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NCT00356200 · ClinicalTrials.gov registry record · Phase 2

Fluphenazine Decanoate for Psoriasis

A Phase 2 study, sponsored by Tufts Medical Center.

Terminated
Registry status
Phase 2
Development phase
10
Enrollment target

NCT00356200: Clinical Trial Phase 2 study, sponsored by Tufts Medical Center.

NCT00356200 is a Phase 2 study that was terminated before completion, run by Tufts Medical Center. The registered enrollment target is 10 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00356200, a Phase 2 study, was terminated before completion, sponsored by Tufts Medical Center.

TERMINATED
Registry status
Phase 2
Development phase
10 participants
Enrollment target

Study Summary

We are doing this research study to evaluate the effectiveness and safety of fluphenazine decanoate when injected with a needle into psoriasis lesions in adults. Fluphenazine decanoate is FDA (U.S. Food and Drug Administration) approved for use in people who have schizophrenia and psychotic symptoms. Fluphenazine decanoate is not approved by the FDA for use in psoriasis. Fluphenazine decanoate slows T cell growth in cells in laboratory test tubes. Its usefulness and safety in people with psoriasis will be investigated in this study.

Primary Outcome

Change in score from 0-14 of target lesion disease activity based on scaling, erythema, and induration as determined by a physician assessor at week 4 compared to baseline (with 0 being no disease activity and 14 being maximum disease activity).

Interventions

  • DRUG Placebo
  • DRUG Fluphenazine Decanoate

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2006-07
Est. Completion 2008-09
Phase Phase 2
Tufts Medical Center

169 total trials

Why NCT00356200 stopped before completion

NCT00356200 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT00356200 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00356200 about?

NCT00356200 is a clinical study titled "Fluphenazine Decanoate for Psoriasis". We are doing this research study to evaluate the effectiveness and safety of fluphenazine decanoate when injected with a needle into psoriasis lesions in adults. Fluphenazine decanoate is FDA (U.S. Food and Drug Administration) approved for use in people who have schizophrenia and psychotic symptoms...

What is the current status of trial NCT00356200?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 10 participants. The study started on 2006-07. Estimated completion is 2008-09.

What interventions are being tested in trial NCT00356200?

The interventions under investigation include: Placebo (DRUG), Fluphenazine Decanoate (DRUG).

Who is sponsoring clinical trial NCT00356200?

This trial is sponsored by Tufts Medical Center, which has 169 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00356200's enrollment target sits among peer trials

10 1968th of 2000 higher than 12 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT00356200, the US trial registry maintained by the National Library of Medicine. NCT00356200 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.