18 Participants Needed

Ravulizumab for IgA Nephropathy

Recruiting at 10 trial locations
Age: < 65
Sex: Any
Trial Phase: Phase 3
Sponsor: Alexion Pharmaceuticals, Inc.
Must be taking: RASI
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Pivotal Trial (Near Approval)This treatment is in the last trial phase before FDA approval
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a medicine called ravulizumab for children and teens with IgA nephropathy, a kidney disease that can cause protein to leak into the urine. The goal is to understand how the medicine works in young people compared to adults. Participants receive the medicine through an IV (a tube into a vein) on specific days, with dosing frequency based on their weight. Children and teens with this kidney issue who meet certain health requirements might be suitable for this study. As a Phase 3 trial, this study represents the final step before FDA approval, offering participants a chance to contribute to the potential availability of a new treatment.

Will I have to stop taking my current medications?

The trial requires that participants stay on a stable dose of RASI (ACEI and/or ARB) for at least 3 months before and during the study. If you are on these medications, you will need to continue taking them without changes.

Is there any evidence suggesting that ravulizumab is likely to be safe for humans?

Research has shown that ravulizumab is generally safe for people with IgA nephropathy. In past studies, participants taking ravulizumab experienced side effects similar to those taking a placebo, a harmless pill with no active ingredients. This indicates that the treatment did not cause more side effects than the placebo, suggesting its safety. Ravulizumab has been used for years to treat other conditions, maintaining a strong safety record. While some side effects can occur, they are usually mild and comparable to those of other treatments.12345

Why do researchers think this study treatment might be promising?

Ravulizumab is unique because it offers a new approach for treating IgA nephropathy by targeting and inhibiting the complement system, which plays a key role in the disease. Unlike standard treatments that often involve immunosuppressive drugs, Ravulizumab specifically blocks the C5 protein in the complement pathway, potentially reducing inflammation and kidney damage more effectively. Researchers are excited about this treatment because it only requires infusions every 4 to 8 weeks, which could be more convenient for patients compared to the more frequent dosing schedules of existing therapies.

What evidence suggests that ravulizumab might be an effective treatment for IgA nephropathy?

Research has shown that ravulizumab, the investigational treatment in this trial, may effectively treat IgA nephropathy, a kidney condition. One study found it reduced protein in the urine by 41.9% compared to a placebo over 26 weeks. Lowering protein in the urine helps protect the kidneys. Another study reported a 30.1% reduction in protein levels after about six months. Patients taking ravulizumab also maintained stable kidney function, as measured by the eGFR test, and the treatment was generally well-tolerated. These findings suggest that ravulizumab could be a helpful option for managing IgA nephropathy.12356

Are You a Good Fit for This Trial?

This trial is for children with a kidney disease called IgA Nephropathy, which can cause blood in urine and joint pain. It's also open to those with related conditions like Henoch-Schönlein Purpura that leads to rash and abdominal pain.

Inclusion Criteria

UPCR ≥ 0.5 g/g from the mean of 3 first morning voids (FMV) collected within 1 week during the Screening Period
I have been vaccinated against meningococcal infection.
My kidney function is within the required range.
See 3 more

Exclusion Criteria

Congenital immunodeficiency
I have been diagnosed with hemolytic uremic syndrome.
My IgA nephropathy is not a primary condition or related to IgAV.
See 10 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive a weight-based loading dose of ravulizumab on Day 1, followed by weight-based maintenance treatment on Day 15 and either once every 8 weeks or once every 4 weeks depending on weight

Variable, based on weight
Initial visit on Day 1, follow-up visits on Day 15 and every 4 or 8 weeks

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Ravulizumab
Trial Overview The study tests Ravulizumab, given through an IV, focusing on how the body processes it (PK) and its effects (PD). The goal is to see if what works for adults can be applied to kids.
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: RavulizumabExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Alexion Pharmaceuticals, Inc.

Lead Sponsor

Trials
267
Recruited
141,000+
Dr. Alberto R. Martinez profile image

Dr. Alberto R. Martinez

Alexion Pharmaceuticals, Inc.

Chief Medical Officer since 2010

MD from University of Sao Paulo

Marc Dunoyer profile image

Marc Dunoyer

Alexion Pharmaceuticals, Inc.

Chief Executive Officer since 2021

PhD in Molecular Biology

Citations

1.pubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov/39455063/
Efficacy and Safety of Ravulizumab in IgA NephropathyAt week 26, a statistically significant reduction in proteinuria was observed with ravulizumab versus placebo: −41.9% (95% confidence interval [ ...
Efficacy and Safety of Ravulizumab in IgA NephropathyA 30.1% (90% confidence interval, 13.7% to 43.5%) relative reduction in proteinuria for ravulizumab versus placebo was observed at approximately 6 months.
NCT06291376 | Study of Ravulizumab in Immunoglobulin ...The primary objective of this study to evaluate efficacy of ravulizumab compared with placebo on proteinuria reduction and change in eGFR in adult participants ...
WCN24-1197 EFFICACY AND SAFETY OF ...In ravulizumab-treated pts, proteinuria reduction was rapid and sustained through week 26 (Figure 1) and eGFR remained stable. Ravulizumab was well-tolerated ...
WCN24-1197 EFFICACY AND SAFETY OF ...In ravulizumab-treated pts, proteinuria reduction was rapid and sustained through week 26 (Figure 1) and eGFR remained stable. Ravulizumab was well-tolerated ...
145 Subgroup and secondary endpoint evaluation of a phase ...The SANCTUARY RCT evaluated ravulizumab (IV; weight-based dosing Q8W) vs placebo in adults with primary IgA nephropathy. Randomized patients (2: ...
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