<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Chirinos J</submitter><funding>NCATS NIH HHS</funding><pubmed_abstract>Background Abnormal cellular lipid metabolism appears to underlie SARS-CoV-2 cytotoxicity and may involve inhibition of peroxisome proliferator activated receptor alpha (PPARα). Fenofibrate, a PPAR-α activator, modulates cellular lipid metabolism. Fenofibric acid has also been shown to affect the dimerization of angiotensin-converting enzyme 2, the cellular receptor for SARS-CoV-2. Fenofibrate and fenofibric acid have been shown to inhibit SARS-CoV-2 replication in cell culture systems &lt;i>in vitro&lt;/i> . Methods We randomly assigned 701 participants with COVID-19 within 14 days of symptom onset to 145 mg of fenofibrate (nanocrystal formulation with dose adjustment for renal function or dose-equivalent preparations of micronized fenofibrate or fenofibric acid) vs. placebo for 10 days, in a d</pubmed_abstract><journal>Research square</journal><pagination>rs.3.rs-1933913</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9387540</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A Randomized Trial of Lipid Metabolism Modulation with Fenofibrate for Acute Coronavirus Disease 2019.</pubmed_title><pmcid>PMC9387540</pmcid><funding_grant_id>U01 TR003734</funding_grant_id><pubmed_authors>Giamarellos-Bourboulis E</pubmed_authors><pubmed_authors>Gomez-Laiton E</pubmed_authors><pubmed_authors>Sanchez G</pubmed_authors><pubmed_authors>Greczylo C</pubmed_authors><pubmed_authors>Hernandez JR</pubmed_authors><pubmed_authors>Villavicencio-Carranza M</pubmed_authors><pubmed_authors>Danos WL</pubmed_authors><pubmed_authors>Perez-Mayorga M</pubmed_authors><pubmed_authors>Milionis H</pubmed_authors><pubmed_authors>Katsaounou P</pubmed_authors><pubmed_authors>Castro-Callirgos C</pubmed_authors><pubmed_authors>Greene K</pubmed_authors><pubmed_authors>Saldarriaga MC</pubmed_authors><pubmed_authors>Chittams J</pubmed_authors><pubmed_authors>Cure-Cure C</pubmed_authors><pubmed_authors>Sharkoski T</pubmed_authors><pubmed_authors>Giraldo MC</pubmed_authors><pubmed_authors>Rosado-Santander N</pubmed_authors><pubmed_authors>Moghnieh R</pubmed_authors><pubmed_authors>Pereyra R</pubmed_authors><pubmed_authors>Poulakou G</pubmed_authors><pubmed_authors>Ayala-Garcia R</pubmed_authors><pubmed_authors>Arbanil H</pubmed_authors><pubmed_authors>Rodriguez-Mori J</pubmed_authors><pubmed_authors>Dimitroulis I</pubmed_authors><pubmed_authors>Gutierrez C</pubmed_authors><pubmed_authors>Pourmussa B</pubmed_authors><pubmed_authors>Accini-Mendoza J</pubmed_authors><pubmed_authors>Valdivia-Vega R</pubmed_authors><pubmed_authors>Sympardi S</pubmed_authors><pubmed_authors>Pariona M</pubmed_authors><pubmed_authors>Vlachopoulos C</pubmed_authors><pubmed_authors>Sweitzer N</pubmed_authors><pubmed_authors>Gonzalez-Hernandez L</pubmed_authors><pubmed_authors>Chirinos J</pubmed_authors><pubmed_authors>Putt M</pubmed_authors><pubmed_authors>Lopez-Jaramillo P</pubmed_authors><pubmed_authors>Angeliki R</pubmed_authors><pubmed_authors>Davila-Del-Carpio G</pubmed_authors><pubmed_authors>Cohen J</pubmed_authors><pubmed_authors>Salman O</pubmed_authors><pubmed_authors>Medina C</pubmed_authors><pubmed_authors>Carrasco RA</pubmed_authors><pubmed_authors>Alexiou Z</pubmed_authors><pubmed_authors>Bizri A</pubmed_authors><pubmed_authors>Andrade-Villanueva J</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Randomized Trial of Lipid Metabolism Modulation with Fenofibrate for Acute Coronavirus Disease 2019.</name><description>Background Abnormal cellular lipid metabolism appears to underlie SARS-CoV-2 cytotoxicity and may involve inhibition of peroxisome proliferator activated receptor alpha (PPARα). Fenofibrate, a PPAR-α activator, modulates cellular lipid metabolism. Fenofibric acid has also been shown to affect the dimerization of angiotensin-converting enzyme 2, the cellular receptor for SARS-CoV-2. Fenofibrate and fenofibric acid have been shown to inhibit SARS-CoV-2 replication in cell culture systems &lt;i>in vitro&lt;/i> . Methods We randomly assigned 701 participants with COVID-19 within 14 days of symptom onset to 145 mg of fenofibrate (nanocrystal formulation with dose adjustment for renal function or dose-equivalent preparations of micronized fenofibrate or fenofibric acid) vs. placebo for 10 days, in a d</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2026-04-08T11:10:47.407Z</modification><creation>2025-04-19T22:46:06.349Z</creation></dates><accession>S-EPMC9387540</accession><cross_references><pubmed>35982675</pubmed><doi>10.21203/rs.3.rs-1933913/v1</doi></cross_references></HashMap>