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COMPLETED Phase 1

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

NCT00714116 · View on ClinicalTrials.gov ↗

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

769 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00714116

The ClinicalTrials.gov registry entry for NCT00714116 describes a study currently listed as completed. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer, which has 769 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00714116 reports 6 study locations spanning 4 distinct geographic areas — top geographies include Florida, North Carolina, Pennsylvania. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00714116?

The interventions under investigation include: SBI-087 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00714116?

This trial is sponsored by Pfizer, which has 769 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

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