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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)

2014-08-27 03:15:55 | BioPortfolio

Summary

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.

Study Design

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

Conditions

Acute Heart Failure

Intervention

Cinaciguat (BAY58-2667), Cinaciguat (BAY58-2667), Placebo

Location

Cincinnati
Ohio
United States
45267-0542

Status

Recruiting

Source

Bayer

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:15:55-0400

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