ADME: A Study to Understand What the Body does to the Study Compound Called PF-07220060 When Taken by Healthy Adults.

2023-507074-40-00 Protocol C4391010 Human pharmacology (Phase I) - Other Ended

Start 26 Jan 2024 · End 13 Apr 2024 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol C4391010

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Ended
Participants planned 12
Countries 1
Sites 1

metastatic/advanced breast cancer

Key facts

Sponsor
Pfizer Inc.
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male
Therapeutic area
Diseases [C] - Neoplasms [C04]
Trial duration
26 Jan 2024 → 13 Apr 2024
Decision date (initial)
2023-12-14
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

metastatic/advanced breast cancer

VersionLevelCodeTermSystem organ class
20.0 LLT 10027475 Metastatic breast cancer 10029104
21.1 LLT 10072737 Advanced breast cancer 10029104

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
Netherlands Ended 12 1
Rest of world 0

Investigational sites

Netherlands

1 site · Ended
Pharmaceutical Research Associates Group B.V.
Program Management, Van Swietenlaan 6, 9728 NZ, Groningen

Country notifications

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

Country Trial startTrial end Recruitment startRecruitment end Early termination
Netherlands 2024-01-26 2024-04-12 2024-01-31 2024-02-28

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2023-11-06 Netherlands Acceptable
2023-12-14
2023-12-14
2 SUBSTANTIAL MODIFICATION SM-1 2024-02-06 Netherlands Acceptable
2024-02-23
2024-02-27