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Phase 1 Dosing Study of BAX 513 in Healthy Volunteers

2014-08-27 03:16:08 | BioPortfolio

Summary

The purpose of the study is to investigate whether orally administered BAX 513 (different doses administered for 5 days) affects hemostatic parameters in healthy volunteers.

Study Design

Allocation: Randomized, Control: Placebo Control, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Basic Science

Conditions

Not Applicable (Healthy Volunteers)

Intervention

Fucoidan (extract of Laminaria japonica), Placebo

Location

University Clinic for Clinical Pharmacology, General Hospital Vienna
Vienna
Austria
1090

Status

Recruiting

Source

Baxter Healthcare Corporation

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:16:08-0400

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