Skip to main content
OpenTrials
Completed

NCT Number: NCT01879020

Evaluation of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of TA-8995 After Multiple Doses in Healthy Subjects

The purpose of this study is to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of TA-8995 after multiple doses in healthy adult male subjects

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–55 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

Momentum Pharma Services GmbH

Hamburg, 22769, Germany

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Free from any clinically significant illness or disease as determined by their medical history, physical examination, laboratory and other tests and as judged by the Investigator.
  • Between 18 - 55 years old.
  • Male of Caucasian ethnic origin.
  • Body mass index (BMI) in the range of 19 - 33 kg/m² and had a minimum weight of 50 kg. Subjects with a BMI in the range 30.0 - 33.0 kg/m² had to have a waist measurement of ≤ 91 cm.

Exclusion criteria

  • High density lipoprotein (HDL)-C level of greater or equal to 2.59 mmol/L (≥ 100 mg/dL) at Screening.
  • Abnormal Electrocardiogram (ECG) at Screening or Day -1 including a QTc ≥ 430 ms (The QTc-interval was calculated automatically according to Bazett's formula. In the case of results of ≥ 430 ms, QTc was additionally calculated manually using Fridericia's formula which was used as an exclusion criterion).
  • Family history of long QT syndrome, hypokalaemia or Torsades de Pointes
  • Impaired endocrine, thyroid, hepatic, respiratory or renal function, diabetes mellitus, coronary heart disease or history of any psychotic illness
  • Presence or history of gastro-intestinal, hepatic or renal disease or any other condition known to interfere with the absorption, distribution, metabolism or excretion of drugs

Treatment and study plan

TA-8995

Drug

Drug: TA-8995 1mg

Placebo

Drug

Placebo (TA-8995 1mg)

Primary outcomes

  1. Number of participants with adverse events

    Time frame: 336 hours post dose

  2. Laboratory tests (haematology, biochemistry and urinalysis)

    Time frame: 336 hours post dose

  3. Vital signs (supine systolic and diastolic blood pressure, heart rate and body temperature)

    Time frame: 336 hours post dose

  4. Area under the plasma concentration (AUC) versus time curve over the final dosing interval (AUC0-τ, Steady-state)

    Time frame: 7 days post the final dose

  5. The last time point 't' with a concentration Ct ≥ Lower limit quantification (LLQ) (AUC0-t, Steady-state)

    Time frame: 7 days post the final dose

Secondary outcomes

  1. Cholesterol ester transfer protein (CETP) activity (%)

    Time frame: 7 days post the final dose

  2. CETP concentration (mg/mL)

    Time frame: 4 hours after the first and the fibal dose

Sponsors and collaborators

Lead sponsor

Tanabe Pharma Corporation

Industry

Registry information

Official study title

A Randomised Double-blind, Placebo-controlled, Ascending-dose, Phase I Study to Determine the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of TA-8995 After Multiple Doses in Healthy Adult Male Subjects

Important dates

Study start
2009
Primary completion
2010
Study completion
2010
First posted
Jun 17, 2013
Registry last updated
Jun 17, 2013

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.

Published trials that share one or more normalized conditions with this study.