Efficacy of Rituximab in Comparison to Continued Corticosteroid Treatment in Idiopathic Nephrotic Syndrome

Focal Segmental Glomerulosclerosis Clinical Trial

Official title:

Efficacy of Rituximab in Comparison to Continued Corticosteroid Treatment in Idiopathic Nephrotic Syndrome Unresponsive to 8 Weeks of High Dose Prednisone

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03298698
• Other study ID #: RSRNS17
• Status: Recruiting
• Phase: Phase 3
• Start date: August 22, 2018
• Est. completion date: January 22, 2022

Study information

• Verified date: August 2018
• Source: Radboud University
• Contact: Jeroen Deegens, MD,PhD
• Phone: +31243614761
• Email: Jeroen.Deegens[@]radboudumc.nl
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This will be an open-label, randomized controlled trial which compares continued treatment with high dose prednisone (standard therapy) to treatment with rituximab in patients with minimal change disease or focal segmental glomerulosclerosis unresponsive to 8 weeks of high dose prednisone .

patients either receive 2 doses of Rituximab 375 mg/m2 iv at time 0 and 14 days with termination of prednisone or standard therapy which consist of 8 additional weeks of high dose prednisone treatment.

Description:

Minimal change disease (MCD) and focal segmental glomerulosclerosis (FSGS) are important causes of idiopathic nephrotic syndrome. First-line treatment with high dose prednisone up to 16 weeks is associated with serious side effects. Especially if treatment continues for more than 8 weeks.

Retrospective studies suggested that Rituximab may be more effective in patients unresponsive to 8 weeks of high dose prednisone. Treatment with rituximab was associated with a higher proportion of patients attaining remission of proteinuria and with fewer side effects.

This will be an open-label, randomized controlled trial which compares continued treatment with high dose prednisone (standard therapy) to treatment with rituximab in patients with an idiopathic nephrotic syndrome due to biopsy proven MCD or FSGS age 18 years or older.

All patients will be treated with high dose prednisone (1 mg/kg/day) for 8 weeks.

Patients can be included in the trial in case of persistent persistent proteinuria ≥ 2 g/ 24 hours or a protein-to-creatinine ratio ≥ 2 g/10mmol (2 g/g) after 8 weeks of treatment with high dose prednisone

Patients either receive 2 doses of Rituximab 375 mg/m2 iv at time 0 and 14 days with termination of prednisone or standard therapy which consist of 8 additional weeks of high dose prednisone treatment. In the Rituximab group, B-cells will be monitored weekly, and if no complete depletion is achieved, additional dose(s) of Rituximab will be given at a weekly interval (maximum of 2 additional doses) until complete B cell depletion.

Expected duration of the follow-up is 12 months, consisting of 9 visits.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 40
• Est. completion date: January 22, 2022
• Est. primary completion date: August 22, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age = 18 years

• Persistent proteinuria = 2 g/ 24 hours or a protein-to-creatinine ratio = 2 g/10mmol (2 g/g) after 8 weeks of treatment with high dose prednisone 1 mg/kg/day (max 80 mg/day)

• Idiopathic nephrotic syndrome caused by biopsy proven minimal change disease or focal segmental glomerulosclerosis

Exclusion Criteria:

• Severe nephrotic syndrome with hypotension

• Previous treatment with immunosuppressive medication other than prednisone

• Treatment with prednisone > 10 weeks in last six months

• Secondary form of FSGS or minimal change disease

• Patients who test positive for hepatitis B surface antigen (HBsAg) or hepatitis B core antibody (anti-HBc).

• Patients infected with HIV or suffering from other active infections

• Patients inoculated with a vaccine within 4 weeks prior to inclusion

• Pregnancy, breast feeding, women with inadequate contraception

• Malignancy

• Kidney transplantation

• Previous treatment with monoclonal antibodies within 2 years prior to inclusion

• Neutrophils < 1.5 x 109/L and/or platelet counts < 75 x 109/L

• Severe heart failure (New York Heart Association Class IV) or severe, uncontrolled cardiac disease

• Active peptic ulcer

• Known hypersensitivity to glucocorticoids

• Insulin resistant diabetes mellitus

• Treatment with carbamazepine, phenobarbital, phenytoin en rifampicin

• Severe osteoporosis with vertebral fracture

Related Conditions & MeSH terms

• Focal Segmental Glomerulosclerosis
• Glomerulosclerosis, Focal Segmental
• Idiopathic Nephrotic Syndrome
• Minimal Change Disease
• Nephrosis
• Nephrosis, Lipoid
• Nephrotic Syndrome
• Syndrome

Intervention

Drug:
• Rituximab
Rituximab: 375 mg/m2 intravenously on day 0 and day 14 B-cells will be monitored weekly, and if no complete depletion is achieved, additional dose(s) of Rituximab will be given at a weekly interval until complete B cell depletion (maximum of 2 additional doses).
• Prednisone
Prednisone 1 mg/kg/day (max 80 mg/day) for 8 weeks

Locations

Country	Name	City	State
Netherlands	Radboud University Medical Center	Nijmegen

Sponsors (1)

Lead Sponsor	Collaborator
Radboud University

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Complete remission	The proportion of patients reaching complete remission defined as proteinuria <0.3 g/day or < 300 mg/g	8 weeks
Secondary	Partial remission	The proportion of patients reaching partial remission defined as proteinuria < 3.5 g/24 h or < 3.5 g/g and 50% lower than baseline proteinuria	8 weeks
Secondary	Late complete or partial remission	The proportion of patients reaching complete remission defined as proteinuria <0.3 g/day or < 300 mg/g or The proportion of patients reaching partial remission defined as proteinuria < 3.5 g/24 h or < 3500 mg/g and 50% lower than baseline proteinuria	2-12 months
Secondary	Time to remission	Time between start of treatment and reaching partial or complete remission	12 months
Secondary	Time to relapse	The time between partial or complete remission and relapse (defined as urinary protein excretion to =3.5 g/24 h or =3.5 g/g creatinine	12 months
Secondary	Proportion of patients with a relapse	The proportion of patients with relapse (defined as urinary protein excretion to =3.5 g/24 h or =3.5 g/g creatinine in patients who had at least attained a partial remission and the time to relapse	12 months
Secondary	Proportion of patients treated with additional immunosuppressive drugs	Proportion of patients treated with immunosuppressive drugs other than the assigned treatment with rituximab or prednisolone	12 months
Secondary	General health assessment	Difference in general health measured by RAND-36	at 2, 6, 9 and 12 months
Secondary	Quality of life measured with TAAQOL	Difference in quality of life measured with TNO-academisch Ziekenhuis Leiden Questionnaire for Adult's Health-Difference in Quality of Life	at 2, 6, 9 and 12 months
Secondary	Proportion of patients with adverse events	The proportion of patients with adverse events. Adverse events graded according to Common Terminology Criteria For Adverse Events (NCI-CTCAE v4.03)	at 2 and 12 months
Secondary	Cost-effectiveness analysis	Cost-effectiveness will be calculated by dividing the difference in costs by the difference in effectiveness (based on the number of patients in remission) derived from the two groups. The resulting cost-effectiveness ratio will be expressed as costs per one more patient in remission	at 2, 6, 9 and 12 months
Secondary	Cost-utility analysis	Cost-utility analysis will be calculated by dividing the difference in costs by the difference in Quality Adjusted Life Years (QALY's). QALY's will be derived from the EuroQol-5d-5L questionnaire.	at 2, 6, 9 and 12 months
Secondary	Difference in kidney function	Difference in creatinine clearance and estimated glomerular filtration rate	at 2 and 12 months
Secondary	Proportion of patients with an increase of baseline serum creatinine = 50%	The percentage of patients with an increase > 50% of serum creatinine from baseline.	at 2 and 12 months
Secondary	Benefit-risk ratio 1	Difference in the percentage of remissions (benefit) divided by the difference in adverse events grade 3 or 4, including Serious Adverse Events and Suspected Unexpected Serious Adverse Reaction (risk)	at 2 and 12 months
Secondary	Benefit-risk ratio 2	Difference in the percentage of remissions (benefit) divided by the difference in the total number of adverse events (risk)	at 2 and 12 months