Evaluating Clinical and Immunological Effects of Rituximab With Cyclophosphamide Compared to Rituximab Alone in AAV Patients

Who is this study for? Patients with ANCA Associated Vasculitis
What treatments are being studied? Endoxan
Status: Recruiting
Location: See all (4) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

Most recent insights in the treatment for patients with ANCA-associated vasculitis (AAV) have demonstrated that 'tailored' maintenance treatment with rituximab (RTX) is effective to achieve durable remission of disease. As such, RTX re-treatment can be tailored on the basis of relevant clinical and immunological parameters in AAV patients. Now, the present study intends to evaluate whether combining rituximab with cyclophosphamide is superior to current standard of care with rituximab only to induce a favorable clinical and immunological state in AAV patients and can thereby reduce the number of tailored re-treatments with rituximab.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

⁃ Subjects enrolled in the study must meet the following inclusion criteria:

• Clinical diagnosis of granulomatosis with polyangiitis (GPA) or microscopic Polyangiitis (MPA), consistent with Chapel-Hill Consensus Conference definitions26

• Aged at least 18 years, with newly-diagnosed or relapsed AAV with 'generalised disease', defined as involvement of at least one major organ (e.g. kidney, lung, heart, peripheral or central nervous system), requiring induction treatment with cyclophosphamide or rituximab

• Positive test for anti-PR3 or anti-MPO (current or historic)

• Willing and able to give written Informed Consent and to comply with the requirements of the study protocol

Locations
Other Locations
Netherlands
Noordwest Ziekenhuisgroep
NOT_YET_RECRUITING
Alkmaar
Meander Medical Center
RECRUITING
Amersfoort
Leiden University Medical Center
RECRUITING
Leiden
HagaZiekenhuis
NOT_YET_RECRUITING
The Hague
Contact Information
Primary
YKO Teng, MD, PhD
y.k.o.teng@Lumc.nl
+31715262148
Time Frame
Start Date: 2019-05-03
Estimated Completion Date: 2025-04-01
Participants
Target number of participants: 100
Treatments
Active_comparator: Rituximab
Patients will be intravenously treated with Rituximab 1000mg (or biosimilar) in the first week and receive a 2nd dosage of 1000mg 14 days later. Before every infusion of Rituximab patients will receive intravenous methylprednisolone 100mg together with oral acetaminophen 1000 mg and and intravenous Tavegil 2 mg.
Active_comparator: Rituximab plus low-dose cyclophosphamide
5.1.2. Cyclophosphamide Patients will be intravenously treated with a total of 6 infusions of cyclophosphamide 500mg every 2 weeks. Before every infusion of cyclophosphamide patients will receive intravenous granisetron to prevent nausea.
Authors
S. McAdoo
Related Therapeutic Areas
Sponsors
Leads: Leiden University Medical Center

This content was sourced from clinicaltrials.gov