A Study to Learn How Different Amounts of the Study Medicine Called PF-07293893 are Tolerated and Act in the Body of Healthy Adults.

2023-508171-36-00 Protocol C5171002 Human pharmacology (Phase I) - Other Ended

Start 15 Dec 2023 · End 2 Dec 2024 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol C5171002

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Ended
Participants planned 108
Countries 1
Sites 1

heart failure with preserved ejection fraction

Key facts

Sponsor
Pfizer Inc.
Participant type
Healthy volunteers
Age range
18-64 years, 65+ years
Gender
Male and Female
Therapeutic area
Diseases [C] - Cardiovascular Diseases [C14]
Trial duration
15 Dec 2023 → 2 Dec 2024
Decision date (initial)
2023-12-13
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 with preserved ejection fraction

VersionLevelCodeTermSystem organ class
20.1 LLT 10076396 Heart failure with preserved ejection fraction 10007541

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Pfizer Inc.

Sponsor organisation
Pfizer Inc.
Address
66 Hudson Boulevard East
City
New York
Postcode
10001-2189
Country
United States

Scientific contact point

Organisation
Pfizer Inc.
Contact name
Clinical Medical Lead

Public contact point

Organisation
Pfizer Inc.
Contact name
Clinical Medical Lead

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Belgium Ended 48 1
Rest of world
United States
60

Investigational sites

Belgium

1 site · Ended
Pfizer Clinical Research Unit
N/A, Lennikse Baan 808, 1070, Brussels

Country notifications

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

Country Trial startTrial end Recruitment startRecruitment end Early termination
Belgium 2023-12-15 2024-08-27 2023-12-20 2024-07-10

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2023-11-07 Belgium Acceptable
2023-12-13
2023-12-13
2 SUBSTANTIAL MODIFICATION SM-1 2024-02-08 Belgium Acceptable
2024-02-26
2024-03-04
3 SUBSTANTIAL MODIFICATION SM-2 2024-04-22 Belgium Acceptable
2024-05-08
2024-05-16
4 NON SUBSTANTIAL MODIFICATION NSM-1 2024-05-17 Belgium Acceptable
2024-05-08
2024-05-17
5 SUBSTANTIAL MODIFICATION SM-3 2024-06-06 Belgium Acceptable
2024-06-18
2024-06-18