Data from Clinicaltrials.gov - Curated by EPG Health - Last updated 22 June 2017

The primary objective is to test the hypothesis that, compared with placebo, therapy with Subcutaneous (SQ) GLP-1 agonist in the post-Acute Heart Failure Syndrome (AHFS) discharge period...

purpose

The primary objective is to test the hypothesis that, compared with placebo, therapy with Subcutaneous (SQ) GLP-1 agonist in the post-Acute Heart Failure Syndrome (AHFS) discharge period will be associated with greater clinical stability at six months as assessed by a composite clinical endpoint.

Category Value
Study type(s) Interventional
Expected enrolment 300
Study start date 01-Apr-13
Estimated primary completion date 01-Oct-15

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