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Completed

NCT Number: NCT03215875

A Food Effect Study of 60mg ER Torsemide

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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Key information

Age range

18 year–45 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

I.E.C. Consultants

Bangalore, 560003, India

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • healthy male or female
  • non-smoker
  • weight ≥ 50 kg for male and ≥ 45 for female
  • clinically acceptable laboratory profiles with ECG and chest x-ray performed within 6 months

Exclusion criteria

  • participation in bioavailability/bioequivalence studies in past six months
  • history of drug abuse or alcohol dependence
  • history of allergies, known hypersensitivity to Torsemide and related drugs
  • presence of clinically significant disorder
  • suffer from high/low blood pressure (<90 and >140 mm Hg)
  • positive urine drug screening, and
  • history of incontinence

Treatment and study plan

Fed- 60mg ER Torsemide

Drug

60mg ER Torsemide will be given after high fat, high-calorie meal

Other names: High fat/high-calorie fed conditions

Fasting- 60mg ER Torsemide

Drug

60mg ER Torsemide will be given after overnight fasting

Other names: Fasting conditions

Primary outcomes

  1. Peak torsemide plasma concentration

    Time frame: 36 hours

    Peak plasma concentration (Cmax) (ng/ml) in fed and fasting conditions

  2. Total torsemide plasma concentration

    Time frame: 36 hours

    Area under the plasma concentration versus time curve (AUC) (hr/ng/ml) in fed and fasting conditions

Secondary outcomes

  1. Urinary torsemide excretion

    Time frame: 36 hours

    torsemide will be measured in urine over 36 hours post-dose (microgram/min)

  2. Urinary sodium excretion

    Time frame: 36 hours

    36-hour sodium excretion will be measure (mmol/min)

Sponsors and collaborators

Lead sponsor

Sarfez Pharmaceuticals, Inc.

Industry

Registry information

Official study title

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

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Jul 12, 2017
Registry last updated
Apr 18, 2018

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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