<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Johnson M</submitter><funding>Pfizer</funding><funding>NCI NIH HHS</funding><pagination>2517-2526</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9359741</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(12)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>ARRY-382 (PF-07265804) is a selective inhibitor of colony-stimulating factor-1 receptor. We evaluated the safety and preliminary efficacy of ARRY-382 plus pembrolizumab in patients with advanced solid tumors.&lt;h4>Patients and methods&lt;/h4>This was an open-label, multicenter, Phase 1b/2 study (NCT02880371) performed over September 1, 2016 to October 24, 2019. In the Phase 1b dose-escalation, patients with selected advanced solid tumors received ARRY-382 [starting dose 200 mg once daily (QD) orally] plus pembrolizumab [2 mg/kg intravenously (IV) every 3 weeks (Q3W)]. Phase 2 patients had: Pancreatic ductal adenocarcinoma (PDA); programmed cell death protein-1 (PD-1)/PD-ligand 1 (PD-L1) inhibitor-refractory (PD-1/PD-L1 IR) advanced solid tumors; or platinum-resistant ovarian can</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pubmed_title>ARRY-382 in Combination with Pembrolizumab in Patients with Advanced Solid Tumors: Results from a Phase 1b/2 Study.</pubmed_title><pmcid>PMC9359741</pmcid><funding_grant_id>P30 CA054174</funding_grant_id><funding_grant_id>P30CA054174</funding_grant_id><pubmed_authors>Rothenberg SM</pubmed_authors><pubmed_authors>Kunk PR</pubmed_authors><pubmed_authors>Lewis K</pubmed_authors><pubmed_authors>Sarantopoulos J</pubmed_authors><pubmed_authors>Lee P</pubmed_authors><pubmed_authors>Johnson M</pubmed_authors><pubmed_authors>Golden A</pubmed_authors><pubmed_authors>Sukari A</pubmed_authors><pubmed_authors>Dudek AZ</pubmed_authors><pubmed_authors>Goldman JW</pubmed_authors><pubmed_authors>Call J</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Gainor JF</pubmed_authors><pubmed_authors>Harney A</pubmed_authors></additional><is_claimable>false</is_claimable><name>ARRY-382 in Combination with Pembrolizumab in Patients with Advanced Solid Tumors: Results from a Phase 1b/2 Study.</name><description>&lt;h4>Purpose&lt;/h4>ARRY-382 (PF-07265804) is a selective inhibitor of colony-stimulating factor-1 receptor. We evaluated the safety and preliminary efficacy of ARRY-382 plus pembrolizumab in patients with advanced solid tumors.&lt;h4>Patients and methods&lt;/h4>This was an open-label, multicenter, Phase 1b/2 study (NCT02880371) performed over September 1, 2016 to October 24, 2019. In the Phase 1b dose-escalation, patients with selected advanced solid tumors received ARRY-382 [starting dose 200 mg once daily (QD) orally] plus pembrolizumab [2 mg/kg intravenously (IV) every 3 weeks (Q3W)]. Phase 2 patients had: Pancreatic ductal adenocarcinoma (PDA); programmed cell death protein-1 (PD-1)/PD-ligand 1 (PD-L1) inhibitor-refractory (PD-1/PD-L1 IR) advanced solid tumors; or platinum-resistant ovarian can</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jun</publication><modification>2026-05-28T03:42:02.705Z</modification><creation>2025-04-04T20:21:53.91Z</creation></dates><accession>S-EPMC9359741</accession><cross_references><pubmed>35302585</pubmed><doi>10.1158/1078-0432.CCR-21-3009</doi></cross_references></HashMap>