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NCT02769702 · ClinicalTrials.gov registry record · Phase 4

Open Label Study of Acthar SQ Gel Injection in Patients With Active Anterior Uveitis

A Phase 4 study, sponsored by Washington University School of Medicine.

Terminated
Registry status
Phase 4
Development phase
2
Enrollment target

NCT02769702: Clinical Trial Phase 4 study, sponsored by Washington University School of Medicine.

NCT02769702 is a Phase 4 study that was terminated before completion, run by Washington University School of Medicine. The registered enrollment target is 2 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02769702, a Phase 4 study, was terminated before completion, sponsored by Washington University School of Medicine.

TERMINATED
Registry status
Phase 4
Development phase
2 participants
Enrollment target

Study Summary

Uveitis is an acute or chronic inflammatory condition of unknown etiology. Although uveitis often responds adequately to topical corticosteroids, there are many patients for which this treatment is either inadequate or not tolerated. A patient with inadequate response to treatment would manifest uveitis activity by slit lamp examination determination of anterior chamber cellularity. Lack of tolerance of therapy commonly manifests as ocular hypertension (greater than 21 mmHg measured by tonometry)complicating chronic topical corticosteroid administration, leading to glaucoma and permanent visual loss. Moreover, systemic corticosteroids may be required at a dose unsafe for chronic administration. In these situations, an immunosuppressive medication is often added as a "steroid-sparing" agent. If and when there is clinical response to the added immunosuppressive, the oral and/or topical corticosteroid dose can be reduced or eliminated to avoid toxicity. There are several reasons for believing that Acthar might be beneficial in the treatment of uveitis patients. In addition to increasing adrenal production or cortisol, Acthar has another important mechanisms of action mediated by its binding of melanocortin receptors. Melanocortin down-regulates activity of B and T lymphocytes, monocytes and macrophages. In animal studies, melanocortin peptides down-regulate T helper cells, up-regulate T Regulatory cells, and decrease B lymphocyte production of B Lymphocyte Stimulator. In macrophages, there is down-regulation of IL-1, IL-2, INF gamma, TNF alpha, nitric oxide and adhesion molecules. In other cells, in addition to IL-10 upregulation (monocytes), there is down-regulation of VACM and ECAM (endothelial cells), prostaglandins (fibroblasts) and MCP-1 and RANTES (renal tubules).CNS mediation of systemic inflammation may also be down-regulated by melanocortin receptor binding by Acthar.

Primary Outcome

standard assessment of uveitis activity. Scores were assessed using a Likert scale using 0 to 4, higher score reflects more cellularity.

Interventions

  • DRUG Acthar

Trial Details

FieldValue
Enrollment Target 2 participants
Start Date 2016-06
Est. Completion 2017-01-06
Phase Phase 4

Why NCT02769702 stopped before completion

NCT02769702 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 2 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (100% lower).

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

NCT02769702 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02769702 about?

NCT02769702 is a clinical study titled "Open Label Study of Acthar SQ Gel Injection in Patients With Active Anterior Uveitis". Uveitis is an acute or chronic inflammatory condition of unknown etiology. Although uveitis often responds adequately to topical corticosteroids, there are many patients for which this treatment is either inadequate or not tolerated. A patient with inadequate response to treatment would manifest uve...

What is the current status of trial NCT02769702?

This trial is currently terminated. It is a Phase 4 study. The enrollment target is 2 participants. The study started on 2016-06. Estimated completion is 2017-01-06.

What interventions are being tested in trial NCT02769702?

The interventions under investigation include: Acthar (DRUG).

Who is sponsoring clinical trial NCT02769702?

This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02769702's enrollment target sits among peer trials

2 1998th of 2000 higher than 1 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02769702, the US trial registry maintained by the National Library of Medicine. NCT02769702 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.