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First in Man Clinical Study to Investigate Safety, Tolerability and Pharmacokinetics of Single Ascending Doses of CM3.1-AC100

2014-08-27 03:17:25 | BioPortfolio

Summary

A first time in man, phase I study to assess the safety, tolerability and pharmacokinetics of single ascending doses of CM3.1-AC100 in healthy male volunteers.

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Basic Science

Conditions

Healthy

Intervention

CM3.1-AC100, Placebo

Location

Parexel International GmbH
Berlin
Germany
14050

Status

Completed

Source

CellMed AG, A Subsidiary of Biocompatibles International plc.

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:17:25-0400

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