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NCT02066311 · ClinicalTrials.gov registry record · Phase 2

Nelfinavir in Systemic Lupus Erythematosus

A Phase 2 study, sponsored by Northwell Health.

Terminated
Registry status
Phase 2
Development phase
15
Enrollment target

NCT02066311 is a Phase 2 study that was terminated before completion, run by Northwell Health. The registered enrollment target is 15 participants.

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The verdict

NCT02066311, a Phase 2 study, was terminated before completion, sponsored by Northwell Health.

TERMINATED
Registry status
Phase 2
Development phase
15 participants
Enrollment target

Study Summary

Systemic Lupus Erythematosus (SLE) is a chronic autoimmune disease in which the body's immune system attacks different parts of the body. SLE is characterized by inflammation that leads to tissue damage in different organ systems. Any organ system may be involved, including the skin, the joints, the kidneys, the nervous system, the heart, the lungs, and the blood. The exact cause of SLE is not known. Patients with SLE often have elevated levels of anti-double stranded DNA antibodies. These levels are often associated with disease flares and disease severity. These antibodies can bind to tissue leading to organ damage. Preventing these antibodies from binding to their targets may help decrease disease activity. Protease inhibitors are medications that have been approved by the Food and Drug Administration (FDA) for use in the treatment of HIV (human immunodeficiency virus). Nelfinavir (also called viracept) is one of these protease inhibitors. Separate from their anti-viral effects, protease inhibitors have been found to decrease inflammation. These medications have been shown to interfere with binding of anti-double stranded DNA antibodies to their targets and may decrease inflammation in SLE. This research study tests whether the protease inhibitor, nelfinavir, will decrease anti-double stranded DNA antibody binding and decrease disease activity.

Interventions

  • DRUG Nelfinavir

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2014-09
Est. Completion 2018-06
Phase Phase 2

Sponsor

Northwell Health

370 total trials

What the Registry Record Tells You About NCT02066311

The ClinicalTrials.gov registry entry for NCT02066311 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Northwell Health, which has 370 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Nelfinavir is the first listed.

NCT02066311 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02066311 about?

NCT02066311 is a clinical study titled "Nelfinavir in Systemic Lupus Erythematosus". Systemic Lupus Erythematosus (SLE) is a chronic autoimmune disease in which the body's immune system attacks different parts of the body. SLE is characterized by inflammation that leads to tissue damage in different organ systems. Any organ system may be involved, including the skin, the joints, the...

What is the current status of trial NCT02066311?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 15 participants. The study started on 2014-09. Estimated completion is 2018-06.

What interventions are being tested in trial NCT02066311?

The interventions under investigation include: Nelfinavir (DRUG).

Who is sponsoring clinical trial NCT02066311?

This trial is sponsored by Northwell Health, which has 370 total clinical trials registered on ClinicalTrials.gov.

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

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.