A Preliminary Study to Evaluate PF-07264660 in Healthy Participants

PHASE1CompletedINTERVENTIONAL
Enrollment

59

Participants

Timeline

Start Date

August 16, 2022

Primary Completion Date

May 6, 2024

Study Completion Date

May 6, 2024

Conditions
Healthy
Interventions
DRUG

PF-07264660 intravenous single ascending dose

PF-07264660 will be administered intravenously in single ascending doses

DRUG

PF-07264660 subcutaneous multiple ascending dose

PF-07264660 will be administered subcutaneously in multiple ascending doses

OTHER

Intravenous placebo

Placebo will be administered intravenously in single ascending doses

OTHER

subcutaneous placebo

Placebo will be administered subcutaneously in multiple ascending doses

Trial Locations (6)

53095

Spaulding Clinical Research, West Bend

55114

Prism Research LLC dba Nucleus Network, Saint Paul

78229

Clinical Trials of Texas, LLC, San Antonio

90720

Collaborative Neuroscience Research, LLC, Los Alamitos

90806

Collaborative Neuroscience Research, LLC, Long Beach

92845

Collaborative Neuroscience Research, LLC, Garden Grove

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY

NCT05496738 - A Preliminary Study to Evaluate PF-07264660 in Healthy Participants | Biotech Hunter | Biotech Hunter