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Design and Rationale of the Phase 2 Baricitinib Study in Apolipoprotein L1-Mediated Kidney Disease (JUSTICE).

Publication ,  Journal Article
Olabisi, OA; Barrett, NJ; Lucas, A; Smith, M; Bethea, K; Soldano, K; Croall, S; Sadeghpour, A; Chakraborty, H; Wolf, M
Published in: Kidney Int Rep
September 2024

INTRODUCTION: Individuals of recent West African ancestry develop focal segmental glomerulosclerosis (FSGS) and hypertension-attributed end-stage kidney disease (HTN-ESKD) at 4 times the rate of White Americans. Two protein-coding variants of the Apolipoprotein L1 (APOL1) gene, G1 and G2, explain 50% to 70% of the excess risk of HTN-ESKD and FSGS among this group. Increased expression of G1 and G2 in the kidney, mediated by Janus kinase/signal transducer and activator of transcription (JAK-STAT) signaling, drive pathogenesis of these kidney diseases. Baricitinib is an orally active inhibitor of JAK1/2 that blocks APOL1 synthesis. The Janus kinase-STAT Inhibition to Reduce APOL1-Associated Kidney Disease (JUSTICE) trial is evaluating the antiproteinuric efficacy and safety of baricitinib in patients with APOL1-associated FSGS and HTN-attributed chronic kidney disease (HTN-CKD). METHODS: JUSTICE is a single-center, randomized, double-blind, placebo-controlled, pilot phase 2 trial of baricitinib in patients with proteinuria, APOL1-associated FSGS or APOL1-associated HTN-CKD without diabetes. A total of 75 African American patients with APOL1-associated CKD, including 25 with FSGS and 50 with HTN-CKD, aged 18 to 70 years will be randomized 2:1 to daily treatment with baricitinib or placebo, respectively. RESULTS: The primary efficacy end point will be percent change in urine albumin-to-creatinine ratio (UACR) from baseline to end of month 6. The primary safety end point will be incidence of clinically significant decreases in hemoglobin of ≥ 1g/dl. CONCLUSION: The phase 2 JUSTICE study will characterize the antiproteinuric efficacy and safety of JAK1/2 inhibition with baricitinib in patients with APOL1-associated FSGS and APOL1-associated HTN-CKD.

Duke Scholars

Published In

Kidney Int Rep

DOI

EISSN

2468-0249

Publication Date

September 2024

Volume

9

Issue

9

Start / End Page

2677 / 2684

Location

United States

Related Subject Headings

  • 42 Health sciences
  • 32 Biomedical and clinical sciences
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Olabisi, O. A., Barrett, N. J., Lucas, A., Smith, M., Bethea, K., Soldano, K., … Wolf, M. (2024). Design and Rationale of the Phase 2 Baricitinib Study in Apolipoprotein L1-Mediated Kidney Disease (JUSTICE). Kidney Int Rep, 9(9), 2677–2684. https://doi.org/10.1016/j.ekir.2024.06.033
Olabisi, Opeyemi A., Nadine J. Barrett, Anika Lucas, Maurice Smith, Kenisha Bethea, Karen Soldano, Stephanie Croall, Azita Sadeghpour, Hrishikesh Chakraborty, and Myles Wolf. “Design and Rationale of the Phase 2 Baricitinib Study in Apolipoprotein L1-Mediated Kidney Disease (JUSTICE).Kidney Int Rep 9, no. 9 (September 2024): 2677–84. https://doi.org/10.1016/j.ekir.2024.06.033.
Olabisi OA, Barrett NJ, Lucas A, Smith M, Bethea K, Soldano K, et al. Design and Rationale of the Phase 2 Baricitinib Study in Apolipoprotein L1-Mediated Kidney Disease (JUSTICE). Kidney Int Rep. 2024 Sep;9(9):2677–84.
Olabisi, Opeyemi A., et al. “Design and Rationale of the Phase 2 Baricitinib Study in Apolipoprotein L1-Mediated Kidney Disease (JUSTICE).Kidney Int Rep, vol. 9, no. 9, Sept. 2024, pp. 2677–84. Pubmed, doi:10.1016/j.ekir.2024.06.033.
Olabisi OA, Barrett NJ, Lucas A, Smith M, Bethea K, Soldano K, Croall S, Sadeghpour A, Chakraborty H, Wolf M. Design and Rationale of the Phase 2 Baricitinib Study in Apolipoprotein L1-Mediated Kidney Disease (JUSTICE). Kidney Int Rep. 2024 Sep;9(9):2677–2684.
Journal cover image

Published In

Kidney Int Rep

DOI

EISSN

2468-0249

Publication Date

September 2024

Volume

9

Issue

9

Start / End Page

2677 / 2684

Location

United States

Related Subject Headings

  • 42 Health sciences
  • 32 Biomedical and clinical sciences