Study Of PF-06817024 In Healthy Subjects, In Patients With Chronic Rhinosinusitis With Nasal Polyps And in Patients With Atopic Dermatitis

NCT02743871 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 97

Last updated 2022-05-19

Study results available
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Summary

The purpose of this study is to evaluate safety, tolerability, pharmacokinetics, and pharmacodynamics of PF-06817024 in healthy volunteers, in participants with chronic rhinosinusitis, with nasal polyps and in participants with moderate-to-severe Atopic Dermatitis

Conditions

Interventions

BIOLOGICAL

PF-06817024

Subjects will be given one dose of PF-06817024 intravenously

OTHER

Placebo for PF-06817024

Subjects will be given one dose of placebo for PF-06817024 intravenously

BIOLOGICAL

PF-06817024

Subjects will be given one dose of PF-06817024 subcutaneously

OTHER

Placebo for PF-06817024

Subjects will be given one dose of placebo for PF-06817024 subcutaneously

BIOLOGICAL

PF-06817024

Subjects will be given two doses of PF-06817024 intravenously

OTHER

Placebo for PF-06817024

Subjects will be given two doses of PF-06817024 intravenously

BIOLOGICAL

PF-06817024

Subjects will be given 2 doses intravenously

OTHER

Placebo for PF-06817024

Subjects will be given 2 doses intravenously

BIOLOGICAL

PF-06817024

Subjects will be given doses of PF-06817024 intravenously

OTHER

Placebo for PF-06817024

Subjects will be given doses of Placebo intravenously

Sponsors & Collaborators

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
SEQUENTIAL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-04-27
Primary Completion
2021-03-09
Completion
2021-03-09
FDA Drug
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02743871 on ClinicalTrials.gov