Drugs / Oltipraz

Trials 4

2000200120022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 11 trial
Phase 1 NCT00006457 Aug 2000 → Apr 2004 lung cancer Northwestern University Completed No outcome recorded
Phase 22 trials · 1 met primary
Phase 2 NCT01373554 May 2011 → Jun 2013 NAFLD1 PharmaKing Completed Met primary
Phase 2 NCT00956098 Feb 2006 → Feb 2007 cirrhosis of liver, fibrotic liver disease HK inno.N Corporation Completed No outcome recorded
Phase 31 trial
Phase 3 NCT02068339 Feb 2014 → Feb 2016 NAFLD1 PharmaKing Completed No outcome recorded
Comparator or background therapy1 trial
Phase 3 NCT04142749 Comparator Nov 2019 → Sep 2022 NAFLD1 PharmaKing Completed No outcome recorded

Evidence & citations 8 cited values

Every value below carries the sentence it was read from. 7 sources stand behind the page.

FieldValueCited text
Known as Oltipraz ClinicalTrials.gov intervention name — accepted as the source's own label NCT04142749 ↗
4

NCT01373554 ↗

NCT00006457 ↗

NCT02068339 ↗

NCT00956098 ↗

Known as 5-(2-pyrazinyl)-4-methyl-1,2-dithiol-3-thione “Oltipraz \[5-(2-pyrazinyl)-4-methyl-1,2-dithiol-3-thione\] has been extensively studied as a cancer chemopreventive agent.” NCT00956098 ↗
Known as NSC-347901 ChEMBL registry synonym — accepted as the source's own label CHEMBL178459 ↗
Action Inhibit “Oltipraz is a synthetic dithiolethione with an antisteatotic effect by inhibiting the activity of liver X receptor alpha (LXR-α).” PMID 28225186 ↗ Feb 2017
Modality Small molecule “Oltipraz is a synthetic dithiolethione” PMID 28225186 ↗ Feb 2017
Route Oral “Patients receive low-dose oral oltipraz weekly.” NCT00006457 ↗
Target S6K1 “modulation of S6K1 by oltipraz inhibited the development of insulin resistance and hyperglycemia through the AMPK-S6K1 pathway” NCT04142749 ↗
Target SREBP-1c “Oltipraz inhibits fatty acid synthesis through AMPK-S6K1 pathway and LXRg-SREBP-1c pathway in liver.” NCT04142749 ↗