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Phase 2 Completed N=23 Treatment

Immunoadsorption, Dexamethasone Pulse Therapy and Rituximab for Pemphigus

Pemphigus
Source: ClinicalTrials.gov NCT00656656 ↗
Enrolled (actual)
23
Serious AEs
8.7%
Results posted
Dec 2016
Primary outcomePrimary: Number of Patients Achieving a Short- and Long-term Remission of Pemphigus — 23 Participants

Summary

Pemphigus is a severe autoimmune blistering disease mediated by circulating antibodies against certain proteins important for maintaining skin integrity. Protein A immunoadsorption is a dialysis-like technique selectively removing the antibodies from patient's blood. Rituximab is a synthetic antibody capable of destroying B cells. B cells are responsible for production of antibodies in the patients blood that, in turn, lead to clinical signs of pemphigus. Dexamethasone pulse therapy is a high-dose short-term corticosteroid therapy that may be used to suppress autoantibody production in pemphigus. While each of these three therapies had been used to treat pemphigus, none was shown effective in all cases. The hypothesis of this study is that a combination of protein A immunoadsorption, rituximab and dexamethasone is more effective that either of these treatments alone in achieving a rapid and durable improvement or cure in patients with pemphigus.

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Patients Achieving a Short- and Long-term Remission of Pemphigus
23
SECONDARY
Number of Patients Who Experienced Side-effects of Treatment
2

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of pemphigus confirmed by immunofluorescence and desmoglein ELISA.
  • Severe disease or past treatment(s) not effective or past treatment(s) not tolerated.

Exclusion Criteria

  • General condition too poor to tolerate immunoadsorption treatment.
  • Severe dementia or psychiatric disease.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00656656). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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