Maraviroc
Other / unclassified targets CCR5 via inhibition
Regulatory milestones approvals, filings & regulatory actions · 7 recorded
| Milestone | Jurisdiction | Brand | Indication | Date | Sentence it was read from |
|---|---|---|---|---|---|
| Label expansions (5) | US (FDA) | SELZENTRY | — | 2008-11-25 – 2020-10-30 | fda.gov ↗ |
| Approved | EU (EMA) | Celsentri | — | 2007-09-18 | europa.eu ↗ |
| Approved | US (FDA) | SELZENTRY | — | 2007-08-06 | fda.gov ↗ |
Trials 117 · started per year
Also used as a comparator or background therapy in 27 trials
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 14 trials | ||||||
| Phase 1 | NCT03060447 Background | May 2017 → Feb 2020 | HIV infectious disease | Gilead Sciences | Completed | No outcome recorded |
| Phase 1 | NCT01749566 Comparator | Dec 2012 → May 2015 | HIV infectious disease | Emory University | Completed | No outcome recorded |
| Phase 1 | NCT01597895 Comparator | Jul → Aug 2012 | — | ViiV Healthcare | Completed | No outcome recorded |
| Phase 1 | NCT00771823 Comparator | May → Nov 2008 | HIV infectious disease | St Stephens Aids Trust | Completed | No outcome recorded |
| Phase 23 trials | ||||||
| Phase 2 | NCT07080567 Comparator | Jul 2025 → Dec 2027 expected | ischemic stroke | Emmanuel Carrera | Recruiting | No outcome recorded |
| Phase 2 | NCT04966429 Comparator | May 2021 → Apr 2024 | cognitive disorder | Tel-Aviv Sourasky Medical Center | Unknown | No outcome recorded |
| Phase 2 | NCT00764465 Comparator | Oct → Dec 2008 | — | Garden State Infectious Disease Associates, PA | Completed | No outcome recorded |
| Phase 2/32 trials | ||||||
| Phase 2/3 | NCT06974084 Comparator | Jul → Dec 2026 expected | long COVID-19 | HealthBio, Inc. | Not yet recruiting | No outcome recorded |
| Phase 2/3 | NCT00098722 Comparator | Dec 2004 → Apr 2007 | HIV infectious disease | ViiV Healthcare | Completed | No outcome recorded |
| Phase 38 trials | ||||||
| Phase 3 | NCT03631732 Comparator | Aug 2018 → Aug 2019 | 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 | NCT02302547 Comparator | Dec 2014 → Aug 2017 | HIV infectious disease | University Hospital, Tours | Completed | No outcome recorded |
| Phase 3 | NCT02121795 Background | May 2014 → Aug 2015 | HIV infectious disease | Gilead Sciences | Completed | No outcome recorded |
| Phase 3 | NCT01348308 Comparator | Sep 2011 → Mar 2016 | AIDS | ANRS, Emerging Infectious Diseases | Completed | No outcome recorded |
| Phase 3 | NCT00844519 Comparator | Jan 2010 → Dec 2012 | HIV infectious disease, cardiovascular disorder | University of California, San Francisco | Completed | No outcome recorded |
| Phase 3 | NCT00708162 Background | Jul 2008 → Dec 2010 | HIV infectious disease | Gilead Sciences | Completed | No outcome recorded |
| Phase 3 | NCT00440271 Background | Feb 2007 → Oct 2008 | HIV infectious disease | Boehringer Ingelheim | Terminated | No outcome recorded |
| Phase 410 trials | ||||||
| Phase 4 | NCT02881762 Comparator | Jun 2017 → Mar 2019 | HIV infectious disease, hepatitis C virus infection | University of Maryland, Baltimore | Completed | No outcome recorded |
| Phase 4 | NCT01637259 Comparator | Jun 2012 → Dec 2015 | HIV infectious disease, proteinuria | Kirby Institute | Completed | No outcome recorded |
| Phase 4 | NCT01389063 Comparator | Jan 2012 → Sep 2014 | — | S.F.L. van Lelyveld | Unknown | No outcome recorded |
| Phase 4 | NCT01384682 Comparator | Aug 2011 → Dec 2015 | HIV infectious disease | Kirby Institute | Completed | No outcome recorded |
| Phase 4 | NCT00981773 Comparator | Sep 2009 → Mar 2013 | HIV infectious disease | Imperial College London | Terminated | No outcome recorded |
| Phase 4 | NCT01049204 Comparator | Jul 2009 → Jun 2011 | HIV infectious disease | St Stephens Aids Trust | Terminated | No outcome recorded |
| Phase 4 | NCT00870363 Comparator | Apr 2009 → Apr 2013 | HIV infectious disease | University of California, Davis | Completed | No outcome recorded |
| Phase 4 | NCT00782301 Comparator | Mar 2009 → Feb 2010 | HIV infectious disease, chronic hepatitis C virus infection, hepatitis B virus infection | ViiV Healthcare | Withdrawn | No outcome recorded |
| Phase 4 | NCT00875368 Comparator | Feb 2009 → Dec 2011 | HIV infectious disease | S.F.L. van Lelyveld | Completed | No outcome recorded |
| Phase 4 | NCT00853840 Comparator | Apr → May 2008 | AIDS | ViiV Healthcare | Completed | No outcome recorded |
Press releases naming this drug 1 release
| Date | Issuer | Release |
|---|---|---|
| 2014-07-22 | Pfizer | ViiV Healthcare presents phase III data comparing once-daily maraviroc in combination with darunavir/ritonavir with emtricitabine/tenofovir plus darunavir/ritonavir in treatment-naïve adults with HIV-1 pfizer.com ↗ |
Evidence & citations 12 cited values
Every value below carries the sentence it was read from. 148 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | Maraviroc | “Generic names: Efavirenz/Emtricitabine/Tenofovir, Lamivudine/Zidovudine, Emtricitabine, Lamivudine, Abacavir/Lamivudine, Zidovudine, Abacavir/Lamivudine/Zidovudine,...” NCT00624195 ↗142“The three antiretroviral drugs have been chosen because they are the only ones that allow administration at higher doses without causing increased toxicity: dolutegravir 50...” NCT06640192 ↗ “This is an open-label protocol designed to provide continued access to maraviroc to only those subjects who have completed previous studies of maraviroc and continue to receive...” NCT01776996 ↗ “Current ART regimen plus raltegravir and maraviroc Raltegravir : 400 mg PO BID for 56 weeks Maraviroc : 150, 300 or 600 mg PO BID depending on concomitant ART treatment, for 56 weeks” NCT01019551 ↗ “The following agents are allowed as part of the ART regimen: nucleoside reverse transcriptase inhibitors, raltegravir, dolutegravir (DTG), rilpivirine, and maraviroc.” NCT03060447 ↗ “We randomly assigned for 48 weeks 22 patients to continue their current first line regimen of Truvada® plus Kaletra® or intensify it with Maraviroc and Raltegravir.” PMID 25320633 ↗ Oct 2014 “A triple combination IVR building on this platform and delivering TDF-FTC along with the antiretroviral (ARV) agent maraviroc (MVC) also is under development.” PMID 30265679 ↗ Sep 2018 “Maraviroc inhibits CCR5-tropic HIV-1 across different subtypes in vitro and has demonstrated efficacy in clinical trials.” PMID 34160290 ↗ Jan 2021 “efavirenz (EFV), rilpivirine (RPV), raltegravir (RAL), dolutegravir (DTG), maraviroc (MVC), or nevirapine (NVP)” NCT02469246 ↗ “Tenofovir+Emtricitabine+Third agent (Including a fusion inhibitor: enfuvirtide or a CCR5 antagonist :maraviroc” NCT02302547 ↗ “As of today, maraviroc is the only CCR5-antagonist approved for HIV treatment.” NCT01378910 ↗ “etravirine, LAM, maraviroc, tenofovir disoproxil fumarate (TDF)” NCT00708162 ↗ “6. Maraviroc 150 mg twice a day” NCT02588820 ↗ “maraviroc (MVC; Selzentry®)” NCT02121795 ↗ “maraviroc 150 mg once daily” NCT01367236 ↗ “maraviroc (MVC)” NCT03631732 ↗ “Maraviroc,” NCT00440271 ↗ |
| Known as | Celsentri | “Maraviroc brand name in the EC is Celsentri.” NCT00884858 ↗3“maraviroc (Celsentri®): 150 mg bid.” NCT01033760 ↗ “maraviroc (Selzentry, Celsentri)” NCT07668505 ↗ “Maraviroc (Celsentri)” NCT01348308 ↗ |
| Known as | Maraviroc = Celsentri | “Maraviroc = Celsentri” NCT01190293 ↗ |
| Known as | Maraviroc(Selzentry) | “Maraviroc (Selzentry)” NCT01068873 ↗1“Maraviroc(Selzentry)” NCT01204905 ↗ |
| Known as | MVC | “The primary objective was to assess the effect of MVC intensification on latently infected CD4(+) T cells in chronically HIV-1-infected patients receiving antiretroviral...” PMID 22174752 ↗ Dec 201116“A strategy to modulate activation and trafficking of leukocytes to the lungs is by blocking CCR5 by using maraviroc (MVC), which has shown capable of modulating conditions of...” NCT04475991 ↗ “A single arm, open-labeled trial was conducted to examine the effect of maraviroc (MVC) intensification on monocyte inflammation and neuropsychological (NP) performance in 15...” PMID 25227930 ↗ Sep 2014 “Maraviroc (MVC) is a member of a new class of antiretroviral compounds known as small molecule CCR5 antagonists that block R5 HIV entry into cluster of differentiation 4 (CD4) cells.” NCT01276236 ↗ “A triple combination IVR building on this platform and delivering TDF-FTC along with the antiretroviral (ARV) agent maraviroc (MVC) also is under development.” PMID 30265679 ↗ Sep 2018 “Maraviroc (MVC) is a CCR5 antagonist that prevents virus entry blocking the binding of R5-tropic HIV to the cell surface CCR5 co-receptor.” NCT01190293 ↗ “Maraviroc (MVC), a chemokine receptor 5 antagonist, is a potential alternative component of therapy in those with R5-tropic virus.” PMID 27048747 ↗ Apr 2016 “efavirenz (EFV), rilpivirine (RPV), raltegravir (RAL), dolutegravir (DTG), maraviroc (MVC), or nevirapine (NVP)” NCT02469246 ↗ “Use of Maraviroc (MVC) in Immunological Non-responder HIV-1-infected Patients.” NCT00884858 ↗ “Tablets: daily 300 mg oral maraviroc, Selzentry®,(MVC) for 8 consecutive days” NCT02346084 ↗ “Chemokine Receptor 5 (CCR5) Entry Inhibitor Maraviroc (MVC)” NCT00764465 ↗ “using the CCR5 receptor antagonist maraviroc (MVC)” NCT01749566 ↗ “Maraviroc (MVC) is a drug, very well tolerated” NCT04710199 ↗ “Maraviroc (MVC), a CCR5 antagonist” NCT04965662 ↗ “Drug: Maraviroc (MVC)” NCT06974084 ↗ “maraviroc (MVC)” NCT03631732 ↗ “Maraviroc (MVC)” NCT02519777 ↗ |
| Known as | Rel-maraviroc | ChEMBL registry synonym — accepted as the source's own label CHEMBL256907 ↗ |
| Known as | Selzentry | “Maraviroc (Selzentry) is a HIV medication that works by blocking the entry of HIV in cells including monocytes/macrophages that use a receptor called CCR5.” NCT00987948 ↗4“by the CCR5 antagonist drug maraviroc (Selzentry) administered to healthy volunteers” NCT01719627 ↗ “Tablets: daily 300 mg oral maraviroc, Selzentry®,(MVC) for 8 consecutive days” NCT02346084 ↗ “maraviroc (Selzentry, Celsentri)” NCT07668505 ↗ |
| Known as | UK-427,857 | “Maraviroc (UK-427,857) 300 mg once daily added to Zidovudine/Lamivudine (300 mg/150 mg twice daily).” NCT03178084 ↗6“Maraviroc (UK-427,857), a selective and reversible CCR5 co-receptor antagonist” NCT00098748 ↗ “Maraviroc (UK-427,857), a selective and reversible CCR5 coreceptor antagonist” NCT00098293 ↗ “Maraviroc (UK-427,857), a selective and reversible CCR5 coreceptor antagonist” NCT00098306 ↗ “Maraviroc (UK-427,857), a selective and reversible CCR5 coreceptor antagonist” NCT00098722 ↗ “Maraviroc (UK-427,857)” NCT00634959 ↗ “Maraviroc (UK-427,857)” NCT00643643 ↗ |
| Action | Inhibit | “a selective and reversible CCR5 coreceptor antagonist” NCT00098293 ↗ |
| Modality | Other / unclassified | “Maraviroc is a new ART agent from a novel class of HIV inhibitors, entry inhibitors” NCT00870363 ↗ |
| Route | Oral | “300 mg (2- 150 mg tablets) are administered by mouth twice a day (BID) for 12 weeks.” NCT00427934 ↗ |
| Target | CCR5 | “a selective and reversible CCR5 coreceptor antagonist” NCT00098306 ↗ |