Drugs / Lafutidine

Trials 6 · a red edge is where a trial was stopped

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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

NCT02581696

NCT01499368

NCT00229424

NCT02759224

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