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OpenTrials
Completed

NCT Number: NCT01014416

Pharmacokinetics/Pharmacodynamics (PK/PD) Characteristics of Tolvaptan Tablet in Korean Healthy Male

To investigate the safety, tolerance, pharmacokinetics and pharmacodynamics of tolvaptan 15, 30 and 60 mg after single oral administration in healthy Korean male subjects.

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Key information

Conditions

Age range

20 year–45 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

Seoul National University Hospital

Seoul, South Korea

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Healthy Korean male subjects between 20 and 45 years of age, inclusive.
  • Body Mass Index (BMI) of 20 to 26 kg/m2, body,weight ≥ 50kg BMI = weight (kg)/height2(m)
  • Informed consent from the subjects

Exclusion criteria

  • Clinically significant abnormality of respiratory, cardiovascular, hepatic, neurologic, endocrine, hematologic, urinary, psychiatric.
  • History of gastrointestinal disease or surgery which can affect intestinal absorption of the study drug.
  • History of any significant drug allergy or hypersensitivity.
  • AST or ALT > 1.25 times upper normal limit at screening clinical laboratory test
  • Supine blood pressure after resting for ≥ 3 minutes, higher than 140/90 mmHg or lower than 100/50 mmHg, Supine pulse, after resting for ≥ 3 minutes, outside the range of 40 to 90 beats/minute.
  • Subjects who had history of drug abuse or alcohol addiction
  • Subjects who used of any prescription drug or herbal medication within 2 weeks prior to the first dosing of the study drug, or any over-the-counter or vitamin supplements within 1 week prior to the first dosing (However, investigators can judge the subject, who has taken the medications during those periods above, eligible for the trial if all other conditions are satisfied)
  • The investigator judges the subject not eligible for the study after reviewing clinical laboratory results or other reasons.

Treatment and study plan

Tolvaptan 15mg or 30mg or 60mg or Placebo

Drug

Single dose of Tolvaptan 15mg or 30mg or 60mg or Placebo per day

Primary outcomes

  1. PK parameters: AUC, Cmax, Tmax

    Time frame: 1 day

  2. PD parameters: 24 hour fluid balance

    Time frame: 1 day

  3. Safety: adverse event, body weight, physical examination, vital sign, ECG, clinical laboratory test

    Time frame: 4 days

Sponsors and collaborators

Lead sponsor

Korea Otsuka Pharmaceutical Co., Ltd.

Industry

Registry information

Official study title

A Dose Block-randomized, Double-blind, Placebo-controlled, Single Dose, Dose-escalation Study to Investigate the Safety, Tolerance, Pharmacokinetics and Pharmacodynamics of Tolvaptan in Healthy Korean Male Subjects Bipolar Disorder

Important dates

Study start
2010
Primary completion
2010
Study completion
2010
First posted
Nov 17, 2009
Registry last updated
Mar 11, 2010

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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