← Back to Search

Janus Kinase Inhibitor

Baricitinib for Chronic Kidney Disease (JUSTICE Trial)

Phase 2
Recruiting
Led By Opeyemi Olabisi, MD
Research Sponsored by Duke University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Adults 18-70 years
FSGS diagnosed by kidney biopsy or clinically diagnosed HTN-CKD
Must not have
Current use of potent immunosuppressants such as abatacept, adalimumab, anakinra, azathioprine, certolizumab, etanercept, golimumab, infliximab, probenecid, rituximab, ruxolitinib, sarilumab, tofacitinib, or tocilizumab
Previous kidney transplant
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years

Summary

This trial is testing if baricitinib can safely reduce high levels of albumin in the urine for African American/Blacks with certain kidney conditions. The drug works by reducing inflammation in the kidneys. Baricitinib has been previously tested for its effectiveness in reducing albumin in adults with Type 2 diabetes who are at high risk for worsening kidney disease.

Who is the study for?
This trial is for African American/Black adults aged 18-70 with high-risk APOL1 genotype, diagnosed FSGS or HTN-CKD without diabetes, HIV, sickle cell disease, recent serious infections, previous kidney transplant, certain liver conditions or low blood counts. Participants must have stable blood pressure and not be on potent immunosuppressants.
What is being tested?
The study tests if baricitinib can safely reduce albuminuria in patients with APOL1-associated kidney diseases compared to a placebo. It's focused on those who don't have diabetes but suffer from FSGS or chronic kidney disease due to hypertension.
What are the potential side effects?
Baricitinib may cause side effects like infection risk increase due to immune system suppression, potential liver enzyme elevation which could indicate liver injury, and possibly changes in blood cell counts leading to anemia or increased bleeding/infection risk.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I am between 18 and 70 years old.
Select...
I have been diagnosed with FSGS or have high blood pressure-related kidney disease.
Select...
I have a high-risk APOL1 genotype.
Select...
My kidney function test shows a rate of at least 26 ml/min.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
Select...
I am currently taking strong medications to suppress my immune system.
Select...
I have had a kidney transplant.
Select...
I have been treated with a JAK inhibitor before.
Select...
My liver tests are higher than normal due to chronic liver disease.
Select...
I am HIV positive.
Select...
I have sickle cell disease.
Select...
I am currently fighting a serious infection.
Select...
My kidney disease is identified as the tip variant of FSGS.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 years for reporting.

Treatment Details

Side effects data

From 2015 Phase 3 trial • 1307 Patients • NCT01710358
5%
Nasopharyngitis
3%
Pharyngitis
2%
Urinary tract infection
2%
Bronchitis
1%
Back pain
1%
Upper respiratory tract infection
100%
80%
60%
40%
20%
0%
Study treatment Arm
Adalimumab Treatment B
BaricitinibTreatment B
Baricitinib Follow-up
Placebo Follow-up
Placebo Treatment B
Adalimumab Follow-up
Baricitinib Treatment A
Adalimumab Treatment A
Placebo Treatment A
Rescue

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: BaricitinibExperimental Treatment1 Intervention
Participants will take one pill of Baricitinib daily with their regular medications.
Group II: PlaceboPlacebo Group1 Intervention
Participants will take a Baricitinib placebo pill matching Baricitinib daily with their regular medications.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Baricitinib
2017
Completed Phase 3
~9510

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 Chronic Kidney Disease (CKD) include angiotensin-converting enzyme (ACE) inhibitors, angiotensin II receptor blockers (ARBs), and Janus Kinase (JAK) inhibitors like Baricitinib. ACE inhibitors and ARBs work by reducing blood pressure and proteinuria, thereby slowing the progression of kidney damage. JAK inhibitors, such as Baricitinib, target the JAK-STAT signaling pathway, which is involved in inflammation and immune responses. By inhibiting this pathway, JAK inhibitors can reduce inflammation and potentially decrease the progression of kidney disease. These mechanisms are crucial for CKD patients as they help manage symptoms, reduce complications, and slow disease progression, improving overall quality of life.
Evidence-Based Medical Therapy in Patients With Heart Failure With Reduced Ejection Fraction and Chronic Kidney Disease.Effects of oral alkali drug therapy on clinical outcomes in pre-dialysis chronic kidney disease patients: a systematic review and meta-analysis.Socio-economic impact in CKD.

Find a Location

Who is running the clinical trial?

National Institute on Minority Health and Health Disparities (NIMHD)NIH
430 Previous Clinical Trials
1,371,676 Total Patients Enrolled
Duke UniversityLead Sponsor
2,452 Previous Clinical Trials
2,971,716 Total Patients Enrolled
Eli Lilly and CompanyIndustry Sponsor
2,670 Previous Clinical Trials
3,228,694 Total Patients Enrolled

Media Library

Baricitinib (Janus Kinase Inhibitor) Clinical Trial Eligibility Overview. Trial Name: NCT05237388 — Phase 2
Chronic Kidney Disease Research Study Groups: Placebo, Baricitinib
Chronic Kidney Disease Clinical Trial 2023: Baricitinib Highlights & Side Effects. Trial Name: NCT05237388 — Phase 2
Baricitinib (Janus Kinase Inhibitor) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05237388 — Phase 2
~34 spots leftby Mar 2026