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Completed Phase 1 Interventional Accepts healthy volunteers Results available

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

ClinicalTrials.gov ID: NCT02743871

Public ClinicalTrials.gov record NCT02743871. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 14, 2026, 10:14 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A PHASE 1, RANDOMIZED, DOUBLE-BLIND, THIRD-PARTY OPEN, PLACEBO-CONTROLLED, DOSE ESCALATING STUDY TO EVALUATE THE SAFETY, TOLERABILITY, PHARMACOKINETICS AND PHARMACODYNAMICS OF SINGLE AND/OR MULTIPLE INTRAVENOUS AND/OR SUBCUTANEOUS DOSES OF PF-06817024 IN HEALTHY SUBJECTS WHO MAY BE MILDLY ATOPIC, SUBJECTS WITH CHRONIC RHINOSINUSITIS WITH NASAL POLYPS, AND SUBJECTS WITH MODERATE-SEVERE ATOPIC DERMATITIS

Study identification

NCT ID
NCT02743871
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Pfizer
Industry
Enrollment
97 participants

Conditions and interventions

Interventions

  • PF-06817024 Biological
  • Placebo for PF-06817024 Other

Biological · Other

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 26, 2016
Primary completion
Mar 8, 2021
Completion
Mar 8, 2021
Last update posted
May 18, 2022

2016 – 2021

United States locations

U.S. sites
20
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
UC Davis Dermatology Sacramento California 95816
UC Davis CTSC Clinical Research Center Sacramento California 95817
UC Davis Health Sacramento California 95817
New Haven Clinical Research Unit New Haven Connecticut 06511
Dermatology Physicians of Connecticut Shelton Connecticut 06484
ForCare Clinical Research Tampa Florida 33613
Dawes Fretzin Clinical Research Group, LLC Indianapolis Indiana 46256
Dawes Fretzin Dermatology Group, LLC Indianapolis Indiana 46256
The Indiana Clinical Trials Center Plainfield Indiana 46168
Academic Dermatology Edina Minnesota 55435
Clinical Research Institute, Inc. Minneapolis Minnesota 55402
Ear, Nose & Throat Specialty Care of Minnesota, P.A. Minneapolis Minnesota 55404
Prism Research, LLC Saint Paul Minnesota 55114
Hassman Research Institute Berlin New Jersey 08009
Carolina Phase 1 Research, LLC Raleigh North Carolina 27612
Vital Prospects Clinical Research Institute, PC Tulsa Oklahoma 74136
Health Concepts Rapid City South Dakota 57702
Lee Medical Associates, PA San Antonio Texas 78213
Progressive Clinical Research, PA San Antonio Texas 78213
Virginia Clinical Research, Inc. Norfolk Virginia 23502

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02743871, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 18, 2022 · Synced May 14, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02743871 live on ClinicalTrials.gov.

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