QTc Study GSK573719+GW642444
clinical trial
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Summary
QTc Study GSK573719+GW642444 is a clinical trial[1].
Key Facts
- QTc Study GSK573719+GW642444 is in the country of United Kingdom[2].
- QTc Study GSK573719+GW642444's instance of is recorded as clinical trial[3].
- QTc Study GSK573719+GW642444's start time is recorded as +2011-12-19T00:00:00Z[4].
- QTc Study GSK573719+GW642444's end time is recorded as +2012-06-05T00:00:00Z[5].
- QTc Study GSK573719+GW642444's sponsor is recorded as GSK[6].
- QTc Study GSK573719+GW642444's main subject is recorded as chronic obstructive pulmonary disease[7].
- QTc Study GSK573719+GW642444's main subject is recorded as tolerability[8].
- QTc Study GSK573719+GW642444's main subject is recorded as safety[9].
- QTc Study GSK573719+GW642444's main subject is recorded as pharmacokinetics[10].
- QTc Study GSK573719+GW642444's number of participants is recorded as {'unit': '1', 'amount': '+100'}[11].
- QTc Study GSK573719+GW642444's title is recorded as A Randomised, Placebo-controlled, Incomplete Block, Four Period Crossover , Repeat Dose Study to Evaluate the Effect of the Inhaled GSK573719/Vilanterol Combination and GSK573719 Monotherapy on Electrocardiographic Parameters, With Moxifloxacin as a Positive Control, in Healthy Subjects.[12].
- QTc Study GSK573719+GW642444's minimum age is recorded as {'unit': 'http://www.wikidata.org/entity/Q577', 'amount': '+18'}[13].
- QTc Study GSK573719+GW642444's ClinicalTrials.gov ID is recorded as NCT01521377[14].
- QTc Study GSK573719+GW642444's maximum age is recorded as {'unit': 'http://www.wikidata.org/entity/Q577', 'amount': '+65'}[15].
- QTc Study GSK573719+GW642444's research intervention is recorded as moxifloxacin[16].
- QTc Study GSK573719+GW642444's clinical trial phase is recorded as phase I clinical trial[17].
- QTc Study GSK573719+GW642444's research site is recorded as GSK[18].
- QTc Study GSK573719+GW642444's research subject recruitment status is recorded as completed[19].
- QTc Study GSK573719+GW642444's study type is recorded as interventional study[20].