A study to learn about the taste of Vericiguat given in liquid form in healthy male participants aged 18 to 45 years

2023-508447-52-00 Protocol 22342 Human pharmacology (Phase I) - Other Ended

Start 28 Jun 2024 · End 30 Sep 2024 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol 22342

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Ended
Participants planned 20
Countries 1
Sites 1

Heart failure in children

Key facts

Sponsor
Bayer AG
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male
Therapeutic area
Diseases [C] - Cardiovascular Diseases [C14]
Trial duration
28 Jun 2024 → 30 Sep 2024
Decision date (initial)
2024-06-04
Transition trial
No
Low-intervention
No
Rare-disease indication
No
Vulnerable population
No

Trial design

CTIS Part I — objectives, methods, condition coding

Conditions and MedDRA coding

Heart failure in children

VersionLevelCodeTermSystem organ class
20.0 LLT 10019279 Heart failure 10007541

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Bayer AG

Sponsor organisation
Bayer AG
Address
Kaiser-Wilhelm-Allee 1, Wiesdorf Wiesdorf
City
Leverkusen
Postcode
51373
Country
Germany

Scientific contact point

Organisation
Bayer AG
Contact name
Therapeutic Area Head

Public contact point

Organisation
Bayer AG
Contact name
Therapeutic Area Head

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Germany Ended 20 1
Rest of world 0

Investigational sites

Germany

1 site · Ended
CRS Clinical Research Services Management GmbH
Clinical Investigator, Grenadierstrasse 1, Neckarstadt, Mannheim

Country notifications

Trial-start, recruitment-start, end and early-termination notifications submitted per Member State

Country Trial startTrial end Recruitment startRecruitment end Early termination
Germany 2024-06-28 2024-09-30 2024-07-01 2024-08-20

Application history

1 submissions — initial application plus substantial / non-substantial modifications

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2024-03-22 Germany Acceptable
2024-05-17
2024-06-04