Effect of Huaier Granule on the Treatment of Idiopathic Membranous Nephropathy

Nephropathy Clinical Trial

Official title:

Effect of Huaier Granule on the Treatment of Idiopathic Membranous Nephropathy: a Multicenter, Randomized, Open-label, Parallel Controlled Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05839314
• Other study ID #: HE-202009
• Status: Recruiting
• Phase: Phase 4
• Start date: May 9, 2023
• Est. completion date: July 1, 2027

Study information

• Verified date: June 2024
• Source: Chinese PLA General Hospital
• Contact: Xiangmei Chen, PhD
• Phone: 00-86-010-66937166
• Email: shengdai26[@]163.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a prospective, multicenter, randomized, open-label, parallel controlled study. The purpose of this study is to evaluate the efficacy and safety of Huaier granule on the treatment of idiopathic membranous nephropathy comparing with Ciclosporin soft capsules.

Description:

Idiopathic membranous nephropathy (IMN) is a common immune-mediated glomerular disease, accounting for 20% to 36.8% of adult nephrotic syndrome. A third of the patients will experience complete remission spontaneously, and 30%-40% of patients will develop chronic renal failure. The treatment of IMN includes supportive therapy and immunosuppressive therapy. Ciclosporin (CsA) is a kind of calcineurin inhibitor (CNI) recommended by the Kidney disease improving global outcomes (KDIGO) clinical practice guideline for IMN treatment. CsA is effective in inducing remission among patients with steroid-resistant nephrotic IMN, and studies showed the clinical remission rate was 60%-75%. However, it has a high rate of relapse during follow-up in 6-12 months.

Huaier granule is an extract from a medicinal fungus. Previous studies showed that Huaier granule reduced the excretion of proteinuria, inhibited inflammation and cellular transdifferentiation, and protect renal function.

In this study, about 30 research centers will participate. We plan to enroll 480 participants (240 cases in the experimental group and 240 cases in the control group). The planned length of patient recruitment enrolment will be 2 years and the total length of visits be 1 year.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 480
• Est. completion date: July 1, 2027
• Est. primary completion date: May 3, 2027
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Renal biopsy was performed before randomization and pathologically diagnosed as idiopathic membranous nephropathy;

• Anti-phospholipase a2 receptor (PLA2R) antibody is positive;

• Aged from 18 to 75, either sex;

• Tolerable doses of RASI were received for =4 weeks before randomization, nephrotic syndrome was not in remission and 24-hour urinary protein level was =3.5g/24h and < 8.0g/24h;

• The eGFR=45ml/min/1.73m2 (Measured at least twice in 2 weeks);

• The patient is willing to sign the informed consent form.

Exclusion Criteria:

• Diagnosed as secondary membranous nephropathy;

• Rapidly progressive membranous nephropathy (eGFR decreased by 50 % compared with the baseline level within 3 months);

• Receiving renal replacement therapy;

• Diabetes and glycosylated hemoglobin (HbA1c) levels = 7.0%;

• Hypertension is not well controlled (systolic blood pressure>160mmHg or diastolic blood pressure>100mmHg);

• The level of serum albumin=20g/L;

• Resistance to treatment with CsA or other CNI, rituximab (RTX) or alkylating agents; complete remission or partial remission was obtained after treatment with CNI, RTX, or alkylating agents but there was a history of relapse within 3 months;

• Suspected infection by imaging and/or laboratory tests;

• Infectious diseases, such as hepatitis B, hepatitis C, AIDS, tuberculosis;

• History of malignant tumor;

• Hepatic dysfunction: aspartate aminotransferase (AST) concentration and alanine aminotransferase (ALT) concentration of > 1.5 × upper limit of normal;

• Allergic to Huaier granule or Ciclosporin soft capsules;

• Previous CNI treatment was ineffective;

• Complicate with any diseases that may affect efficacy and safety evaluation;

• Pregnant or lactating women, and patients (male or female) with fertility plans or unwilling to take effective contraceptive measures;

• Participating in other clinical trials or participated in other clinical studies within 3 months;

• According to the researchers, patients have diseases or conditions that increase the difficulty of enrollment or probability of loss to follow-up, such as mental illness, frequent changes in residence and work, etc.

Related Conditions & MeSH terms

• Glomerular Diseases
• Glomerulonephritis, Membranous
• Idiopathic Membranous Nephropathy
• Kidney Diseases
• Nephropathy

Intervention

Drug:
• Huaier granule
Huaier granule, oral administration, 10g each time, 3 times a day, continuous medication for 24 weeks. After 24 weeks of treatment, the dosage should be adjusted according to efficacy.
• Renin-angiotensin-aldosterone system inhibitors (RASI)
Run-in period: All the patients should be treated with RASI for at least 4 weeks, and stop using any medicine containing Huaier or similar ingredients for at least 2 weeks before enrollment. If the patient is receiving RASI, the RASI can be continued until the end of the study. RASI can be adjusted once a week until the maximum tolerable dose based on albuminuria and blood pressure. If the patient is not receiving RASI therapy, then RASI is recommended. Treatment period: RASI therapy is continued throughout the trial. Check blood pressure twice daily: morning and evening.
• Ciclosporin soft capsules
The initial dose of Ciclosporin soft capsules is an oral dose of 3.5mg/kg/d, divided into two equal doses, given every 12 hours. Assess the plasma concentration of CsA (valley value) every 2 weeks in the first 8 weeks. If the plasma concentration of CsA reaches 100-150ug/L, continue to maintain the dose. If the plasma concentration of CsA is below the target concentration, increase the dose of CsA. If the plasma concentration of CsA is higher than the upper limit of the target concentration, appropriate dose reduction. A single dose adjustment is 25mg/d. After increasing/decreasing the dose, CsA concentration is remeasured at intervals of 2 weeks ±3 days until the target concentration is reached. CsA at target concentration followed by 24 weeks of treatment, then the dosage shall be adjusted according to efficacy.

Locations

Country	Name	City	State
China	Chinese PLA general hospital	Beijing	Beijing

Sponsors (3)

Lead Sponsor	Collaborator
Chinese PLA General Hospital	Huazhong University of Science and Technology, LinkDoc Technology (Beijing) Co. Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall clinical remission rate at 24, 48, 96 weeks	Overall clinical remission rate is defined as rate of complete remission and partial remission. Complete remission is defined as a 24-h urinary protein level < 0.3g/d with normal serum albumin level and stable renal function. Partial remission is defined as 24-h urinary protein level < 3.5g/d with peak value reduction = 50%, accompanied by improved or normal serum albumin, stable renal function.	Start of randomization until 96 weeks
Secondary	Rate of complete remission at 24, 48, 96 weeks	The rate of patients achieve complete remission at 24, 48, or 96 weeks.	Start of randomization until 96 weeks
Secondary	Rate of partial remission at 24, 48, 96 weeks	The rate of patients achieve partial remission at 24, 48, or 96 weeks.	Start of randomization until 96 weeks
Secondary	Median time to achieve complete remission		Start of randomization until 96 weeks
Secondary	Median time to achieve partial remission		Start of randomization until 96 weeks
Secondary	Median time of the first relapse of nephrotic syndrome for patients who achieve complete remission or partial remission		Start of randomization until 96 weeks
Secondary	Proportion of patients with relapse of nephrotic syndrome		Start of randomization until 96 weeks
Secondary	Rate of treatment failure at the end of the study	Treatment failure: the efficacy has not reached complete or partial remission	Start of randomization until 96 weeks
Secondary	The proportion of reappearance proteinuria (but not reach nephrotic syndrome) for patients with complete response		Start of randomization until 96 weeks
Secondary	The 24-hour urinary protein level and changes from baseline at 24, 48, 96 weeks		Start of randomization until 96 weeks
Secondary	The serum albumin level and changes from baseline at 24, 48, 96 weeks		Start of randomization until 96 weeks
Secondary	Changes of serum creatinine at 24, 48, 96 weeks		Start of randomization until 96 weeks
Secondary	Changes of blood urea nitrogen at 24, 48, 96 weeks		Start of randomization until 96 weeks
Secondary	Changes of serum uric acid at 24, 48, 96 weeks		Start of randomization until 96 weeks
Secondary	Changes of serum blood lipid level at 24, 48, 96 week		Start of randomization until 96 weeks
Secondary	The level and changes of estimated glomerular filtration rate (eGFR) calculating using the CKD-EPI formula at 24, 48, 96 weeks		Start of randomization until 96 weeks
Secondary	Percentage of patients who serum creatinine doubled for 12 weeks, progress to end-stage renal disease, or receive renal replacement therapy		Start of randomization until 96 weeks
Secondary	The number and proportion of patients who died for any reason		Start of randomization until 96 weeks
Secondary	The level of phospholipase A2 receptor (PLA2R) and changes from baseline at 24, 48, 96 weeks		Start of randomization until 96 weeks
Secondary	The level and changes of immunoglobulin and complement		Start of randomization until 96 weeks
Secondary	Incidence and severity of adverse events (AE) and serious adverse events (SAE)		Start of randomization until 96 weeks
Secondary	Incidence and severity of adverse reactions (ADR), serious adverse reactions (SADR)		Start of randomization until 96 weeks