A Study to Learn How Different Amounts of the Study Medicine Called PF-07985631 are Tolerated and Act in the Body in Healthy Adults

2024-519215-33-00 Protocol C5661001 Human pharmacology (Phase I) - First administration to humans Ongoing, recruitment ended

Start 7 Aug 2025 · Status Ongoing, recruitment ended · 1 EU/EEA countries · 1 sites · Protocol C5661001

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - First administration to humans
Status Ongoing, recruitment ended
Participants planned 92
Countries 1
Sites 1

IgA nephropathy

Key facts

Sponsor
Pfizer Inc.
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Diseases [C] - Immune System Diseases [C20]
Trial duration
7 Aug 2025 → ongoing
Decision date (initial)
2025-07-01
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

IgA nephropathy

VersionLevelCodeTermSystem organ class
28.0 PT 10021263 IgA nephropathy 100000004857

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 Ongoing, recruitment ended 92 1
Rest of world 0

Investigational sites

Belgium

1 site · Ongoing, recruitment ended
Pfizer Clinical Research Unit
N/A, 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 2025-08-07 2025-08-13 2026-03-09

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2025-05-15 Belgium Acceptable with conditions
2025-07-01
2025-07-01
2 SUBSTANTIAL MODIFICATION SM-1 2025-07-11 Belgium Acceptable
2025-07-30
2025-07-30
3 NON SUBSTANTIAL MODIFICATION NSM-2 2025-07-31 Belgium Acceptable
2025-07-30
2025-07-31
4 SUBSTANTIAL MODIFICATION SM-2 2025-09-09 Belgium Acceptable
2025-09-25
2025-09-25