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HYLAN G-F20

Generic Name
HYLAN G-F20

Overview

No overview information available.

Indication

No indication information available.

Associated Conditions

No associated conditions information available.

Research Report

Published: Nov 1, 2025

Hylan G-F 20 (Synvisc® and Synvisc-One®): A Comprehensive Clinical and Pharmacological Review for the Management of Knee Osteoarthritis

Introduction and Product Profile

Overview of Hylan G-F 20 as a Viscosupplementation Agent

Hylan G-F 20 is a high-molecular-weight, elastoviscous fluid classified as a viscosupplementation agent.[1] It is a sterile, nonpyrogenic, cross-linked derivative of hyaluronan, a naturally occurring glycosaminoglycan that is a critical component of healthy synovial fluid.[3] The primary therapeutic application of Hylan G-F 20 is the treatment of pain associated with osteoarthritis (OA) of the knee.[1] Its place in therapy is specifically for patients who have failed to achieve an adequate response to conservative nonpharmacologic interventions, such as exercise and physical therapy, as well as simple oral analgesics like acetaminophen.[1]

The underlying principle of its use, known as viscosupplementation, is to restore the rheological and physiological properties of the synovial fluid within an osteoarthritic joint.[16] In OA, the endogenous hyaluronan within the synovial fluid becomes depolymerized, leading to a decrease in its molecular weight and concentration. This degradation impairs the fluid's elastoviscous properties, compromising its ability to function as a lubricant and shock absorber, thereby contributing to pain and progressive joint damage.[16] By introducing an exogenous, high-viscosity hyaluronan derivative, Hylan G-F 20 aims to mechanically supplement the pathologic synovial fluid, reduce pain, and improve joint function.[1]

Commercial Formulations: Synvisc® and Synvisc-One®

Hylan G-F 20 is commercially available in two distinct formulations, which share the same active material but differ in their administration protocol:

Continue reading the full research report

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2018/10/03
Phase 4
Terminated
UConn Health
2018/03/30
Phase 4
Completed
2017/03/27
Phase 4
UNKNOWN
2016/02/29
Phase 3
Completed
Fundación Pública Andaluza Progreso y Salud
2016/02/04
Phase 2
Completed
Nature Cell Co. Ltd.
2015/03/17
Phase 4
Completed
Genzyme, a Sanofi Company
2014/07/22
Phase 4
Completed
2013/06/11
Phase 4
Completed
2012/04/26
Phase 4
Completed
2009/09/03
Not Applicable
Withdrawn

FDA Drug Approvals

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No FDA approvals found for this drug.

EMA Drug Approvals

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HSA Drug Approvals

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No HSA approvals found for this drug.

NMPA Drug Approvals

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No NMPA approvals found for this drug.

PPB Drug Approvals

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TGA Drug Approvals

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Health Canada Drug Approvals

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No Health Canada approvals found for this drug.

CIMA AEMPS Drug Approvals

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No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

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No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

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No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

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No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

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No UK EMC drug information found for this drug.

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