Drugs / Tasisulam

Trials 13 · a red edge is where a trial was stopped

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 17 trials
Phase 1 NCT01209832 Sep 2010 → Jan 2011 cancer of unknown primary site Eli Lilly and Company Terminated No outcome recorded
Phase 1 NCT01185548 Jul → Dec 2010 lymphoma Eli Lilly and Company Terminated No outcome recorded
Phase 1 NCT01214668 Jan 2009 → Feb 2012 cancer Eli Lilly and Company Completed No outcome recorded
Phase 1 NCT00718159 Aug 2008 → Dec 2011 acute myeloid leukemia, essential thrombocythemia Eli Lilly and Company Completed No outcome recorded
Phase 1 NCT01258348 Jul 2008 → Feb 2012 renal cell carcinoma Eli Lilly and Company Completed No outcome recorded
Phase 1 NCT01284335 Jul 2008 → Oct 2012 cancer Eli Lilly and Company Terminated No outcome recorded
Phase 1 NCT01215916 Feb 2008 → Dec 2011 cancer Eli Lilly and Company Completed No outcome recorded
Phase 25 trials
Phase 2 NCT00992225 Sep 2009 → Apr 2011 breast cancer Eli Lilly and Company Completed No outcome recorded
Phase 2 NCT00490451 Aug 2007 → Feb 2010 soft tissue sarcoma Eli Lilly and Company Completed No outcome recorded
Phase 2 NCT00428610 Feb 2007 → Feb 2011 fallopian tube cancer, ovarian cancer, primary peritoneal carcinoma Eli Lilly and Company Completed No outcome recorded
Phase 2 NCT00383292 Nov 2006 → Sep 2011 metastatic melanoma Eli Lilly and Company Completed No outcome recorded
Phase 2 NCT00363766 Sep 2006 → Oct 2008 non-small cell lung carcinoma Eli Lilly and Company Completed No outcome recorded
Phase 31 trial
Phase 3 NCT01006252 Dec 2009 → Mar 2011 melanoma Eli Lilly and Company Terminated No outcome recorded

Evidence & citations 9 cited values

Every value below carries the sentence it was read from. 14 sources stand behind the page.

FieldValueCited text
Known as Tasisulam ClinicalTrials.gov intervention name — accepted as the source's own label NCT01006252
3

NCT00383292

NCT01185548

NCT01209832

Known as LY-573636.NA ChEMBL registry synonym — accepted as the source's own label CHEMBL2110587
Known as LY573636 ClinicalTrials.gov intervention name — accepted as the source's own label NCT00718159
6

NCT00428610

NCT01215916

NCT01214668

NCT01284335

NCT00490451

NCT00363766

Known as LY573636-sodium “The goal of this study is to determine the dose of LY573636-sodium (hereafter referred to as LY573636) that can be administered safely in combination with liposomal doxorubicin...” NCT01214668
5

“The primary objective is to estimate the time to progressive disease for patients who receive LY573636-sodium (hereafter referred to as LY573636) after two previous treatments...” NCT00363766

“The primary purpose of the study is to estimate the time from the first dose of LY573636-sodium (hereafter referred to as LY573636) to the date your physician determines that...” NCT00490451

LY573636-sodium (LY573636) is administered every 28 days until disease progression or other criteria for participant discontinuation are met.” NCT00428610

NCT01258348

NCT00992225

Known as TASISULAM SODIUM ChEMBL registry synonym — accepted as the source's own label CHEMBL2110587
Action Inhibit inhibitor of CYP2C9” NCT01185548
Modality Small molecule CHEMBL2110587
Route Intravenous “Patients will receive an intravenous infusion of study drug once every 21 days.” NCT00363766
Target CYP2C9 “inhibitor of CYP2C9NCT01185548