Study Completed

Prevention of venous thromboembolism after MOS

Bayer Identifier:

12362

ClinicalTrials.gov Identifier:

Not Available

EudraCT Number:

2009-012008-14

EU CT Number:

Not Available

BAY59-7939,Dose proportionality II for SPAF

Trial purpose

Please see attached Study Results Summary below

Key Participants Requirements

Sex

N/A

Age

18 - 45 Years

Trial summary

Enrollment Goal

Trial Dates

July 2009 - August 2009

Phase

Phase 1

Could I Receive a placebo

N/A

Products

Xarelto (Rivaroxaban, BAY59-7939)

Accepts Healthy Volunteer

N/A

Where to participate

Status	Institution	Location
Completed	CRS Clinical-Research-Services Mannheim GmbH	Mannheim, 68167, Germany

Trial design

Randomized, non-blind, non-controlled, 3-way crossover study to assess the pharmacokinetics, safety and tolerability of different dose strengths of rivaroxaban administered with food in healthy male subjects

Trial Type

Interventional

Intervention Type

N/A

Trial Purpose

N/A

Allocation

N/A

Blinding

N/A

Assignment

N/A

Trial Arms

N/A

Additional Information

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