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NCT01945606

Study to Assess the Safety of BAY1067197 in Stable Heart Failure Patients on Standard Therapy Including ß-blocker

Completed Phase 2 Last updated 19 September 2019
What this trial tests

Phase 2 trial testing Placebo (treatment 1) in Heart Failure in 11 participants. Completed in 17 March 2015.

Timeline
29 November 2013
Primary endpoint
9 September 2014
17 March 2015

Quick facts

Lead sponsorBayer
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingsingle
Primary purposetreatment
Enrollment11
Start date29 November 2013
Primary completion9 September 2014
Estimated completion17 March 2015
Sites1 location across Netherlands

Drugs / interventions tested

Conditions studied

Sponsor

Bayer — full company profile →

Who can join

Adults 18 to 75, any sex, with Heart Failure. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a study to investigate the safety and tolerability of the partial A1 agonist BAY1067197 in patients with chronic heart failure. BAY1067197 will be applied as a single dose of 30 mg in addition to standard therapy including a beta-blocker. The aim of the study is to assess if a single oral dose of 30 mg BAY1067197 is well tolerated when given on top of standard therapy for heart failure, particularly ß-blocker treatment.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. The Adenosinergic System as a Therapeutic Target in the Vasculature: New Ligands and Challenges.
    Sousa JB, Diniz C. · · 2017 · cited 17× · PMID 28481238 · DOI 10.3390/molecules22050752

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Other recruiting trials for Heart Failure

Currently open trials in the same condition.

Other Bayer trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01945606.

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