Clinical Trials Directory

Trials / Completed

CompletedNCT06712082

A Study to Learn More About the Study Medicine PF-07264660 in Healthy Chinese Adult Participants

A Phase 1, Randomized, Double-Blind, Third-Party Open, Placebo-Controlled, Single-Dose Study to Evaluate the Pharmacokinetics, Safety, Tolerability, Immunogenicity, and Pharmacodynamics Following Intravenous Dose of PF-07264660 in Chinese Healthy Adult Participants

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
12 (actual)
Sponsor
Pfizer · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to learn if the study medicine (called PF-07264660) is safe and how it is processed in healthy Chinese participants. This study is seeking participants who: * are between 18 to 65 years of age. * are Chinese participants who are overtly healthy as determined by medical evaluation. * have a BMI (body mass index) of 19 to 28 kilogram per meter squared; and a total body weight of more than50 kilograms (110 pounds). All participants in this study will receive study medicine. Three-fourths will receive PF-07264660 and one-fourth will receive placebo. A placebo does not have any medicine in it but looks just like the medicine being studied. The study medicine will be given as an IV infusion (directly into a vein) at the study clinic only one time. The study will compare the experiences of people receiving PF-07264660 to those of people who do not. This will help see if PF-07264660 is safe and how it behaves inside the human body. Participants will take part in this study for up to 181 days. During this time, the participants will stay at the study clinic for 5 days. After the stay, the participants will have 8 study visits at the study clinic.

Conditions

Interventions

TypeNameDescription
DRUGPF-07264660PF-07264660 solution for injection (single use only)
OTHERPlaceboPlacebo solution for injection (single use only)

Timeline

Start date
2025-02-24
Primary completion
2025-09-04
Completion
2025-09-04
First posted
2024-12-02
Last updated
2025-09-25

Locations

2 sites across 1 country: China

Regulatory

Source: ClinicalTrials.gov record NCT06712082. Inclusion in this directory is not an endorsement.