A Single Ascending Dose Study Examining the Safety and Pharmacokinetic Profile of Reconstituted High Density Lipoprotein (CSL112) Administered to Patients: Difference between revisions
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To determine the safety, tolerability and pharmacokinetics of a single ascending dose of intravenous infusion of CSL-112 in patients with stable atherothrombotic disease. | To determine the safety, tolerability and pharmacokinetics of a single ascending dose of intravenous infusion of CSL-112 in patients with stable atherothrombotic disease. | ||
==Methods== | ==Methods== | ||
CSL-112 is a reconstituted formulation of apo A-1 derived from human plasma. This is a multi- | CSL-112 is a reconstituted formulation of apo A-1 derived from human plasma. This is a multi-centered, randomized, double-blinded, placebo-controlled, single ascending dose study where the treatment group gets intravenous CSL-112. | ||
==Results== | ==Results== | ||
Pending | Pending | ||
Revision as of 11:25, 18 September 2013
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A Single Ascending Dose Study Examining the Safety and Pharmacokinetic Profile of Reconstituted High Density Lipoprotein (CSL112) Administered to Patients On the Web |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Objective
To determine the safety, tolerability and pharmacokinetics of a single ascending dose of intravenous infusion of CSL-112 in patients with stable atherothrombotic disease.
Methods
CSL-112 is a reconstituted formulation of apo A-1 derived from human plasma. This is a multi-centered, randomized, double-blinded, placebo-controlled, single ascending dose study where the treatment group gets intravenous CSL-112.
Results
Pending