<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chen CD</submitter><funding>NCATS NIH HHS</funding><funding>NIA NIH HHS</funding><funding>NINDS NIH HHS</funding><funding>NIH</funding><funding>NIH HHS</funding><pagination>2669-2682</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10330155</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>50(9)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Pittsburgh Compound-B (&lt;sup>11&lt;/sup>C-PiB) and &lt;sup>18&lt;/sup>F-florbetapir are amyloid-β (Aβ) positron emission tomography (PET) radiotracers that have been used as endpoints in Alzheimer's disease (AD) clinical trials to evaluate the efficacy of anti-Aβ monoclonal antibodies. However, comparing drug effects between and within trials may become complicated if different Aβ radiotracers were used. To study the consequences of using different Aβ radiotracers to measure Aβ clearance, we performed a head-to-head comparison of &lt;sup>11&lt;/sup>C-PiB and &lt;sup>18&lt;/sup>F-florbetapir in a Phase 2/3 clinical trial of anti-Aβ monoclonal antibodies.&lt;h4>Methods&lt;/h4>Sixty-six mutation-positive participants enrolled in the gantenerumab and placebo arms of the first Dominantly Inherited Alzheime</pubmed_abstract><journal>European journal of nuclear medicine and molecular imaging</journal><pubmed_title>Longitudinal head-to-head comparison of &amp;lt;sup&amp;gt;11&amp;lt;/sup&amp;gt;C-PiB and &amp;lt;sup&amp;gt;18&amp;lt;/sup&amp;gt;F-florbetapir PET in a Phase 2/3 clinical trial of anti-amyloid-β monoclonal antibodies in dominantly inherited Alzheimer's disease.</pubmed_title><pmcid>PMC10330155</pmcid><funding_grant_id>K01 AG080123</funding_grant_id><funding_grant_id>R01 AG052550</funding_grant_id><funding_grant_id>R01AG53267-S1</funding_grant_id><funding_grant_id>UF1 AG032438</funding_grant_id><funding_grant_id>T32 AG058518</funding_grant_id><funding_grant_id>RF1 AG073424</funding_grant_id><funding_grant_id>UL1 TR001863</funding_grant_id><funding_grant_id>P30 AG072980</funding_grant_id><funding_grant_id>U01AG042791</funding_grant_id><funding_grant_id>U01 AG042791</funding_grant_id><funding_grant_id>U19 AG032438</funding_grant_id><funding_grant_id>P30NS098577</funding_grant_id><funding_grant_id>U01AG042791-S1</funding_grant_id><funding_grant_id>R01AG052550-01A1</funding_grant_id><funding_grant_id>P30 AG066508</funding_grant_id><funding_grant_id>R01 AG053267</funding_grant_id><funding_grant_id>P30 AG066462</funding_grant_id><funding_grant_id>P30 NS098577</funding_grant_id><funding_grant_id>R01 AG068319</funding_grant_id><funding_grant_id>U19AG032438</funding_grant_id><funding_grant_id>S10 OD025214</funding_grant_id><funding_grant_id>R01 AG046179</funding_grant_id><funding_grant_id>R01AG046179</funding_grant_id><pubmed_authors>Klunk WE</pubmed_authors><pubmed_authors>Gauthier S</pubmed_authors><pubmed_authors>Brooks WS</pubmed_authors><pubmed_authors>Fagan AM</pubmed_authors><pubmed_authors>Wang G</pubmed_authors><pubmed_authors>Bateman RJ</pubmed_authors><pubmed_authors>Hobbs DA</pubmed_authors><pubmed_authors>Higgins I</pubmed_authors><pubmed_authors>Shi X</pubmed_authors><pubmed_authors>Berman SB</pubmed_authors><pubmed_authors>Koeppe R</pubmed_authors><pubmed_authors>Galasko D</pubmed_authors><pubmed_authors>Wallon D</pubmed_authors><pubmed_authors>van Dyck CH</pubmed_authors><pubmed_authors>Dubois B</pubmed_authors><pubmed_authors>Su Y</pubmed_authors><pubmed_authors>Tunali I</pubmed_authors><pubmed_authors>Brosch J</pubmed_authors><pubmed_authors>Chen CD</pubmed_authors><pubmed_authors>Clarnette R</pubmed_authors><pubmed_authors>Masellis M</pubmed_authors><pubmed_authors>Jack C</pubmed_authors><pubmed_authors>Cruchaga C</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>McKay NS</pubmed_authors><pubmed_authors>Jimenez-Velazquez IZ</pubmed_authors><pubmed_authors>Flores S</pubmed_authors><pubmed_authors>Xiong C</pubmed_authors><pubmed_authors>Shcherbinin S</pubmed_authors><pubmed_authors>Mills S</pubmed_authors><pubmed_authors>Pariente J</pubmed_authors><pubmed_authors>Hornbeck R</pubmed_authors><pubmed_authors>Snider BJ</pubmed_authors><pubmed_authors>Salloway S</pubmed_authors><pubmed_authors>Surti G</pubmed_authors><pubmed_authors>DIAN-TU Study Team</pubmed_authors><pubmed_authors>Roberson ED</pubmed_authors><pubmed_authors>Supnet-Bell C</pubmed_authors><pubmed_authors>Pasquier F</pubmed_authors><pubmed_authors>Hsiung R</pubmed_authors><pubmed_authors>Honig LS</pubmed_authors><pubmed_authors>Pontecorvo MJ</pubmed_authors><pubmed_authors>Goate AM</pubmed_authors><pubmed_authors>Perrin RJ</pubmed_authors><pubmed_authors>Clifford DB</pubmed_authors><pubmed_authors>Joseph-Mathurin N</pubmed_authors><pubmed_authors>Masters CL</pubmed_authors><pubmed_authors>McDade E</pubmed_authors><pubmed_authors>Klein G</pubmed_authors><pubmed_authors>McCullough A</pubmed_authors><pubmed_authors>Sanchez-Valle R</pubmed_authors><pubmed_authors>Benzinger TLS</pubmed_authors><pubmed_authors>Gordon B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Longitudinal head-to-head comparison of &amp;lt;sup&amp;gt;11&amp;lt;/sup&amp;gt;C-PiB and &amp;lt;sup&amp;gt;18&amp;lt;/sup&amp;gt;F-florbetapir PET in a Phase 2/3 clinical trial of anti-amyloid-β monoclonal antibodies in dominantly inherited Alzheimer's disease.</name><description>&lt;h4>Purpose&lt;/h4>Pittsburgh Compound-B (&lt;sup>11&lt;/sup>C-PiB) and &lt;sup>18&lt;/sup>F-florbetapir are amyloid-β (Aβ) positron emission tomography (PET) radiotracers that have been used as endpoints in Alzheimer's disease (AD) clinical trials to evaluate the efficacy of anti-Aβ monoclonal antibodies. However, comparing drug effects between and within trials may become complicated if different Aβ radiotracers were used. To study the consequences of using different Aβ radiotracers to measure Aβ clearance, we performed a head-to-head comparison of &lt;sup>11&lt;/sup>C-PiB and &lt;sup>18&lt;/sup>F-florbetapir in a Phase 2/3 clinical trial of anti-Aβ monoclonal antibodies.&lt;h4>Methods&lt;/h4>Sixty-six mutation-positive participants enrolled in the gantenerumab and placebo arms of the first Dominantly Inherited Alzheime</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jul</publication><modification>2026-05-28T23:12:09.141Z</modification><creation>2024-11-09T11:13:25.052Z</creation></dates><accession>S-EPMC10330155</accession><cross_references><pubmed>37017737</pubmed><doi>10.1007/s00259-023-06209-0</doi></cross_references></HashMap>