Tustin, California 92780

  • Heart Failure

Purpose:

This is a placebo-controlled study to determine the effect of CLP in heart failure subjects with fluid overload.


Criteria:

Selected Inclusion Criteria: - Age 21 years or older at randomization - Heart failure with at least one of the following signs of current fluid overload: 1. Peripheral (or sacral) edema >1+ or ascites during screening or on day of randomization 2. Pulmonary congestion as determined by chest X-ray during the screening period - Ambulatory and able to perform the 6-minute walk test Selected Exclusion Criteria: - Participation in another clinical trial of an investigational or marketed drug within 30 days or 5 half-lives (whichever is longer) preceding screening - Any hospitalization or unscheduled outpatient decongestion therapy using IV diuretics, ultrafiltration, or paracentesis within 8 weeks prior to or during screening - Coronary-artery bypass graft, percutaneous intervention (e.g., cardiac, cerebrovascular, aortic), or major surgery including thoracic and cardiac, within 2 months prior to or during screening or anticipated need during study participation - Heart transplant recipient, or anticipated need for transplant or LVAD during study participation - Any of the following events having occurred within 8 weeks prior to or during screening: myocardial infarction, transient ischemic attack, stroke, or acute coronary syndrome as judged by the Investigator


NCT ID:

NCT01736735


Primary Contact:

Study Chair
Howard Dittrich, MD
Sorbent Therapeutics, Study Sponsor

Jade Brennan
Phone: 919-491-5721
Email: jadebrennan@momentum-research.com


Backup Contact:

Email: jchang@sorbent.com
Jean Chang


Location Contact:

Tustin, California 92780
United States



There is no listed contact information for this specific location.

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: September 17, 2021

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