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The efficacy of rituximab for recalcitrant Pemphigus Vulgaris in the patients of Razi hospital from 2007 to 2011

The efficacy of rituximab for recalcitrant Pemphigus Vulgaris in the reduction of prednisolone dose

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201111022704N2
Enrollment
40
Registered
2011-12-03
Start date
2007-03-21
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pemphigus vulgaris. Pemphigus vulgaris

Interventions

rituximab 500 mg intravenously weekly for 4 weeks in each cycle.
Treatment - Drugs
rituximab 500 mg intravenously weekly for 4 weeks in each cycle

Sponsors

Vice-chancellor for Research of Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients with Pemphigus Vulgaris who are candidates for rituximab (failure to respond or frequent recurrences under long-term (months to years) oral corticosteroids more than 10 mg daily with or without additional immunosuppressive therapy? or oral corticosteroids intolerance with or without short and long-term oral coricosteroids side effects) Exclusion criterion were: pregnancy and breast feeding?history of sensitization to murine protein?hepatitis B cariers?cardiac arrhythmias & angina pectoris?high tumor burden?active infections

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Therapeutic effect(new blisters per day, Nikolsky’s sign and epithelialization over the denuded surfaces). Timepoint: weekly for 1 month and then monthly after injecting rituximab. Method of measurement: clinical examination.;The dose of oral prednisolone. Timepoint: prior to treatment, next 3 months, next 6 months and the final in the last visit. Method of measurement: mg per day.

Secondary

MeasureTime frame
Side effects. Timepoint: weekly for 1 month and then monthly after injecting rituximab. Method of measurement: clinical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSomayeh Khezri

Tehran University of Medical Sciences

khezri@razi.tums.ac.ir+98 21 5560 9951

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026