I.E.C. Consultants
Bangalore, 560003, India
NCT Number: NCT03215875
This study will evaluate the effects of a high-fat meal (food effect) on the bioavailability and pharmacokinetics of 60mg ER Torsemide tablet after single dose oral administration in healthy volunteers. The study will be conducted as a two-sequence to period crossover study to compare 60mg ER Torsemide ER bioavailability under fed and fasting conditions. 60mg ER torsemide is a new strength and dosage form.
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Notify Me18 year–45 year
Male
Interventional
Phase 1
Bangalore, 560003, India
Immediate Release (IR) Torsemide is a highly effective natriuretic drug but its short duration of action is a major drawback, which allows significant post-dose sodium retention, and as consequence, limits salt loss in patients with heart failure unless dietary salt intake is severely restricted. Extended Release (ER) torsemide is being developed to address this drawback by prolonging the duration of action to increase sodium excretion even in patients who consume high salt diet. Since 60mg ER torsemide is a new strength and dosage form, this study will test 60mg ER torsemide for a food effect in healthy volunteers who are either fasting or consuming a high-fat meal (fed). The primary endpoint of the study is full pharmacokinetics measurements after a single dose of 60mg ER torsemide. The secondary endpoints are 24h sodium excretion and total urinary excretion.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
60mg ER Torsemide will be given after high fat, high-calorie meal
Other names: High fat/high-calorie fed conditions
60mg ER Torsemide will be given after overnight fasting
Other names: Fasting conditions
Time frame: 36 hours
Peak plasma concentration (Cmax) (ng/ml) in fed and fasting conditions
Time frame: 36 hours
Area under the plasma concentration versus time curve (AUC) (hr/ng/ml) in fed and fasting conditions
Time frame: 36 hours
torsemide will be measured in urine over 36 hours post-dose (microgram/min)
Time frame: 36 hours
36-hour sodium excretion will be measure (mmol/min)
Sarfez Pharmaceuticals, Inc.
Industry
A Randomized, Balanced, Single Dose, Two-treatment (Fed vs. Fasting), Two-period, Two-sequence, Crossover Study to Evaluate the Effects of Food on the Bioavailability of 60 mg ER Torsemide Tablet in Healthy Human Adult Subjects
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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