{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,2]],"date-time":"2026-09-02T04:02:18Z","timestamp":1788321738364,"version":"build-2803163510"},"reference-count":28,"publisher":"Wiley","issue":"7","license":[{"start":{"date-parts":[[2017,3,17]],"date-time":"2017-03-17T00:00:00Z","timestamp":1489708800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"DOI":"10.13039\/100004325","name":"AstraZeneca","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100004325","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000062","name":"National Institute of Diabetes and Digestive and Kidney Diseases","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100000062","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Diabetes Obesity Metabolism"],"published-print":{"date-parts":[[2017,7]]},"abstract":"<jats:sec>\n                    <jats:title>Aims<\/jats:title>\n                    <jats:p>\n                      Glucagon\u2010like peptide\u20101 receptor agonists and dipeptidyl peptidase\u20104 inhibitors treat type 2 diabetes through incretin\u2010signaling pathways. This study compared the efficacy and safety of the glucagon\u2010like peptide\u20101 receptor agonist exenatide once\u2010weekly (\n                      <jats:styled-content style=\"fixed-case\">M<\/jats:styled-content>\n                      iglyol) suspension for autoinjection (\n                      <jats:styled-content style=\"fixed-case\">QWS\u2010AI<\/jats:styled-content>\n                      ) with the dipeptidyl peptidase\u20104 inhibitor sitagliptin or placebo.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Materials and methods<\/jats:title>\n                    <jats:p>\n                      In this open\u2010label, multicentre study of patients with type 2 diabetes who had suboptimal glycaemic control on metformin monotherapy, 365 patients were randomized to receive exenatide 2.0\u2009mg\n                      <jats:styled-content style=\"fixed-case\">QWS\u2010AI<\/jats:styled-content>\n                      , sitagliptin 100\u2009mg once daily or oral placebo (3:2:1 ratio). The primary endpoint was change in glycated hemoglobin (\n                      <jats:styled-content style=\"fixed-case\">HbA1c<\/jats:styled-content>\n                      ) from baseline to 28\u2009weeks.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      At 28\u2009weeks, exenatide\n                      <jats:styled-content style=\"fixed-case\">QWS\u2010AI<\/jats:styled-content>\n                      significantly reduced\n                      <jats:styled-content style=\"fixed-case\">HbA1c<\/jats:styled-content>\n                      from baseline compared to sitagliptin (\u22121.13% vs \u22120.75% [baseline values, 8.42% and 8.50%, respectively];\n                      <jats:italic>\n                        <jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>\n                      <\/jats:italic>\n                      \u2009=\u2009.02) and placebo (\u22120.40% [baseline value, 8.50%];\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.001). More exenatide\n                      <jats:styled-content style=\"fixed-case\">QWS\u2010AI<\/jats:styled-content>\n                      \u2010treated patients achieved\n                      <jats:styled-content style=\"fixed-case\">HbA1c<\/jats:styled-content>\n                      &lt;7.0% than did sitagliptin\u2010 or placebo\u2010treated patients (43.1% vs 32.0% and 24.6%; both\n                      <jats:italic>\n                        <jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>\n                      <\/jats:italic>\n                      \u2009&lt;\u2009.05). Exenatide\n                      <jats:styled-content style=\"fixed-case\">QWS\u2010AI<\/jats:styled-content>\n                      and sitagliptin reduced fasting plasma glucose from baseline to 28\u2009weeks (\u221221.3 and \u221211.3\u2009mg\/dL) vs placebo (+9.6\u2009mg\/dL), with no significant difference between the 2 active treatments. Body weight decreased with both active treatments (\u22121.12 and \u22121.19\u2009kg), but not with placebo (+0.15\u2009kg). No improvement in blood pressure was observed in any group. The most common adverse events with exenatide\n                      <jats:styled-content style=\"fixed-case\">QWS\u2010AI<\/jats:styled-content>\n                      were gastrointestinal events and injection\u2010site reactions.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      This study demonstrated that exenatide\n                      <jats:styled-content style=\"fixed-case\">QWS\u2010AI<\/jats:styled-content>\n                      reduced\n                      <jats:styled-content style=\"fixed-case\">HbA1c<\/jats:styled-content>\n                      more than sitagliptin or placebo and was well tolerated.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/dom.12908","type":"journal-article","created":{"date-parts":[[2017,2,16]],"date-time":"2017-02-16T04:26:04Z","timestamp":1487219164000},"page":"979-988","source":"Crossref","is-referenced-by-count":53,"title":["Efficacy and safety of autoinjected exenatide once\u2010weekly suspension versus sitagliptin or placebo with metformin in patients with type 2 diabetes:\n                    <scp>T<\/scp>\n                    he\n                    <scp>DURATION\u2010NEO<\/scp>\n                    \u20102 randomized clinical study"],"prefix":"10.1111","volume":"19","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-1856-5574","authenticated-orcid":false,"given":"Kishore M.","family":"Gadde","sequence":"first","affiliation":[{"name":"Pennington Biomedical Research Center Louisiana State University  Baton Rouge Louisiana"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Marion L.","family":"Vetter","sequence":"additional","affiliation":[{"name":"Bristol\u2010Myers Squibb  Princeton New Jersey"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nayyar","family":"Iqbal","sequence":"additional","affiliation":[{"name":"AstraZeneca  Gaithersburg Maryland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Elise","family":"Hardy","sequence":"additional","affiliation":[{"name":"AstraZeneca  Gaithersburg Maryland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Peter","family":"\u00d6hman","sequence":"additional","affiliation":[{"name":"AstraZeneca  Gaithersburg Maryland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"name":"on behalf of the DURATION\u2010NEO\u20102 study investigators","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2017,3,17]]},"reference":[{"key":"e_1_2_6_2_1","doi-asserted-by":"publisher","DOI":"10.2337\/dc14-2441"},{"key":"e_1_2_6_3_1","doi-asserted-by":"publisher","DOI":"10.1007\/s12325-014-0166-0"},{"key":"e_1_2_6_4_1","unstructured":"Byetta (exenatide) injection: US prescribing information. 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