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Completed

NCT Number: NCT02531568

Drug Interaction Study of Warfarin and MT-3995

The purpose of this study is to evaluate the effects of MT-3995 on the PK of warfarin

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Key information

Conditions

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Clinical research organization

Neu-Ulm, Wegenerstraße, Germany

About this study

The purpose of this study is to evaluate the potential effects of multiple once daily doses of MT-3995 on the PK of (S)-warfarin and (R)-warfarin after single-dose administration of racemic warfarin

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Able and willing to provide written informed consent to participate in this study
  • Healthy, free from clinically significant illness or disease
  • White Caucasian male or female, aged 18 to 55 years
  • Body weight ranging from 50 (females) and 60 (males) to110 kg (inclusive)
  • Must have coagulation test results (including international normalised ratio [INR] and activated partial thromboplastin time [aPTT]) within the laboratory reference range at Screening.

Exclusion criteria

  • Presence or history of serious adverse reaction or allergy to any medicinal product
  • Known contraindication or adverse reaction to warfarin.
  • Presence of Cytochrome P450 2C9 (CYP2C9) and Vitamin K epoxide reductase complex subunit 1 (VKORC1) genetic polymorphisms that are known to increase warfarin sensitivity at Screening.
  • Known contraindications to heparin administration.
  • Known contraindication to parenteral vitamin K administration.

Treatment and study plan

Warfarin

Drug

MT-3995

Drug

Primary outcomes

  1. Cmax of warfarin with MT-3995 versus warfarin alone

    Time frame: 8 days

  2. AUC of warfarin with MT-3995 versus warfarin alone

    Time frame: 8 days

Secondary outcomes

  1. International normalized ratio (INR) max of warfarin with MT-3995 versus warfarin alone

    Time frame: 8 days

  2. INR AUC of warfarin with MT-3995 versus warfarin alone

    Time frame: 8 days

Sponsors and collaborators

Lead sponsor

Tanabe Pharma Corporation

Industry

Registry information

Official study title

A Phase I, Open-label, Single-Centre, Drug-Drug Interaction Study to Evaluate the Influence of MT-3995 on Pharmacokinetics(PK) and Pharmacodynamics of Warfarin in Healthy Subjects

Important dates

Study start
2015
Primary completion
2015
Study completion
2015
First posted
Aug 24, 2015
Registry last updated
Oct 9, 2015

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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