Meltdose Tacrolimus Pharmacokinetics
Abstract Background Nonadherence to immunosuppressive therapy contributes to the loss of grafts. One of the problem is the fractioning of immunosuppressive dose. In fact, it was demonstrated that a single daily dose (QD) is associated with an increased adherence to therapy compared with twice daily...
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description | Abstract Background Nonadherence to immunosuppressive therapy contributes to the loss of grafts. One of the problem is the fractioning of immunosuppressive dose. In fact, it was demonstrated that a single daily dose (QD) is associated with an increased adherence to therapy compared with twice daily dosing (BID). Tacrolimus (TAC), calcineurin inhibitor, is one of immunosuppression pillar in organ transplantation and its action is strongly correlated with blood concentration and therefore the therapeutic drug monitoring is recommended in the guidelines. However, one of the critical points of TAC is the poor and variable bioavailability that influences immunosuppression, and is also responsible for adverse effects. Methods MeltDose® Technology is a new technology to improve efficacy and/or reduce side effects. This new technology applied to TAC (Envarsus® or LCP-TAC) has achieved 4 main objectives: (1) improved bioavailability, (2) reduced dose fractioning to one tablet per day, (3) limited variability concentrations of TAC, and (4) lower doses of TAC will be administered. Results We analyzed the pharmacokinetic profile, efficacy, and security of Envarsus®. |
doi_str_mv | 10.1016/j.transproceed.2016.02.002 |
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One of the problem is the fractioning of immunosuppressive dose. In fact, it was demonstrated that a single daily dose (QD) is associated with an increased adherence to therapy compared with twice daily dosing (BID). Tacrolimus (TAC), calcineurin inhibitor, is one of immunosuppression pillar in organ transplantation and its action is strongly correlated with blood concentration and therefore the therapeutic drug monitoring is recommended in the guidelines. However, one of the critical points of TAC is the poor and variable bioavailability that influences immunosuppression, and is also responsible for adverse effects. Methods MeltDose® Technology is a new technology to improve efficacy and/or reduce side effects. This new technology applied to TAC (Envarsus® or LCP-TAC) has achieved 4 main objectives: (1) improved bioavailability, (2) reduced dose fractioning to one tablet per day, (3) limited variability concentrations of TAC, and (4) lower doses of TAC will be administered. Results We analyzed the pharmacokinetic profile, efficacy, and security of Envarsus®.</description><identifier>ISSN: 0041-1345</identifier><identifier>EISSN: 1873-2623</identifier><identifier>DOI: 10.1016/j.transproceed.2016.02.002</identifier><identifier>PMID: 27109969</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Biological Availability ; Delayed-Action Preparations ; Drug Administration Schedule ; Drug Monitoring ; Graft Rejection - prevention & control ; Humans ; Immunosuppressive Agents - administration & dosage ; Immunosuppressive Agents - pharmacokinetics ; Kidney Transplantation ; Liver Transplantation ; Surgery ; Tacrolimus - administration & dosage ; Tacrolimus - pharmacokinetics ; Time Factors</subject><ispartof>Transplantation proceedings, 2016-03, Vol.48 (2), p.420-423</ispartof><rights>Elsevier Inc.</rights><rights>2016 Elsevier Inc.</rights><rights>Copyright © 2016 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c435t-5d92f44e4b7f6c475f3870bf3b13fd7076c1866db44f62ef2e899eb6c1a079933</citedby><cites>FETCH-LOGICAL-c435t-5d92f44e4b7f6c475f3870bf3b13fd7076c1866db44f62ef2e899eb6c1a079933</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.transproceed.2016.02.002$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27109969$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baraldo, M</creatorcontrib><title>Meltdose Tacrolimus Pharmacokinetics</title><title>Transplantation proceedings</title><addtitle>Transplant Proc</addtitle><description>Abstract Background Nonadherence to immunosuppressive therapy contributes to the loss of grafts. One of the problem is the fractioning of immunosuppressive dose. In fact, it was demonstrated that a single daily dose (QD) is associated with an increased adherence to therapy compared with twice daily dosing (BID). Tacrolimus (TAC), calcineurin inhibitor, is one of immunosuppression pillar in organ transplantation and its action is strongly correlated with blood concentration and therefore the therapeutic drug monitoring is recommended in the guidelines. However, one of the critical points of TAC is the poor and variable bioavailability that influences immunosuppression, and is also responsible for adverse effects. Methods MeltDose® Technology is a new technology to improve efficacy and/or reduce side effects. This new technology applied to TAC (Envarsus® or LCP-TAC) has achieved 4 main objectives: (1) improved bioavailability, (2) reduced dose fractioning to one tablet per day, (3) limited variability concentrations of TAC, and (4) lower doses of TAC will be administered. Results We analyzed the pharmacokinetic profile, efficacy, and security of Envarsus®.</description><subject>Biological Availability</subject><subject>Delayed-Action Preparations</subject><subject>Drug Administration Schedule</subject><subject>Drug Monitoring</subject><subject>Graft Rejection - prevention & control</subject><subject>Humans</subject><subject>Immunosuppressive Agents - administration & dosage</subject><subject>Immunosuppressive Agents - pharmacokinetics</subject><subject>Kidney Transplantation</subject><subject>Liver Transplantation</subject><subject>Surgery</subject><subject>Tacrolimus - administration & dosage</subject><subject>Tacrolimus - pharmacokinetics</subject><subject>Time Factors</subject><issn>0041-1345</issn><issn>1873-2623</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkctKAzEUhoMotlZfQYq4cDNjbk1mXAhSr1BRsK5DJnOCaedSkxmhb29KLYgrVyHn_Of2_QidEZwSTMTlIu28bsLKtwagTGmMpZimGNM9NCSZZAkVlO2jIcacJITxyQAdhbDA8U85O0QDKgnOc5EP0fkzVF3ZBhjPtfFt5eo-jF8_tK-1aZeugc6ZcIwOrK4CnPy8I_R-fzefPiazl4en6c0sMZxNumRS5tRyDryQVhguJ5ZlEheWFYTZUmIpDMmEKAvOraBgKWR5DkWMaizznLERutj2jad99hA6VbtgoKp0A20fFJEZ54LE3aP0aiuNS4fgwaqVd7X2a0Ww2lBSC_WbktpQUpiqSCkWn_7M6Ys65nalOyxRcLsVQLz2y4FXwThoDJTOg-lU2br_zbn-08ZUrnFGV0tYQ1i0vW8iT0VUiAXqbePXxi4iolUZJ-wbTGeTXA</recordid><startdate>20160301</startdate><enddate>20160301</enddate><creator>Baraldo, M</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20160301</creationdate><title>Meltdose Tacrolimus Pharmacokinetics</title><author>Baraldo, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-5d92f44e4b7f6c475f3870bf3b13fd7076c1866db44f62ef2e899eb6c1a079933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Biological Availability</topic><topic>Delayed-Action Preparations</topic><topic>Drug Administration Schedule</topic><topic>Drug Monitoring</topic><topic>Graft Rejection - prevention & control</topic><topic>Humans</topic><topic>Immunosuppressive Agents - administration & dosage</topic><topic>Immunosuppressive Agents - pharmacokinetics</topic><topic>Kidney Transplantation</topic><topic>Liver Transplantation</topic><topic>Surgery</topic><topic>Tacrolimus - administration & dosage</topic><topic>Tacrolimus - pharmacokinetics</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baraldo, M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Transplantation proceedings</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baraldo, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Meltdose Tacrolimus Pharmacokinetics</atitle><jtitle>Transplantation proceedings</jtitle><addtitle>Transplant Proc</addtitle><date>2016-03-01</date><risdate>2016</risdate><volume>48</volume><issue>2</issue><spage>420</spage><epage>423</epage><pages>420-423</pages><issn>0041-1345</issn><eissn>1873-2623</eissn><abstract>Abstract Background Nonadherence to immunosuppressive therapy contributes to the loss of grafts. One of the problem is the fractioning of immunosuppressive dose. In fact, it was demonstrated that a single daily dose (QD) is associated with an increased adherence to therapy compared with twice daily dosing (BID). Tacrolimus (TAC), calcineurin inhibitor, is one of immunosuppression pillar in organ transplantation and its action is strongly correlated with blood concentration and therefore the therapeutic drug monitoring is recommended in the guidelines. However, one of the critical points of TAC is the poor and variable bioavailability that influences immunosuppression, and is also responsible for adverse effects. Methods MeltDose® Technology is a new technology to improve efficacy and/or reduce side effects. This new technology applied to TAC (Envarsus® or LCP-TAC) has achieved 4 main objectives: (1) improved bioavailability, (2) reduced dose fractioning to one tablet per day, (3) limited variability concentrations of TAC, and (4) lower doses of TAC will be administered. Results We analyzed the pharmacokinetic profile, efficacy, and security of Envarsus®.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>27109969</pmid><doi>10.1016/j.transproceed.2016.02.002</doi><tpages>4</tpages></addata></record> |
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subjects | Biological Availability Delayed-Action Preparations Drug Administration Schedule Drug Monitoring Graft Rejection - prevention & control Humans Immunosuppressive Agents - administration & dosage Immunosuppressive Agents - pharmacokinetics Kidney Transplantation Liver Transplantation Surgery Tacrolimus - administration & dosage Tacrolimus - pharmacokinetics Time Factors |
title | Meltdose Tacrolimus Pharmacokinetics |
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