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A placebo controlled, double-blind and randomized study to assess different doses of a new drug (BAY58-2667) given intravenously, to evaluate if it is safe and can help to improve the well-being of patients with acute decompensated heart failure.
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Cinaciguat (BAY58-2667), Cinaciguat (BAY58-2667), Cinaciguat (BAY58-2667), Placebo
Published on BioPortfolio: 2014-08-27T03:16:07-0400
A Phase IIb Study to Investigate the Efficacy and Tolerability of Low Dose Cinaciguat (25 µg/h, 10 µg/h) Given Intravenously to Subjects With Acute Decompensated Chronic Congestive Heart Failure (ADHF)
A placebo controlled, double-blind and randomized study to assess different doses of a new drug (BAY58-2667) given intravenously, to evaluate if it is safe and can help to improve the well...
The purpose of this study is to assess a dose titration scheme, of a new drug (BAY 58-2667) given intravenously, to evaluate if this is safe and can help to improve the well-being, symptom...
The high volume of flowback water (FW) generated during shale gas exploitation is highly saline, and contains complex organics, iron, heavy metals, and sulfate, thereby posing a significant challenge ...
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