Drugs / VERUCERFONT

Trials 9 · a red edge is where a trial was stopped

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 15 trials
Phase 1 NCT02349503 Feb → Oct 2015 classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Neurocrine Biosciences Withdrawn No outcome recorded
Phase 1 NCT00539136 Oct 2007 → Mar 2008 GlaxoSmithKline Completed No outcome recorded
Phase 1 NCT00513565 Sep 2007 → May 2009 mixed anxiety and depressive disorder GlaxoSmithKline Completed No outcome recorded
Phase 1 NCT00555139 Mar 2007 → Jan 2008 social phobia GlaxoSmithKline Completed No outcome recorded
Phase 1 NCT00426608 Oct 2006 → Jan 2007 GlaxoSmithKline Completed No outcome recorded
Phase 24 trials
Phase 2 NCT01814332 Jan 2010 → Jun 2014 post-traumatic stress disorder VA Office of Research and Development Completed No outcome recorded
Phase 2 NCT01018992 Dec 2009 → Aug 2014 post-traumatic stress disorder Emory University Completed No outcome recorded
Phase 2 NCT00733980 Oct 2008 → Jun 2010 major depressive disorder GlaxoSmithKline Completed No outcome recorded
Phase 2 NCT00511563 Aug 2007 → Nov 2012 irritable bowel syndrome GlaxoSmithKline Withdrawn No outcome recorded
Also used as a comparator or background therapy in 1 trial
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 2 NCT01187511 Comparator Jan 2010 → Sep 2015 alcohol dependence National Institute on Alcohol Abuse and Alcoholism (NIAAA) Completed No outcome recorded

Evidence & citations 8 cited values

Every value below carries the sentence it was read from. 12 sources stand behind the page.

FieldValueCited text
Known as VERUCERFONT ChEMBL registry synonym — accepted as the source's own label CHEMBL1287935
Known as GSK-561679A ChEMBL registry synonym — accepted as the source's own label CHEMBL1287935
Known as GSK561679 “Subjects will receive single doses of GSK561679, lorazepam, or placebo at each treatment session.” NCT00513565
8

NCT00426608

NCT01187511

NCT00539136

NCT00555139

NCT00733980

NCT01814332

NCT01018992

NCT00511563

Known as NBI-77860 ClinicalTrials.gov intervention name — accepted as the source's own label NCT02349503
Action Inhibit “Two CRF-1 antagonists GSK561679 and GW876008” NCT00511563
Modality Small molecule CHEMBL1287935
Route Oral “GSK561679, oral administration, 350mg/day, 6 week administration” NCT01018992
Target CRHR1 “GSK561679, a novel CRHR1 receptor antagonist” PMID 24950747 Jun 2014