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Safety, Tolerability and Pharmacokinetics of CSL112 in Healthy Volunteers

2014-08-27 03:13:27 | BioPortfolio

Summary

The purpose of this study is to assess the safety and tolerability of escalating doses of CSL112 after single intravenous infusions in healthy volunteers and to measure the pharmacokinetics of CSL112 after single intravenous infusions in healthy volunteers.

Study Design

Allocation: Randomized, Control: Placebo Control, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Conditions

Healthy

Intervention

CSL112 (reconstituted HDL), normal saline (0.9%)

Location

CMAX
Adelaide
South Australia
Australia
5000

Status

Recruiting

Source

CSL Limited

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:13:27-0400

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