Drugs / Lafutidine

Trials 6

20052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 13 trials
Phase 1 NCT02759224 Apr → Jul 2016 gastric ulcer Boryung Pharmaceutical Co., Ltd Completed No outcome recorded
Phase 1 NCT02581696 Aug → Nov 2015 peptic ulcer disease Boryung Pharmaceutical Co., Ltd Completed No outcome recorded
Phase 1 NCT02658864 Apr → Jun 2005 chronic gastritis Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Completed No outcome recorded
Phase 32 trials
Phase 3 NCT01499368 Nov 2011 → Nov 2012 esophagitis Boryung Pharmaceutical Co., Ltd Completed No outcome recorded
Phase 3 NCT00229424 Apr 2005 → Oct 2006 gastroesophageal reflux disease Taiho Pharmaceutical Co., Ltd. Completed No outcome recorded
Phase 41 trial
Phase 4 NCT02703896 Jan 2012 lung disorder King Saud University Completed No outcome recorded

Evidence & citations 6 cited values

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

FieldValueCited text
Known as Lafutidine “Group S (lafutidine 10 mg)” NCT02703896 ↗
5

NCT00229424 ↗

NCT02581696 ↗

NCT02759224 ↗

NCT01499368 ↗

NCT02658864 ↗

Known as Lafutidina ChEMBL registry synonym — accepted as the source's own label CHEMBL1742461 ↗
Action Inhibit “Histamine H2 receptor antagonist” CHEMBL1742461 ↗
Modality Small molecule — CHEMBL1742461 ↗
Route Oral “Oral administration of lafutidine by 20mg/day along with famotidine placebo” NCT00229424 ↗
Target HRH2 “Histamine H2 receptor antagonist” CHEMBL1742461 ↗