transcriptase inhibitors contribute to insulin resistance is unclear. We evaluated the effect of zidovudine/lamivudine...” PMID 19898246 ↗ Feb 2010

Show 57 more sources

Known as ZDV: zidovudine, azidothymidine, Retrovir “ZDV: zidovudine, azidothymidine, Retrovir” NCT02028676 ↗
Action Inhibit “previous studies have shown AZT to be an effective inhibitor of HIV reverse transcriptase” NCT00000695 ↗
Modality Small molecule “nucleoside analog” NCT00000781 ↗
Route Oral “AZT orally every 8 hours on days 1 through 4” NCT00000629 ↗