TERGASE Inj.
Medicine

TERGASE Inj.

Extremely high purity(99%) Hyaluronidase
- Main Ingredients : Recombinant human hyaluronidase 1500 IU/mL
- Classification : Prescription Drug
- Formulation : Albumin-free and preservative-free liquid formulation
- Efficacy & Effect
• To increase the absorption/dispersion of injected drugs or local anesthetics by subcutaneous or intramuscular injection, and subcutaneous fluid administration
• To improve resorption of excess body fluid and blood in tissue
- Specification : 1.0 mL in 3.0 mL vial, 10 vials/

 

 

Tergaze Inj. is a recombinant human hyaluronidase formulation developed based on Alteogen's proprietary recombinant technology, HYBROZYME™ Technology.

 

 

Active Ingredient

Recombinant human hyaluronidase 1500 IU/mL

(In accordance with Ph. Eur. hyaluronidase assay)

Mechanism of Action and Effects

• Facilitates the absorption and dispersion of drugs and local anesthetics during subcutaneous injection, intramuscular injection, and subcutaneous infusion.

• Promotes the resorption of excess fluids and blood accumulated in tissues.

Product Features

• High-Purity Human-Derived Hyaluronidase:

Enhanced safety is expected due to the reduction of impurities and foreign proteins.

• Superior Safety:

Avoids the risks of viral infection and genotoxicity commonly associated with animal-derived formulations.

• Recombinant DNA Technology:

Manufacturing based on recombinant technology ensures uncompromised product consistency and quality stability.

• Safety Evaluation:

Efficacy and safety evaluations have been successfully completed in large-scale global clinical trials, including in South Korea.

Clinical

Applications

• Plastic Surgery: Breakdown of hyaluronic acid preparations (e.g., fillers) and management of associated side effects. When co-administered during injection therapies aimed at double chin improvement, this formulation promotes the diffusion of the drug within the tissues, contributing to a more uniform local drug distribution. It is also expected to alleviate swelling and pain associated with lifting procedures.

• Internal Medicine / Oncology: Enhancement of drug delivery efficiency and tissue diffusion. 

• Emergency Medicine / Ophthalmology: Emergency management of conditions such as edema and hematomas.

HYBROZYMETM

Technology

 

A proprietary subcutaneous (SC) formulation platform technology developed by the South Korean biotech company Alteogen. It plays a pivotal role in converting oncology and protein drugs—previously limited to intravenous (IV) administration—into SC formulations that enable convenient self-administration at home. This innovative technology has been successfully out-licensed to multiple leading global pharmaceutical companies.

 

• MSD: Signed an exclusive agreement for the subcutaneous formulation of Keytruda, the world's top-selling immunotherapy.

• Daiichi Sankyo: Entered into a technology partnership agreement to develop a subcutaneous formulation of Enhertu, a next-generation oncology drug.

• Global Collaborations: Collaborating with more than six global pharmaceutical companies, including Sandoz and AstraZeneca.

 

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