Trial Profile

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: Active, no longer recruiting

Phase of Trial: Phase I

Latest Information Update: 09 Jul 2025

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At a glance

01 Jul 2025 Planned End Date changed from 31 Aug 2025 to 28 Aug 2025.
01 Jul 2025 Planned primary completion date changed from 31 Aug 2025 to 28 Aug 2025.
20 Apr 2025 Planned End Date changed from 30 Sep 2025 to 31 Aug 2025.

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