Skip to content

(21683) Phase 2b open-label clinical study to evaluate the tolerability and safety of an initiation dose of 5 mg of Vericiguat in participants with chronic heart failure with reduced ejection fraction

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-507682-25-00
Acronym
21683 "VELOCITY"
Enrollment
111
Registered
2024-05-08
Start date
2024-05-13
Completion date
2024-07-29
Last updated
2024-07-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic heart failure with reduced ejection fraction

Brief summary

Treatment tolerability, defined as the completion of the two-week 5 mg dose without discontinuation of study intervention, Treatment tolerability, defined as the completion of the two-week 5 mg dose without moderate to severe symptomatic hypotension between Visit 1 and Visit 2

Detailed description

Any AE reported between Visit 1 and 2, Absence of AE related to study intervention between Visit 1 and Visit 2., Continuous intake of study intervention between Visit 1 and Visit 2 or restart of study intervention after any temporary interruption.

Interventions

DRUGBAY 1021189

Sponsors

Bayer AG, Bayer AG
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Treatment tolerability, defined as the completion of the two-week 5 mg dose without discontinuation of study intervention, Treatment tolerability, defined as the completion of the two-week 5 mg dose without moderate to severe symptomatic hypotension between Visit 1 and Visit 2

Secondary

MeasureTime frame
Any AE reported between Visit 1 and 2, Absence of AE related to study intervention between Visit 1 and Visit 2., Continuous intake of study intervention between Visit 1 and Visit 2 or restart of study intervention after any temporary interruption.

Countries

Hungary, Italy, Poland, Spain, Sweden

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026