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Clinical Trial Summary

This is a Phase 1, randomized, double-blind, third-party open (ie, participant-blind, investigator-blind and sponsor-open), placebo-controlled, dose escalating clinical study to evaluate the safety, tolerability, immunogenicity, PK and PD of PF-06480605 in Japanese healthy adult participants.


Clinical Trial Description

Approximately 16 participants are planned to be enrolled into the study. The study consists of 2 cohorts, and approximately 6 participants will be randomized to PF-06480605 and approximately 2 participants will be randomized to placebo in each cohort. Each participant will receive PF-06480605 or placebo subcutaneously. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04269538
Study type Interventional
Source Telavant, Inc.
Contact
Status Completed
Phase Phase 1
Start date February 19, 2020
Completion date November 11, 2020

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