Published in Vaccine Weekly, February 28th, 2007
The study was a double-blind, placebo-controlled clinical trial conducted with 72 participants with mild to moderate hypertension. It was designed to evaluate safety, tolerability, and exploratory efficacy of two dose levels of the vaccine . For efficacy evaluation, the change in blood pressure from baseline to post-treatment was assessed in individual subjects by 24-hour ambulatory blood pressure monitoring.
Treatment with CYT006-AngQb was safe and very well tolerated. The majority of...
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Source: Vaccine Weekly (2007-02-28)
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