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Study identifier: NCT02952144 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Post Approval Study of Lixelle for the Treament of Dialysis-Related Amyloidosis

Condition: Dialysis Amyloidosis  ·  Sponsor: Kaneka Medical America LLC

PhaseNA
Planned participants40
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

Dialysis-related amyloidosis (DRA) is a serious complication of long-term hemodialysis (HD). Its pathogenic mechanism involves accumulation of β2-microglobulin (β2M) in the blood. β2M is produced by most cells in the body and is metabolized in the kidney in healthy individuals. However, in HD patients with renal dysfunction, β2M which is not removed entirely by HD accumulates excessively in the blood. Then it forms amyloid fibrils that are deposited in bones, joints, and soft tissues. The fibrils are further modified by advanced glycation end products (AGE), inducing local macrophage infiltration and production of cytokines leading to chronic inflammation and activation of osteoclasts. Consequently, severe complications with various symptoms are developed, which are collectively referred to as DRA. Lixelle® is a whole-blood β2M apheresis column developed to adsorb and eliminate β2M selectively from the blood of DRA patients. The treatment is performed with Lixelle® connected upstream of the dialyzer in series on a HD circuit in every session. The Lixelle® column contains porous cellulose beads with covalently linked hexadecyl alkyl chain ligands, which selectively adsorb β2M, via a molecular sieving effect because of its porous structure and hydrophobic interaction with ligands. Lixelle® has been used to relieve symptoms and prevent the progression of DRA in Japan since 1996, when health insurance coverage and reimbursement for the treatment were approved by Japanese Ministr…

This description comes directly from the study's public registry record.

Talk to the study team

Joanne McLaughlin  ·  (646) 202-3566  ·  joanne.mclaughlin@kaneka.com

Always discuss trial participation with your own doctor first.

Locations (1)

The Rogosin InstituteNew York, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT02952144