A study to learn how different amounts of the study medicine called PF-07941944 are tolerated in the body of healthy adults.

2024-515421-28-00 Protocol C5961001 Human pharmacology (Phase I) - First administration to humans Ended

Start 28 Nov 2024 · End 20 Jun 2025 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol C5961001

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - First administration to humans
Status Ended
Participants planned 66
Countries 1
Sites 1

RSV (Respiratory Syncytial Virus)

Key facts

Sponsor
Pfizer Inc.
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Diseases [C] - Virus Diseases [C02]
Trial duration
28 Nov 2024 → 20 Jun 2025
Decision date (initial)
2024-11-27
Transition trial
No
Low-intervention
No
Rare-disease indication
No
Vulnerable population
Yes

Trial design

CTIS Part I — objectives, methods, condition coding

Conditions and MedDRA coding

RSV (Respiratory Syncytial Virus)

VersionLevelCodeTermSystem organ class
21.1 PT 10061603 Respiratory syncytial virus infection 100000004862

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 66 1
Rest of world 0

Investigational sites

Belgium

1 site · Ended
Pfizer Clinical Research Unit
None, Route de Lennik 808, B-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 2024-11-28 2025-06-19 2024-12-03 2025-04-24

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2024-10-21 Belgium Acceptable
2024-11-27
2024-11-27