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NCT00283712 · ClinicalTrials.gov registry record · Phase 2

Use of Infliximab for the Treatment of Pemphigus Vulgaris

A Phase 2 study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

Completed
Registry status
Phase 2
Development phase
20
Enrollment target

NCT00283712: Completed Phase 2 study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

NCT00283712 is a Phase 2 study that has completed, run by National Institute of Allergy and Infectious Diseases (NIAID). The registered enrollment target is 20 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00283712, a Phase 2 study, has completed, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

COMPLETED
Registry status
Phase 2
Development phase
20 participants
Enrollment target

Study Summary

Pemphigus vulgaris (PV) is a rare skin disorder that causes blistering of the skin and mucous membranes. Infliximab is a man-made antibody used to treat certain types of immune system disorders, including rheumatoid arthritis and Crohn's disease. This study will determine if infliximab given in combination with prednisone is a safe and effective treatment for adults with PV.

Primary Outcome

Participants classified as responders at Week 18 had: 1. Achieved a prednisone dosage \<= 25% of the initial starting dose or \<= 10 mg/day (whichever is greater), and 2. Had no new blisters within the previous 4 weeks.

Interventions

  • DRUG Infliximab
  • OTHER Placebo Comparator

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2006-03
Est. Completion 2011-03
Phase Phase 2

What the finished NCT00283712 record still lists

NCT00283712 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower).

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

NCT00283712 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00283712 about?

NCT00283712 is a clinical study titled "Use of Infliximab for the Treatment of Pemphigus Vulgaris". Pemphigus vulgaris (PV) is a rare skin disorder that causes blistering of the skin and mucous membranes. Infliximab is a man-made antibody used to treat certain types of immune system disorders, including rheumatoid arthritis and Crohn's disease. This study will determine if infliximab given in comb...

What is the current status of trial NCT00283712?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 20 participants. The study started on 2006-03. Estimated completion is 2011-03.

What interventions are being tested in trial NCT00283712?

The interventions under investigation include: Infliximab (DRUG), Placebo Comparator (OTHER).

Who is sponsoring clinical trial NCT00283712?

This trial is sponsored by National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00283712's enrollment target sits among peer trials

20 1805th of 2000 higher than 107 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 NCT00283712, the US trial registry maintained by the National Library of Medicine. NCT00283712 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.