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Hyaluronic acid

Generic Name
Hyaluronic acid
Drug Type
Small Molecule
Chemical Formula
C28H44N2O23
CAS Number
9004-61-9
Unique Ingredient Identifier
S270N0TRQY

Overview

Hyaluronic acid (HA) is an anionic, nonsulfated glycosaminoglycan found in connective, epithelial, and neural tissues; it was first isolated in 1934. Karl Meyer and John Palmer obtained glycosaminoglycan (GAG) from the bovine eye, giving it the name “hyaluronic acid”. HA is involved in many important physiological processes, including but not limited to wound healing, tissue regeneration, and joint lubrication. It demonstrates unique viscoelasticity, moisturizing, anti-inflammatory qualities, and other important properties that prove beneficial in various clinical applications. HA is used in drug delivery systems for the treatment of cancer, ophthalmological conditions, joint conditions, and aesthetic imperfections. Several preparations of hyaluronic acid have been approved by the FDA and are available in oral, topical, and injectable forms. A popular use of hyaluronic acid in recent years is cosmetic injection due to its ability to minimize the appearance of wrinkles and aging-related skin imperfections.

Indication

The intra-articular preparations of hyaluronic acid are indicated for knee pain associated with osteoarthritis. Hyaluronic acid is used in cosmetic applications to prevent and reduce the appearance of wrinkles on the face, and as a dermal filler to correct facial imperfections or other imperfections on other parts of the body. It is frequently an ingredient in topical applications for wound healing and symptomatic treatment of skin irritation from various causes. Hyaluronic acid may also be indicated in ophthalmological preparations or oral capsules to treat discomfort caused by dry eyes or conjunctivitis and for its protective qualities during and before eye surgery. Finally, hyaluronic acid can be used off-label to coat the bladder for relief of interstitial cystitis symptoms.

Associated Conditions

  • Actinic Keratosis (AK)
  • Burns
  • Chronic Skin Ulcers
  • Conjunctivitis
  • Dehydration
  • Dermabrasion
  • Dermatosis
  • Dry Eyes
  • Facial Defect
  • Interstitial Cystitis
  • Keratoconjunctivitis
  • Ocular Irritation
  • Osteoarthritis (OA)
  • Pain of the knee
  • Seasonal Allergic Conjunctivitis
  • Skin Burn
  • Skin Irritation
  • Skin fissures
  • Tissue Adhesions
  • Varicose Ulcers
  • Wound
  • Eye discomfort
  • Facial fine wrinkling
  • Sensation of burning in the eyes
  • Superficial Wounds

Research Report

Published: Aug 1, 2025

A Comprehensive Monograph on Hyaluronic Acid (DB08818): From Foundational Biomaterial to Advanced Therapeutic Platform

Executive Summary

Hyaluronic Acid (HA), identified by DrugBank ID DB08818, is a ubiquitous and multifunctional glycosaminoglycan that is integral to the structure and function of vertebrate tissues. Chemically, it is a simple, linear polysaccharide, yet its biological role is remarkably complex and fundamentally dictated by its molecular weight. This report provides an exhaustive analysis of HA, covering its history, chemical properties, multifaceted pharmacology, extensive clinical applications, safety profile, and global regulatory status.

The core of HA's function lies in its dual nature. As a high-molecular-weight (HMW) polymer, it serves as a passive structural molecule, leveraging its unique viscoelastic and hygroscopic properties to lubricate joints, hydrate tissues, and provide shock absorption. In this capacity, it is a cornerstone of therapies for osteoarthritis and a primary component of ophthalmic surgical aids. Conversely, as a low-molecular-weight (LMW) fragment, HA acts as an active signaling molecule. By interacting with cell surface receptors such as CD44, it can initiate pro-inflammatory and angiogenic cascades essential for tissue repair and wound healing. This size-dependent dichotomy is a central theme in its pharmacology and explains its diverse, and at times seemingly contradictory, biological effects.

Clinically, HA's utility is most established in three key areas: orthopedics, for the viscosupplementation of osteoarthritic joints; aesthetic medicine, as the gold-standard biodegradable dermal filler for soft tissue augmentation; and ophthalmology, as an indispensable viscoelastic tool in ocular surgery. Its safety profile is excellent, with most adverse events being mild, transient, and related to the injection procedure rather than the material itself.

Continue reading the full research report

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2025/06/10
Phase 1
Not yet recruiting
2025/04/20
Phase 4
Not yet recruiting
2025/02/10
Not Applicable
Not yet recruiting
Beijing Tongren Hospital
2024/11/29
Not Applicable
Completed
2024/11/19
Phase 1
Recruiting
Basel khaled mohamed
2024/11/12
Phase 3
Completed
Federico II University
2024/10/24
Not Applicable
Not yet recruiting
He Eye Hospital
2024/09/26
Phase 2
Not yet recruiting
Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
2024/08/26
Phase 3
Recruiting
Wuxi Cellular Biopharmaceutical Group Ltd.
2024/08/09
Phase 1
Recruiting
Beijing Tongren Hospital

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Sincerus Florida, LLC
72934-2090
TOPICAL
0.5 g in 100 g
4/23/2019
IDO PHARM
77039-034
TOPICAL
0.0000001 g in 1 mL
6/10/2025
Sincerus Florida, LLC
72934-2098
TOPICAL
2 g in 100 g
5/21/2019
Quimfa S.A
77651-4162
INTRAEPIDERMAL
2.5 g in 1 1
6/5/2020
SUPERBLIC Inc.
86243-0002
TOPICAL
0.18 g in 100 mL
9/2/2025
Sincerus Florida, LLC
72934-2091
TOPICAL
0.5 g in 100 g
4/23/2019
Shantou Youjia E-Commerce Co., Ltd.
84067-150
CUTANEOUS
17 mg in 100 mg
3/11/2024
Sinceru Florida, LLC
72934-2096
TOPICAL
1 g in 100 g
4/24/2019
Sincerus Florida, LLC
72934-2092
TOPICAL
0.5 g in 100 g
4/23/2019

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
HYALGAN INJECTION 20 mg/2 ml
SIN06242P
INJECTION
20 mg/2 ml
6/22/1991
NEPHROSTERIL FOR INTRAVENOUS INFUSION
SIN06299P
INJECTION
1.5 g/l
6/21/1991

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
No Health Canada approvals found for this drug.

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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