Actively Recruiting

Phase 3
Age: 18Years - 80Years
All Genders
NCT03295383

Randomized Clinical Trial Comparing the Safety and Efficacy of Rituximab Versus Oral Cyclophosphamide in Severe Forms of Mucous Membrane Pemphigoid

Led by University Hospital, Rouen · Updated on 2026-02-18

130

Participants Needed

27

Research Sites

398 weeks

Total Duration

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AI-Summary

What this Trial Is About

Mucous membrane pemphigoid (MMP) describes a group of chronic auto-immune bullous diseases (AIBD) of the basement membrane zone (BMZ), characterized by predominant or exclusive mucosal involvement, including oral, naso-pharyngeal, laryngo-tracheal, genital, oesophageal, anal and ocular mucous membranes. Circulating autoantibodies are directed against various antigens of the BMZ: BP180, laminin 332 and type 7 collagen. MMP is a rare disease with an incidence of 1.8 new cases/million inhabitants/year in France. Scar formation which is secondary to initial inflammation, is a characteristic feature of MMP, leading to major disability (e.g blindness and oesophageal, anal, vaginal stenosis) and life-threatening situations (e.g. laryngeal stenosis leading to respiratory failure). Dapsone is the first line treatment of mild/moderate forms of MMP. Dapsone is used both as initial treatment, and as maintenance therapy. However, severe forms of MMP can rapidly worsen leading to blindness, aphagia due to esophageal stenosis, respiratory failure due to tracheal or laryngeal stenosis, and urinary and sexual dysfunctions due to genital involvement. These patients are usually treated using immunosuppressive drugs. Indeed, corticosteroids (CS) are not recommended in MMP. Cyclophosphamide was considered as the most effective immunosuppressant in severe forms of MMP, before the use of rituximab, an anti-CD20 monoclonal antibody (MAb). Two series from our group have assessed the advantages and disadvantages of IV pulse and oral administration of cyclophosphamide in MMP. Oral administration seems more rapidly effective with 54% of complete remission (CR) after a median time of 24 weeks (16-52 weeks). The results of 41 patients with severe types of MMP (including a French series of 20 patients) treated with rituximab have been published. Rate of CR after one and two cycles were 66% and 90%, respectively. Clinical improvement was rapid, since a decrease in disease activity was observed after 4 weeks of treatment in 64% of patients. Our results and those of the literature suggest that rituximab might be more effective than cyclophosphamide, which has been considered as the gold standard of treatment in severe forms of disease, up to now.

CONDITIONS

Official Title

Randomized Clinical Trial Comparing the Safety and Efficacy of Rituximab Versus Oral Cyclophosphamide in Severe Forms of Mucous Membrane Pemphigoid

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female patients aged 18 to 80 years with newly or previously diagnosed severe mucous membrane pemphigoid
  • Clinical signs include blisters or erosions on mucous membranes with or without scarring
  • Skin involvement limited to no more than 2 of 4 bullous pemphigoid criteria
  • Linear deposits of IgG, IgA, and/or C3 on basement membrane zone by direct immunofluorescence
  • Subepithelial blister confirmed by histology when biopsy is possible
  • Severe MMP defined by sight-threatening ocular disease, life-threatening airway or esophageal stenosis, involvement of high-risk mucosal sites, multiple mucosal sites, or severe oral involvement
  • Disease not controlled despite at least one month of maximum tolerated dapsone treatment, or no prior dapsone treatment in severe cases
  • Patient has read and signed informed consent
  • Updated vaccinations as recommended
  • Women of childbearing potential agree to use adequate contraception or abstinence during treatment and for 12 months after
  • Men agree to abstinence or condom use during treatment and for 12 months after
  • Agreement to avoid excessive sunlight exposure during study
  • Ability to comply with study protocol as judged by investigator
  • Affiliated with or beneficiary of social security
Not Eligible

You will not qualify if you...

  • Age below 18 or above 80 years
  • Non-consenting or unable to be followed regularly
  • MMP sequelae without active inflammation
  • Brunsting Perry pemphigoid or exclusive skin lesions without mucosal involvement
  • Karnofsky performance status below 50%
  • Unstable angina or advanced ischemic heart disease within last 3 months
  • Severe heart failure (NYHA III/IV) or uncontrolled cardiac disease
  • Uncontrolled cardiac rhythm disorders
  • Severe bronchial obstruction
  • History of malignant disease within last 10 years or current progressive cancer except certain skin and cervical cancers
  • Anemia (Hb < 10 g/dL), neutropenia, lymphopenia, thrombocytopenia
  • Positive hepatitis B or C serology
  • Liver or major kidney insufficiency (creatinine clearance ≤ 30 ml/min)
  • Active or recent (within 24 weeks) alcohol or drug abuse
  • Positive HIV test
  • Severe immune deficiency
  • Active infections or recent infections requiring oral or IV antibiotics
  • History of severe infections within past year
  • Uncontrolled concomitant diseases that prevent participation
  • Use of oral or systemic corticosteroids within 12 weeks prior to randomization
  • Major surgery within 4 weeks before randomization
  • Immunosuppressive treatments or other active treatments for MMP within 4 weeks before baseline
  • Intravenous immunoglobulins or plasmapheresis within 8 weeks before randomization
  • Previous treatment with cyclophosphamide or rituximab
  • Previous B cell-targeted therapy other than rituximab
  • Live or attenuated vaccine within 28 days before randomization
  • Contraindications to study drugs or their excipients
  • Lactose intolerance
  • Lack of peripheral venous access
  • Pregnancy, lactation, or planning pregnancy within study and 12 months after
  • Participation in another interventional clinical trial within 28 days prior to randomization
  • Judicial or administrative restrictions such as guardianship or deprivation of liberty

AI-Screening

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Trial Site Locations

Total: 27 locations

1

CHU Amiens

Amiens, France

Actively Recruiting

2

CHU Angers

Angers, France

Actively Recruiting

3

CH Argenteuil

Argenteuil, France

Actively Recruiting

4

CHU Bordeaux

Bordeaux, France

Actively Recruiting

5

Brest University Hospital

Brest, France

Actively Recruiting

6

CHU Caen

Caen, France

Actively Recruiting

7

CHU Clermont Ferrand

Clermont-Ferrand, France

Actively Recruiting

8

CHU Dijon

Dijon, France

Actively Recruiting

9

CH Le Mans

Le Mans, France

Actively Recruiting

10

CHU Lille

Lille, France

Actively Recruiting

11

CHU de Limoges

Limoges, France

Actively Recruiting

12

HCL

Lyon, France

Actively Recruiting

13

APHM La Timone

Marseille, France

Actively Recruiting

14

CHU Montpellier

Montpellier, France

Actively Recruiting

15

CHU Nantes

Nantes, France

Actively Recruiting

16

CHU Nice

Nice, France

Actively Recruiting

17

APHP Avicennes

Paris, France

Actively Recruiting

18

APHP Bichat

Paris, France

Actively Recruiting

19

APHP Cochin

Paris, France

Actively Recruiting

20

APHP Henri Mondor

Paris, France

Actively Recruiting

21

APHP Pitié Salpétrière

Paris, France

Actively Recruiting

22

APHP Saint-Louis

Paris, France

Actively Recruiting

23

CH Quimper

Quimper, France

Actively Recruiting

24

CHU de Reims

Reims, France

Actively Recruiting

25

CHU Rennes

Rennes, France

Actively Recruiting

26

CHU saint-Etienne

Saint-Etienne, France

Actively Recruiting

27

CHU Tours

Tours, France

Actively Recruiting

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Research Team

P

Pascal JOLY, Pr

CONTACT

J

Julien BLOT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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