<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kim ST</submitter><funding>Korean Health Technology R and D Project, ministru of Health and &amp;apos;Welfare.</funding><funding>Astra Zeneca Externally sponsored Trial</funding><funding>Skku Excellence in Research Award 2020</funding><pagination>4700-4709</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8974415</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>27(17)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Ceralasertib is a potent and selective oral inhibitor of the serine/threonine protein kinase ataxia telangiectasia and Rad3-related (ATR) protein.&lt;h4>Patients and methods&lt;/h4>Eligible patients with solid tumors, enriched for melanoma, received ceralasertib in combination with a fixed dose of paclitaxel (80 mg/m&lt;sup>2&lt;/sup> on D1, D8, D15) in 28-day cycles. The dose of ceralasertib was escalated to reach an MTD in a rolling 6 design. The starting dose of ceralasertib was 40 mg QD. Fifty-seven patients (33 patients with melanoma who failed prior PD1/L1 treatment) were enrolled in 7 dose cohorts ranging from 40 mg QD to 240 mg BD plus weekly paclitaxel.&lt;h4>Results&lt;/h4>The RP2D was established as ceralasertib 240 mg BD days 1-14 plus paclitaxel 80 mg/m&lt;sup>2&lt;/sup> on D1, D8, D1</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pubmed_title>Phase I Study of Ceralasertib (AZD6738), a Novel DNA Damage Repair Agent, in Combination with Weekly Paclitaxel in Refractory Cancer.</pubmed_title><pmcid>PMC8974415</pmcid><funding_grant_id>JR20C0025</funding_grant_id><pubmed_authors>Park YS</pubmed_authors><pubmed_authors>Berges A</pubmed_authors><pubmed_authors>Smith SA</pubmed_authors><pubmed_authors>Smith C</pubmed_authors><pubmed_authors>Kim KM</pubmed_authors><pubmed_authors>Kim ST</pubmed_authors><pubmed_authors>Hong JY</pubmed_authors><pubmed_authors>Lee J</pubmed_authors><pubmed_authors>Irurzun-Arana I</pubmed_authors><pubmed_authors>Park JO</pubmed_authors><pubmed_authors>Lim HY</pubmed_authors><pubmed_authors>Willis S</pubmed_authors><pubmed_authors>Loembe AB</pubmed_authors><pubmed_authors>Cho H</pubmed_authors><pubmed_authors>Kang WK</pubmed_authors><pubmed_authors>Dean E</pubmed_authors><pubmed_authors>Kozarewa I</pubmed_authors><pubmed_authors>Park SH</pubmed_authors><pubmed_authors>Pierce AJ</pubmed_authors><pubmed_authors>Mortimer P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Phase I Study of Ceralasertib (AZD6738), a Novel DNA Damage Repair Agent, in Combination with Weekly Paclitaxel in Refractory Cancer.</name><description>&lt;h4>Purpose&lt;/h4>Ceralasertib is a potent and selective oral inhibitor of the serine/threonine protein kinase ataxia telangiectasia and Rad3-related (ATR) protein.&lt;h4>Patients and methods&lt;/h4>Eligible patients with solid tumors, enriched for melanoma, received ceralasertib in combination with a fixed dose of paclitaxel (80 mg/m&lt;sup>2&lt;/sup> on D1, D8, D15) in 28-day cycles. The dose of ceralasertib was escalated to reach an MTD in a rolling 6 design. The starting dose of ceralasertib was 40 mg QD. Fifty-seven patients (33 patients with melanoma who failed prior PD1/L1 treatment) were enrolled in 7 dose cohorts ranging from 40 mg QD to 240 mg BD plus weekly paclitaxel.&lt;h4>Results&lt;/h4>The RP2D was established as ceralasertib 240 mg BD days 1-14 plus paclitaxel 80 mg/m&lt;sup>2&lt;/sup> on D1, D8, D1</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2026-07-15T01:28:11.04Z</modification><creation>2024-11-12T18:01:35.501Z</creation></dates><accession>S-EPMC8974415</accession><cross_references><pubmed>33975862</pubmed><doi>10.1158/1078-0432.CCR-21-0251</doi></cross_references></HashMap>