Efficacy of Dapsone as a Steroid Sparing Agent in Pemphigus Vulgaris

Stopped early · Phase 2

Conditions studied: Pemphigus Vulgaris

In brief

The purpose of this 12-month study was to determine the efficacy of dapsone as a glucocorticoid-sparing agent in maintenance phase pemphigus vulgaris.

Key facts

Study ID

NCT00429533

Run by

Jacobus Pharmaceutical

People needed

48

Starts

1996-11-01

Expected to finish

2004-02-01

Last updated by the study team

2007-02-05

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Histologic evidence compatible with pemphigus vulgaris and direct immunofluorescence evidence of pemphigus vulgaris.
• Chronic disease that has been controlled with steroids and/or cytotoxics, e.g. maintenance phase.
• On prednisone 15 or more mg/day to around 40 mg/day or on prednisone 15 or more mg every other day (qod) to around 40 mg qod.
• Failure to taper steroids below a range of 15 mg/day to around 40 mg/day or 15 mg/qod to around 40 qod without flaring the disease.
• The steroid dosage at which the most recent flare occurred should not be less than 85% of the last (within 30 days) dosage which controlled the disease, i.e. 85% of the baseline steroid dosage. This is to ensure that patients will not have had a recent acute flare at the time of entry into the study, and be in the rapid steroid taper portion of their disease after such a flare.
• Two baseline steroid dosages as determined by prior flares. It is common that patients will be repetitively unable to taper below a certain baseline steroid dose without experiencing a mild flare of their disease. This baseline dose will be determined on two occasions during attempted tapers, and the baseline number then averaged to determine the dose of steroid the patient is on at the time of entry into the study.
• No pulse steroids, pulse cyclosphosphamide, or plasmapheresis within two months of beginning the protocol. This will exclude patients who had recent acute flares of their disease and may be on the rapid steroid taper portion of their disease. The patient must be in maintenance phase, as defined in the criteria listed in e.
• Patient understands the procedures and agrees to participate in the study program by giving written informed consent.

You may not qualify if…

• Patients able to taper steroids without recurrence of disease.
• Patients with early, severe disease that have not responded to high doses of prednisone, cytotoxics, plasmapheresis, or other modalities.
• Contraindications to the use of Dapsone, including severe anemia or G6PD deficiency.
• Patient has behavioral problems that might interfere with compliance.
• Pregnancy or breast-feeding.
• Younger than 18 or older than 80 years of age. Since PV is rare in patients younger than 18, it was decided to exclude this potentially different population. It is unlikely that this will exclude many patients. Dapsone induces a hemolytic anemia, which would be a particular problem for patients over age 80, who are more likely to have ischemic heart disease or other atherosclerotic vascular disease.
• History of allergy to dapsone.
• Ischemic heart disease

Where it is running

• Northwestern University Medical Center — Chicago, Illinois, United States
• Rush-Presbyterian-St. Luke's Medical Center — Chicago, Illinois, United States
• Henry Ford Hospital — Detroit, Michigan, United States
• Cooper Hospital/University Medical Center — Camden, New Jersey, United States
• The New York VA Medical Center, New York University — New York, New York, United States
• Case Western Reserve University School of Medicine — Cleveland, Ohio, United States
• University of Pennsylvania — Philadelphia, Pennsylvania, United States
• University of Texas — Dallas, Texas, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.