<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>4(4)</volume><submitter>Zhu E</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>IL-13 plays a key role in the induction and perpetuation of type 2 immune responses associated with the development of atopic dermatitis and other chronic inflammatory diseases. mAbs targeting IL-13 have demonstrated efficacy in IL-13-driven diseases; however, current therapeutics require dosing every 2 to 4 weeks, resulting in significant injection burden for patients. APG777 is a humanized, IgG1 IL-13-targeting mAb that has been engineered to have an optimized pharmacokinetic profile, allowing for less frequent dosing.&lt;h4>Objective&lt;/h4>We sought to investigate the &lt;i>in vitro&lt;/i> potency and &lt;i>in vivo&lt;/i> pharmacokinetics of APG777.&lt;h4>Methods&lt;/h4>The affinity of APG777 was characterized using surface plasmon resonance; the half-maximal inhibitory concentration (IC&lt;su</pubmed_abstract><journal>The journal of allergy and clinical immunology. Global</journal><pagination>100545</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12419008</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>&amp;lt;i&amp;gt;In vitro&amp;lt;/i&amp;gt; potency and pharmacokinetics of APG777, a novel anti-IL-13 mAb.</pubmed_title><pmcid>PMC12419008</pmcid><pubmed_authors>Prentice H</pubmed_authors><pubmed_authors>Dabora R</pubmed_authors><pubmed_authors>Oh J</pubmed_authors><pubmed_authors>Shaheen H</pubmed_authors><pubmed_authors>Dambkowski CL</pubmed_authors><pubmed_authors>Zhu E</pubmed_authors><pubmed_authors>Gandhi NA</pubmed_authors><pubmed_authors>Wickman G</pubmed_authors><pubmed_authors>Dillinger L</pubmed_authors></additional><is_claimable>false</is_claimable><name>&amp;lt;i&amp;gt;In vitro&amp;lt;/i&amp;gt; potency and pharmacokinetics of APG777, a novel anti-IL-13 mAb.</name><description>&lt;h4>Background&lt;/h4>IL-13 plays a key role in the induction and perpetuation of type 2 immune responses associated with the development of atopic dermatitis and other chronic inflammatory diseases. mAbs targeting IL-13 have demonstrated efficacy in IL-13-driven diseases; however, current therapeutics require dosing every 2 to 4 weeks, resulting in significant injection burden for patients. APG777 is a humanized, IgG1 IL-13-targeting mAb that has been engineered to have an optimized pharmacokinetic profile, allowing for less frequent dosing.&lt;h4>Objective&lt;/h4>We sought to investigate the &lt;i>in vitro&lt;/i> potency and &lt;i>in vivo&lt;/i> pharmacokinetics of APG777.&lt;h4>Methods&lt;/h4>The affinity of APG777 was characterized using surface plasmon resonance; the half-maximal inhibitory concentration (IC&lt;su</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-05-26T11:08:24.596Z</modification><creation>2026-05-24T03:07:06.316Z</creation></dates><accession>S-EPMC12419008</accession><cross_references><pubmed>40933957</pubmed><doi>10.1016/j.jacig.2025.100545</doi></cross_references></HashMap>