Vericiguat (BAY1021189)
DrugA : 2.5 mg vericiguat A*: 2.5 mg vericiguat B : 5 mg vericiguat C : 10 mg vericiguat C*: 10 mg vericiguat
NCT Number: NCT03504982
The primary objective of this study was to investigate whether there is a clinically meaningful effect on QTc change from baseline relative to placebo after administration of 10 mg at steady state in patients with stable CAD (coronary artery disease).
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Notify Me30 year–80 year
All sexes
Interventional
Phase 1
Universitätsherzzentrum Freiburg - Bad Krozingen, Bad Krozingen, Baden-Wurttemberg, Germany
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
A : 2.5 mg vericiguat A*: 2.5 mg vericiguat B : 5 mg vericiguat C : 10 mg vericiguat C*: 10 mg vericiguat
D: 400 mg moxifloxacin
A : vericiguat placebo 10 mg A*: vericiguat placebo 10 mg + moxifloxacin placebo B : vericiguat placebo 10 mg C : vericiguat placebo 2.5 mg C*: vericiguat placebo 2.5 mg + moxifloxacin placebo D : vericiguat placebo 2.5 mg + vericiguat placebo 10 mg
Time frame: Baseline, day 56 (steady state 10 mg) of vericiguat treatment
Time frame: Baseline and day 1 of vericiguat treatment
Time frame: Baseline and day 15 (+/- 3 days) of vericiguat treatment
Time frame: Baseline and day 29 (+/- 3 days) of vericiguat treatment
Time frame: Baseline and day 14 (+/- 3 days) of vericiguat treatment (steady state 2.5 mg)
Time frame: Baseline and day 28 (+/- 3 days) of vericiguat treatment (steady state 5 mg)
Time frame: Baseline and day 8 of the moxifloxacin treatment period
Time frame: On profile day 1; Timeframe: 0 - 5 hours after dosing
Time frame: On profile day 1; Timeframe: 0 - 5 hours after dosing
Time frame: On profile days: 8, 14, 15, 28, 29, 42, 43, 50 and 56; Timeframe: 0 - 5 hours after dosing
Time frame: On profile days: 1, 8, 14, 15, 28, 29, 42, 43, 50 and 56; Timeframe: 0 - 5 hours after dosing
Time frame: On moxifloxacin profile days (day 8 and 50); Timeframe: 0 - 5 hours after dosing
Time frame: On moxifloxacin profile days (day 8 and 50); Timeframe: 0 - 5 hours after dosing
Time frame: 12 months
Bayer
Industry
Study to Clinically Evaluate the QT/QTc Interval Prolongation Potential of Vericiguat in Patients With Stable Coronary Artery Disease in a 2-arm, Placebo-controlled, Randomized, Double-blind, Double-dummy Design Including a Vericiguat Multiple-dose Part With Fixed up Titration Periods and Moxifloxacin as Positive Control (for Assay Sensitivity Testing, Nested Into the Placebo Treatment)
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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