Drug intelligence / Profile preview

Hyalubrix 60

Development stage
Phase 2
Lead developer
Fidia Farmaceutici
Administration
Intraarticular
01

Overview

Hyalubrix 60 (also marketed as Hyalone) is a sterile, non-pyrogenic, viscoelastic medical device consisting of a 1.5% solution of high molecular weight (>1500 kDa) non-modified sodium hyaluronate (60 mg/4 mL) obtained via bacterial fermentation. Developed and manufactured by Fidia Farmaceutici, it is administered as a single intra-articular injection to temporarily replace synovial fluid in patients suffering from degenerative or mechanical arthropathy of the knee and hip (osteoarthritis). Its primary mechanism of action is viscosupplementation, which restores the viscoelastic properties of the synovial fluid, reduces joint pain, and improves mobility. Hyalubrix 60 has been evaluated in clinical trials, including a Phase II randomized controlled trial conducted by St. Catherine Specialty Hospital comparing its efficacy to autologous microfragmented adipose tissue (MFAT) in patients with Kellgren-Lawrence Grade 2-3 knee osteoarthritis.

Brand names
Hyalubrix 60Hyalubrix60Hyalubrix-60HyaloneHyalubrix
Other names
hyaluronic acid sodium salt 1.5% solutionsodium hyaluronate 1.5% solution
02

Targets

CD44 (CD44 antigen)RHAMM (Hyaluronan-mediated motility receptor)HMMR

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