Multiple Oral Doses of BIBR 1048 MS Solution in Healthy Volunteers

NCT02170831 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2014-06-23

No results posted yet for this study

Summary

To assess safety, pharmacokinetics and the effect of BIBR 1048 MS on coagulation parameters.

Conditions

  • Healthy

Interventions

DRUG

BIBR 1048 MS low

DRUG

BIBR 1048 MS medium 1

DRUG

BIBR 1048 MS medium 2

DRUG

BIBR 1048 MS high

DRUG

BIBR 1048 MS placebo

Sponsors & Collaborators

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
1999-05-31
Primary Completion
1999-07-31

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02170831 on ClinicalTrials.gov