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Monoclonal Antibodies
Sibeprenlimab for IgA Nephropathy
Phase 2 & 3
Waitlist Available
Research Sponsored by Otsuka Pharmaceutical Development & Commercialization, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing the safety and effectiveness of sibeprenlimab, an injectable medication, in patients with IgA Nephropathy who have been part of earlier studies. The medication likely helps manage symptoms or slow disease progression. Sibeprenlimab is being developed as a potential treatment for IgA nephropathy (IgAN).
Who is the study for?
This trial is for people with a kidney condition called IgA Nephropathy who have a certain level of kidney function (eGFR ≥ 20 mL/min/1.73 m2) and completed previous trials without safety issues. It's not open to those who didn't finish the earlier studies or developed conditions that would have excluded them.
What is being tested?
The study tests Sibeprenlimab, given as an injection under the skin every four weeks, to see how safe and effective it is over time for treating IgA Nephropathy.
What are the potential side effects?
While specific side effects are not listed here, participants will be monitored for any adverse reactions to Sibeprenlimab since assessing long-term safety and tolerability is one of the main goals of this phase.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Sibeprenlimab 400 mg s.c. q 4 weeksExperimental Treatment1 Intervention
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for IgA Nephropathy (IgAN) include angiotensin inhibition (e.g., enalapril, valsartan), which reduces proteinuria and protects kidney function by lowering blood pressure and decreasing glomerular pressure. Monoclonal antibodies like rituximab and sibeprenlimab target specific immune pathways, such as B-cell depletion or other immune modulators, to reduce inflammation and immune complex deposition in the kidneys.
Aliskiren, a direct renin inhibitor, also helps in reducing proteinuria. These treatments are crucial for IgAN patients as they address the underlying immune dysregulation and proteinuria, which are key factors in disease progression and kidney damage.
Rituximab In The Treatment Of Refractory Idiopathic Membranous Nephropathy In Pakistani Population.Successful Use of Aliskiren in a Case of IgA- Mesangial Glomerulonephritis Unresponsive to Conventional Therapies.Alemtuzumab Induction and Steroid Minimization in IgA Nephropathy: A Matched-Cohort Analysis.
Rituximab In The Treatment Of Refractory Idiopathic Membranous Nephropathy In Pakistani Population.Successful Use of Aliskiren in a Case of IgA- Mesangial Glomerulonephritis Unresponsive to Conventional Therapies.Alemtuzumab Induction and Steroid Minimization in IgA Nephropathy: A Matched-Cohort Analysis.
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Who is running the clinical trial?
Otsuka Pharmaceutical Development & Commercialization, Inc.Lead Sponsor
264 Previous Clinical Trials
169,479 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I completed a specific trial without safety issues and might benefit from sibeprenlimab.Your kidney function, as measured by eGFR, is at least 20 mL/min/1.73 m2.You developed a condition after participating in previous trials that would have kept you from joining this trial.
Research Study Groups:
This trial has the following groups:- Group 1: Sibeprenlimab 400 mg s.c. q 4 weeks
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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