<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>18(3)</volume><submitter>Liu Y</submitter><pubmed_abstract>SC1011 (sufenidone) is a novel pyridone derivative with therapeutic potential for idiopathic pulmonary fibrosis (IPF). Two Phase 1 studies evaluated the safety and pharmacokinetics of single (SAD) and multiple ascending doses (MAD) of SC1011 immediate-release (IR) and modified-release (MR) oral formulations in healthy adult subjects. In Phase 1a, subjects were randomized to receive oral SC1011 IR or placebo in SAD (50 mg-300 mg) or MAD (100 mg and 200 mg) twice daily for 7 days. The Phase 1b study consisted of three treatment groups that received 100, 150, or 200 mg SC1011 MR twice daily for 7 days. SC1011 IR was absorbed rapidly (mean time to maximum concentration, T&lt;sub>max&lt;/sub> ≤ 1 h) and eliminated rapidly (mean terminal half-life, t&lt;sub>1/2&lt;/sub>: 1.23-2.64 h) following 50-300 mg sin</pubmed_abstract><journal>Clinical and translational science</journal><pagination>e70179</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11893723</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Safety, Tolerability, and Pharmacokinetics of SC1011 (Sufenidone), a Novel Antifibrotic Small Molecule, in Phase 1 Studies in Healthy Subjects.</pubmed_title><pmcid>PMC11893723</pmcid><pubmed_authors>Qian H</pubmed_authors><pubmed_authors>Jiang F</pubmed_authors><pubmed_authors>Zan B</pubmed_authors><pubmed_authors>Zhu H</pubmed_authors><pubmed_authors>Du Y</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Zeng Y</pubmed_authors><pubmed_authors>Sun X</pubmed_authors><pubmed_authors>Tang H</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Yang Z</pubmed_authors><pubmed_authors>Ge Z</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Tang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Safety, Tolerability, and Pharmacokinetics of SC1011 (Sufenidone), a Novel Antifibrotic Small Molecule, in Phase 1 Studies in Healthy Subjects.</name><description>SC1011 (sufenidone) is a novel pyridone derivative with therapeutic potential for idiopathic pulmonary fibrosis (IPF). Two Phase 1 studies evaluated the safety and pharmacokinetics of single (SAD) and multiple ascending doses (MAD) of SC1011 immediate-release (IR) and modified-release (MR) oral formulations in healthy adult subjects. In Phase 1a, subjects were randomized to receive oral SC1011 IR or placebo in SAD (50 mg-300 mg) or MAD (100 mg and 200 mg) twice daily for 7 days. The Phase 1b study consisted of three treatment groups that received 100, 150, or 200 mg SC1011 MR twice daily for 7 days. SC1011 IR was absorbed rapidly (mean time to maximum concentration, T&lt;sub>max&lt;/sub> ≤ 1 h) and eliminated rapidly (mean terminal half-life, t&lt;sub>1/2&lt;/sub>: 1.23-2.64 h) following 50-300 mg sin</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2025-04-26T02:41:01.958Z</modification><creation>2025-04-06T10:36:33.504Z</creation></dates><accession>S-EPMC11893723</accession><cross_references><pubmed>40065557</pubmed><doi>10.1111/cts.70179</doi></cross_references></HashMap>