<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Benderski K</submitter><funding>European Research Council</funding><funding>Deutsche Forschungsgemeinschaft (German Research Foundation)</funding><pagination>1163-1172</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12373501</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(8)</volume><pubmed_abstract>Multi-drug nanomedicine is gaining momentum for co-delivering more than one drug to the same site at the same time. Our analysis of 273 pre-clinical tumour growth inhibition studies shows that multi-drug nanotherapy outperforms single-drug therapy, multi-drug combination therapy, and single-drug nanotherapy by 43, 29 and 30%, respectively. Combination nanotherapy also results in the best overall survival rates, with 56% of studies demonstrating complete or partial survival, versus 20-37% for control regimens. Within the multi-drug nanomedicine groups, we analysed the effect of (co-)administration schedule and strategy, passive versus active targeting, nanocarrier material and the type of therapeutic agent. Most importantly, it was found that co-encapsulating two different drugs in the same</pubmed_abstract><journal>Nature nanotechnology</journal><pubmed_title>Analysis of multi-drug cancer nanomedicine.</pubmed_title><pmcid>PMC12373501</pmcid><funding_grant_id>KFO344</funding_grant_id><funding_grant_id>864121</funding_grant_id><funding_grant_id>SFB1066</funding_grant_id><pubmed_authors>Benderski K</pubmed_authors><pubmed_authors>Lammers T</pubmed_authors><pubmed_authors>Sofias AM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Analysis of multi-drug cancer nanomedicine.</name><description>Multi-drug nanomedicine is gaining momentum for co-delivering more than one drug to the same site at the same time. Our analysis of 273 pre-clinical tumour growth inhibition studies shows that multi-drug nanotherapy outperforms single-drug therapy, multi-drug combination therapy, and single-drug nanotherapy by 43, 29 and 30%, respectively. Combination nanotherapy also results in the best overall survival rates, with 56% of studies demonstrating complete or partial survival, versus 20-37% for control regimens. Within the multi-drug nanomedicine groups, we analysed the effect of (co-)administration schedule and strategy, passive versus active targeting, nanocarrier material and the type of therapeutic agent. Most importantly, it was found that co-encapsulating two different drugs in the same</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-05-09T10:39:38.614Z</modification><creation>2026-04-08T00:48:19.152Z</creation></dates><accession>S-EPMC12373501</accession><cross_references><pubmed>40374796</pubmed><doi>10.1038/s41565-025-01932-1</doi></cross_references></HashMap>