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NCT00714116 · ClinicalTrials.gov registry record · Phase 1

Study Evaluating The SBI-087 In Subjects With Systemic Lupus Erythematosus

A Phase 1 study of Lupus Erythematosus, Systemic, sponsored by Pfizer.

Completed
Registry status
Phase 1
Development phase
30
Enrollment target
6
Study locations

NCT00714116 is a Phase 1 study of Lupus Erythematosus, Systemic that has completed, run by Pfizer. The registered enrollment target is 30 participants, below the 202-participant average among 29 other Lupus Erythematosus, Systemic trials with a reported enrollment target (85% lower). The trial reports 6 study locations across 4 states.

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The verdict

NCT00714116, a Phase 1 study of Lupus Erythematosus, Systemic, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 1
Development phase
30 participants
Enrollment target
6
Study locations

Study Summary

The purpose of this study is to determine the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of SBI-087 in subjects with Systemic Lupus Erythematosus (SLE).

Interventions

  • DRUG SBI-087

Study Locations (6)

Florida

  • Arthritis & Rheumatology Care Center - South Miami
  • Miami Research Associates - South Miami
  • MRA Clinical Research - South Miami

North Carolina

  • Duke University Medical Center - Durham

Pennsylvania

  • Altoona Center for Clinical Research - Duncansville

Texas

  • Metroplex Clinical Research Center - Dallas

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2009-03
Est. Completion 2012-09
Phase Phase 1

Sponsor

Pfizer

1,845 total trials

What the Registry Record Tells You About NCT00714116

The ClinicalTrials.gov registry entry for NCT00714116 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 202-participant average among 29 other Lupus Erythematosus, Systemic trials with a reported enrollment target (85% lower). The listed sponsor is Pfizer, which has 1,845 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Lupus Erythematosus, Systemic appearing as the primary indexed condition, and to 1 intervention - of which SBI-087 is the first listed.

NCT00714116 reports 6 study locations spanning 4 distinct geographic areas - top geographies include Florida, North Carolina, Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT00714116 about?

NCT00714116 is a clinical study titled "Study Evaluating The SBI-087 In Subjects With Systemic Lupus Erythematosus". The purpose of this study is to determine the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of SBI-087 in subjects with Systemic Lupus Erythematosus (SLE).

What is the current status of trial NCT00714116?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2009-03. Estimated completion is 2012-09.

What conditions does trial NCT00714116 study?

This clinical trial studies the following conditions: Lupus Erythematosus, Systemic.

What interventions are being tested in trial NCT00714116?

The interventions under investigation include: SBI-087 (DRUG).

Who is sponsoring clinical trial NCT00714116?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00714116 being conducted?

This trial has 6 study locations across Florida, North Carolina, Pennsylvania, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.