<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(19)</volume><submitter>Koehler RC</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The Stroke Preclinical Assessment Network tested 6 therapeutic interventions initiated at the time of reperfusion after focal ischemic stroke in young mice, aging mice, obese mice, and spontaneously hypertensive rats. This randomized, controlled trial was conducted across 6 sites with concealed treatment and blinded neurobehavior assessments. The trial had an adaptive design with preset levels of efficacy and futility interrogated after each of 4 stages. The primary outcome was turning preference on the corner test at 1 month. The PARP (poly(ADP-ribose) polymerase) inhibitor, veliparib, was considered futile after the second stage when pooling all animal models (&lt;i>n&lt;/i>=231 veliparib; &lt;i>n&lt;/i>=344 placebo).&lt;h4>Methods&lt;/h4>A secondary analysis was performed to evaluate v</pubmed_abstract><journal>Journal of the American Heart Association</journal><pagination>e040914</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12684482</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Multicenter Stroke Preclinical Assessment Network Analysis of Cardiovascular Risk Factor Subgroups Treated With the Poly(ADP-Ribose) Polymerase Inhibitor Veliparib.</pubmed_title><pmcid>PMC12684482</pmcid><pubmed_authors>Nagarkatti KA</pubmed_authors><pubmed_authors>Siddiqui S</pubmed_authors><pubmed_authors>Bibic A</pubmed_authors><pubmed_authors>Hyder F</pubmed_authors><pubmed_authors>Wang K</pubmed_authors><pubmed_authors>Erdogan TD</pubmed_authors><pubmed_authors>Shi Y</pubmed_authors><pubmed_authors>Thedens D</pubmed_authors><pubmed_authors>McCullough LD</pubmed_authors><pubmed_authors>Nagarkatti K</pubmed_authors><pubmed_authors>Goh A</pubmed_authors><pubmed_authors>Akhter K</pubmed_authors><pubmed_authors>Imai T</pubmed_authors><pubmed_authors>Jin X</pubmed_authors><pubmed_authors>Ayata C</pubmed_authors><pubmed_authors>Beatty HE</pubmed_authors><pubmed_authors>Bedirian K</pubmed_authors><pubmed_authors>Avery BD</pubmed_authors><pubmed_authors>Dawson T</pubmed_authors><pubmed_authors>Dawson V</pubmed_authors><pubmed_authors>Lo E</pubmed_authors><pubmed_authors>Kumskova M</pubmed_authors><pubmed_authors>Kimberly WT</pubmed_authors><pubmed_authors>Lamb J</pubmed_authors><pubmed_authors>Chauhan A</pubmed_authors><pubmed_authors>Diaz-Perez S</pubmed_authors><pubmed_authors>Van Leyen K</pubmed_authors><pubmed_authors>Sansing LH</pubmed_authors><pubmed_authors>de Morais AL</pubmed_authors><pubmed_authors>Aronowski J</pubmed_authors><pubmed_authors>Immakavar E</pubmed_authors><pubmed_authors>Yu L</pubmed_authors><pubmed_authors>Nisar M</pubmed_authors><pubmed_authors>Herman AL</pubmed_authors><pubmed_authors>Lyden PD</pubmed_authors><pubmed_authors>Dhanesha N</pubmed_authors><pubmed_authors>Qin T</pubmed_authors><pubmed_authors>Avery B</pubmed_authors><pubmed_authors>Obertas L</pubmed_authors><pubmed_authors>Dawson TM</pubmed_authors><pubmed_authors>Mandeville JB</pubmed_authors><pubmed_authors>Boisserand LSB</pubmed_authors><pubmed_authors>Sanganahalli BG</pubmed_authors><pubmed_authors>Johnson C</pubmed_authors><pubmed_authors>Chauhan AK</pubmed_authors><pubmed_authors>Mihailovic JM</pubmed_authors><pubmed_authors>Karuppagounder SS</pubmed_authors><pubmed_authors>Whittier JPW</pubmed_authors><pubmed_authors>Koehler RC</pubmed_authors><pubmed_authors>Hess DC</pubmed_authors><pubmed_authors>SPAN investigators [Link]</pubmed_authors><pubmed_authors>Smith C</pubmed_authors><pubmed_authors>Diniz MA</pubmed_authors><pubmed_authors>Lannon S</pubmed_authors><pubmed_authors>Patel RB</pubmed_authors><pubmed_authors>Velazquez SE</pubmed_authors><pubmed_authors>Dawson VL</pubmed_authors><pubmed_authors>Leira EC</pubmed_authors><pubmed_authors>Kamat PK</pubmed_authors><pubmed_authors>Arbab AS</pubmed_authors><pubmed_authors>Jaroslaw Aronowski MD</pubmed_authors><pubmed_authors>Dhandapani KM</pubmed_authors><pubmed_authors>Huang S</pubmed_authors><pubmed_authors>Chen MH</pubmed_authors><pubmed_authors>Cao S</pubmed_authors><pubmed_authors>Arai K</pubmed_authors><pubmed_authors>Khan MB</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multicenter Stroke Preclinical Assessment Network Analysis of Cardiovascular Risk Factor Subgroups Treated With the Poly(ADP-Ribose) Polymerase Inhibitor Veliparib.</name><description>&lt;h4>Background&lt;/h4>The Stroke Preclinical Assessment Network tested 6 therapeutic interventions initiated at the time of reperfusion after focal ischemic stroke in young mice, aging mice, obese mice, and spontaneously hypertensive rats. This randomized, controlled trial was conducted across 6 sites with concealed treatment and blinded neurobehavior assessments. The trial had an adaptive design with preset levels of efficacy and futility interrogated after each of 4 stages. The primary outcome was turning preference on the corner test at 1 month. The PARP (poly(ADP-ribose) polymerase) inhibitor, veliparib, was considered futile after the second stage when pooling all animal models (&lt;i>n&lt;/i>=231 veliparib; &lt;i>n&lt;/i>=344 placebo).&lt;h4>Methods&lt;/h4>A secondary analysis was performed to evaluate v</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Oct</publication><modification>2026-06-06T00:04:35.277Z</modification><creation>2026-05-23T03:13:25.434Z</creation></dates><accession>S-EPMC12684482</accession><cross_references><pubmed>40996065</pubmed><doi>10.1161/JAHA.124.040914</doi></cross_references></HashMap>