Status:
COMPLETED
A Study to Investigate the Effect of YM150 on the Plasma Concentration of Digoxin in Healthy Subjects
Lead Sponsor:
Astellas Pharma Inc
Conditions:
Healthy
Pharmacokinetic of Digoxin
Eligibility:
All Genders
18-55 years
Phase:
PHASE1
Brief Summary
This study is to evaluate the effect of YM150 on the plasma concentration of digoxin in healthy subjects.
Detailed Description
The study will be of a double blind, randomized, two period crossover design. Two treatments, digoxin in combination with YM150, and digoxin in combination with placebo, will be evaluated. Each subjec...
Eligibility Criteria
Inclusion
- Healthy, as judged by the investigator or sub-investigator based on the results of physical examinations and all tests
- Body weight: male: ≥60 kg, \<100 kg; female: ≥45.0 kg, \<80.0 kg
- BMI (at screening): ≥18.0, \<30.0
Exclusion
- Female subjects of child-bearing potential, not practicing adequate methods to prevent pregnancies, like abstinence or double barrier methods
- Known or suspected hypersensitivity / allergy to FXa inhibitors, digoxin, or heart glycosides in general or the constituents of the formulations used
- History of and/or any sign or symptom indicating current abnormal hemostasis or blood dyscrasia, including but not limited to neutropenia, thrombocytopenia, thrombocytopathy, thromboasthenia, hemophilia, Von Willebrand's disease, and vascular purpura, bleeding gums, or frequent nose bleeding
- Family history of congenital vascular malformation (e.g. Marfan's Syndrome) and/or bleeding disorder (e.g. hemophilia, Von Willebrand's disease, Christmas disease)
- PT or aPTT at the screening visit outside the normal range
- History of peptic ulcer or of any other organic lesion susceptible to bleed
- Any surgical intervention (including tooth extraction) or trauma within the last 3 months preceding the initiation of the study
- Any clinically significant history of upper gastrointestinal symptoms (such as nausea, vomiting, abdominal discomfort or upset, or heartburn) in the 4 weeks prior to admission to the Research Unit
- Any clinically significant history of any other disease or disorder - gastrointestinal, cardiovascular, respiratory, renal, hepatic, neurological, dermatological, psychiatric or metabolic
- Any of the liver function tests (ALAT, ASAT, LDH and γ-GT) above the upper limit of normal range (ULN)
- Any clinically significant abnormality following the investigator's review of the prestudy physical examination, ECG and clinical laboratory tests
- Abnormal pulse rate and blood pressure measurements at the pre-study visit as follows: Pulse rate \<40 or \>90 bpm; systolic blood pressure \<95 or \>160 mmHg; diastolic blood pressure \<40 or \>95 mmHg (measurements taken after subject has been resting in supine position for 5 min)
- Regular use of any prescribed or OTC (over-the-counter) drugs (including natural and herbal remedies and especially those with P-gp inhibiting activity, like St. John's worth) in the four weeks prior to admission to the Research Unit OR any use of such drugs (including natural and herbal remedies) as well as vitamins in the two weeks prior to admission to the Research Unit
- Donation of blood or blood products within 3 months prior to admission to the Research Unit
Key Trial Info
Start Date :
February 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 1 2006
Estimated Enrollment :
24 Patients enrolled
Trial Details
Trial ID
NCT01514812
Start Date
February 1 2006
End Date
April 1 2006
Last Update
January 24 2012
Active Locations (1)
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1
Paris, France