A Study to Evaluate the Efficacy and Safety of TAK-906 in Adult Participants With Symptomatic Idiopathic or Diabetic Gastroparesis

clinical trial

Wikidata entity: Q62810737



Quantities

P4135maximum age85
P2899minimum age18
P1132number of participants280

P6099 clinical trial phase ... Q42824440 (phase II clinical trial) phase II clinical trial
P17 country ... Q30 (United States) United States
P17 country ... Q31 (Belgium) Belgium
P17 country ... Q17 (Japan) Japan
P17 country ... Q36 (Poland) Poland
P17 country ... Q38 (Italy) Italy
P582 end time ... 2020-03-30 ???
P31 instance of ... Q30612 (clinical trial) clinical trial
P1050 medical condition ... Q943897 (gastroparesis) gastroparesis
P4844 research intervention ... Q42038 (maleic acid) maleic acid
P6153 research site ... Q1130172 (Mayo Clinic) Mayo Clinic
P6153 research site ... Q4897536 (Beth Israel Deaconess Medical Center) Beth Israel Deaconess Medical Center
P6153 research site ... Q30254036 (Temple University Hospital) Temple University Hospital
P6153 research site ... Q30270033 (PMG Research) PMG Research
P6153 research site ... Q33526980 (University of Kansas Medical Center) University of Kansas Medical Center
P6153 research site ... Q50035610 (Precision Research Institute) Precision Research Institute
P6153 research site ... Q175241 (University of Antwerp) University of Antwerp
P6153 research site ... Q230492 (University of Michigan) University of Michigan
P6153 research site ... Q691851 (University of Naples Federico II) University of Naples Federico II
P580 start time ... 2018-10-17 ???
P8363 study type ... Q78089383 (interventional study) interventional study
P1476 title Monolingualtext A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2b Study to Evaluate the Efficacy and Safety of Twice-Daily Oral Administration of a Peripherally Acting Dopamine Receptor D2/D3 Antagonist, TAK-906 for the Treatment of Adult Subjects With Symptomatic Idiopathic or Diabetic Gastroparesis ???

External Ids
P3098ClinicalTrials.gov IDNCT03544229

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