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Terminated Phase 1 Interventional

A Multiple Dose Study Of PD-0360324 In Patients With Active Cutaneous Lupus Erythematosus

ClinicalTrials.gov ID: NCT01470313

Public ClinicalTrials.gov record NCT01470313. 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 Jul 22, 2026, 9:14 AM 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 Randomized, Subject And Investigator-Blinded (Sponsor-Open), Placebo-Controlled Study To Evaluate The Safety, Tolerability, And Preliminary Efficacy Of Multiple Ascending Doses Of PD- 0360324 In Subjects With Active Cutaneous Lupus Erythematosus (CLE)

Study identification

NCT ID
NCT01470313
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
Pfizer
Industry
Enrollment
28 participants

Conditions and interventions

Interventions

  • PD-0360324 Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
21 Years to 70 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Oct 31, 2011
Primary completion
Oct 31, 2013
Completion
Oct 31, 2013
Last update posted
Jan 28, 2014

2011 – 2013

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
Pfizer Investigational Site Anniston Alabama 36207
Pfizer Investigational Site Oxford Alabama 36203
Pfizer Investigational Site Los Angeles California 90045
Pfizer Investigational Site Orange Park Florida 32073
Pfizer Investigational Site Chicago Illinois 60611
Pfizer Investigational Site Indianapolis Indiana 46256
Pfizer Investigational Site Fort Gratiot Michigan 48059
Pfizer Investigational Site Charlotte North Carolina 28210
Pfizer Investigational Site Ducansville Pennsylvania 16635
Pfizer Investigational Site Philadelphia Pennsylvania 19107
Pfizer Investigational Site Wyomissing Pennsylvania 19610
Pfizer Investigational Site Rapid City South Dakota 57701
Pfizer Investigational Site Rapid City South Dakota 57702
Pfizer Investigational Site Jackson Tennessee 38305
Pfizer Investigational Site Dallas Texas 75246
Pfizer Investigational Site Norfolk Virginia 23507
Pfizer Investigational Site Clarksburg West Virginia 26301

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01470313, 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 Jan 28, 2014 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01470313 live on ClinicalTrials.gov.

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