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Pilot Study of Rituximab Therapy for Systemic Lupus Erythematosus (SLE) and Vasculitis

Primary Purpose

Systemic Lupus Erythematosus, ANCA Associated Vasculitis

Status
Completed
Phase
Phase 2
Locations
United Kingdom
Study Type
Interventional
Intervention
Rituximab
Sponsored by
Cambridge University Hospitals NHS Foundation Trust
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Systemic Lupus Erythematosus focused on measuring Rituximab, ANCA, vasculitis, lupus,

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Diagnosis of SLE or ANCA associated vasculitis Active disease refractory to 6 months conventional therapy with cyclophosphamide, prednisolone and at least one other immunosupressive agent ( or a lesser period if this therapy cannot be tolerated) Age 18-70 Exclusion Criteria: HbeAg or HCV Ab positive or known HIV positivity ( HIV testing not necessary for this study) Pregnancy, inadequate contraception or lactation Malignancy Current enrolment in pother clinicla trials -

Sites / Locations

  • Addenbrooke's Hospital

Outcomes

Primary Outcome Measures

1. Clinical remission at 6 or 12 months
2. Absence of a severe life threatening adverse event

Secondary Outcome Measures

Full Information

First Posted
February 16, 2006
Last Updated
February 16, 2006
Sponsor
Cambridge University Hospitals NHS Foundation Trust
Collaborators
Roche Pharma AG
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1. Study Identification

Unique Protocol Identification Number
NCT00293072
Brief Title
Pilot Study of Rituximab Therapy for Systemic Lupus Erythematosus (SLE) and Vasculitis
Official Title
Pilot Study of Rituximab Therapy for Systemic Lupus Erythematosus (SLE) and Vasculitis Resistant to Conventional Therapy
Study Type
Interventional

2. Study Status

Record Verification Date
October 2005
Overall Recruitment Status
Completed
Study Start Date
March 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
May 2005 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Cambridge University Hospitals NHS Foundation Trust
Collaborators
Roche Pharma AG

4. Oversight

5. Study Description

Brief Summary
Lupus and vasculitis are autoimmune conditions which can be life threatening. In order to treat these conditions toxic therapies such as cyclophosphamide and steroids are often required. These standard treatments are associated with significant side effects. Furthermore a proportion of patient do not respond to these conventional therapies. Newer safer therapies are being sought. Rituximab is a drug that eliminates B cell from the blood. B cells are one part of the human immune system that helps prevent infections. Abnormal activity of the immune system is responsible for autoimmune disease although the exact mechanisms in lupus and vasculitis are not yet established. Rituximab is liscenced as a treatment for a form of B cell cancer called non-Hodgkins Lymphoma and has a good safety track record when used in this context. It has recently been used to treat some autoimmune conditions with positive results. In this pilot study we wish to assess the effectiveness and safety of rituximab in patients with lupus and vascultis that are resistant to conventional therpies.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Systemic Lupus Erythematosus, ANCA Associated Vasculitis
Keywords
Rituximab, ANCA, vasculitis, lupus,

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
20 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Rituximab
Primary Outcome Measure Information:
Title
1. Clinical remission at 6 or 12 months
Title
2. Absence of a severe life threatening adverse event

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of SLE or ANCA associated vasculitis Active disease refractory to 6 months conventional therapy with cyclophosphamide, prednisolone and at least one other immunosupressive agent ( or a lesser period if this therapy cannot be tolerated) Age 18-70 Exclusion Criteria: HbeAg or HCV Ab positive or known HIV positivity ( HIV testing not necessary for this study) Pregnancy, inadequate contraception or lactation Malignancy Current enrolment in pother clinicla trials -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ken Smith
Organizational Affiliation
Cambridge Institute for Medical Research, Addenbrooke's Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
David Jayne
Organizational Affiliation
Lupus and Vasculitis Service, Addenbrooke's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Addenbrooke's Hospital
City
Cambridge
State/Province
Cambridgeshire
ZIP/Postal Code
CB2 2QQ
Country
United Kingdom

12. IPD Sharing Statement

Learn more about this trial

Pilot Study of Rituximab Therapy for Systemic Lupus Erythematosus (SLE) and Vasculitis

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