Skip to main content
OpenTrials
Completed

NCT Number: NCT04448821

A Clinical Trial to Evaluate the Effect of Nilotinib on the PK/PD of Meformin

The aim of the study is to evaluate the effect of nilotinib on the pharmacokinetics and pharmacodynamics of metformin in healthy male adults

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

19 year–50 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

Korea University Guro Hospital

Seoul, Guro-gu, 08308, South Korea

About this study

Pharmacokinetics and pharmacodynamics of metformin without coadministration of nilotinib will be compared with those after administration of nilotinib.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Healthy male subjects between the ages of 19 and 50 years
  • Subjects with body mass index (BMI) between 18.5 and 29.9 kg/m2 and weight more than 50 kg
  • Subjects who agree with performing contraception during the study
  • Subjects who provides written informed consent

Exclusion criteria

  • Subjects who have a current or prior history of cardiovascular, respiratory, hepatic, renal, hematological, gastrointestinal, endocrine, immunologic, skin, psychiatric, or neurological diseases that is clinically significant
  • Subjects who have clinically significant allergic history or allergy to metformin, nilotinib, or other components of drug
  • Subjects with history of galactose intolerance, lapp lactase deficiency, or glucose-galactose malabsorption
  • Subjects with hypokalemia or hypomagnesemia at screening
  • Subjects with QTcF > 450 or clinically significant findings on 12-lead ECG at screening
  • Subjects with fasting plasma glucose lower than 70 mg/dL or upper than 126 mg/dL at screening
  • Subjects who have history of gastrointestinal surgery
  • Subjects with creatinine clearance ≤ 60mL/min at screening
  • Subjects with AST or ALT ≥ 2-folds of upper normal limit
  • Subjects who reports less than 12 points on taste test at screening
  • Subjects who have administrated drugs that are known to cause significant drug-drug interaction with investigational drugs within 2 weeks prior to dosing
  • Whole blood donation within 60 days prior to dosing, or apheresis donation within 20 days prior to dosing, or received blood donation within 30 days prior to dosing
  • Subjects who participated in a previous clinical trial within 6 months prior to dosing
  • Subjects with a history of alcohol abuse
  • Subjects who are determined as unsuitable for clinical trial participation by investigator's decision

Treatment and study plan

metformin

Drug

Single administration of metformin

Metformin + Nilotinib

Drug

Coadministration of metformin and nilotinib

Primary outcomes

  1. Cmax

    Time frame: 24 hours post-dose

    maximum concentration

  2. AUCinf

    Time frame: 24 hours post-dose

    Area under the concentration-time curve from time of administration extrapolated to infinity

  3. Gmax

    Time frame: 3 hours from 2 hour post-dose

    maximum glucose level during oral glucose tolerance test

  4. AUGC

    Time frame: 3 hours from 2 hour post-dose

    Area under the concentration-time curve during oral glucose tolerance test

Secondary outcomes

  1. Taste test

    Time frame: 7 hour post-dose

Sponsors and collaborators

Lead sponsor

Hyewon Chung

Other

Registry information

Official study title

A Clinical Trial to Evaluate the Effect of Nilotinib on the Pharmacokinetics and Pharmacodynamics of Metformin in Healthy Male Adults

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Jun 26, 2020
Registry last updated
Nov 4, 2020

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.