HENGRUI PHARMA's ω-3 Triglyceride (2%) MCT/LCT Fat Emulsion/Amino Acids (16)/Glucose (30%) Receives Drug Registration Approval

Stock News
05/19

HENGRUI PHARMA announced that its subsidiary, Fujian Shengdi Pharmaceutical Co., Ltd., has received notification from the National Medical Products Administration that the ω-3 Triglyceride (2%) Medium/Long-Chain Fat Emulsion/Amino Acids (16)/Glucose (30%) Injection has been approved for marketing. Severe catabolism is commonly observed in clinical scenarios such as the perioperative period, malignancies, severe infections, major trauma, and sepsis. Patients in these conditions often experience high metabolic stress and impaired nutrient intake, which can easily lead to malnutrition, decreased immunity, delayed wound healing, increased risk of complications, significantly prolonged hospital stays, and adverse impacts on long-term survival prognosis. This represents a critical issue in clinical comprehensive treatment that urgently needs resolution.

The ω-3 Triglyceride (2%) Medium/Long-Chain Fat Emulsion/Amino Acids (16)/Glucose (30%) Injection is packaged in a three-chamber bag, with ω-3 Triglyceride (2%) Medium/Long-Chain Fat Emulsion Injection, Compound Amino Acids (16) Injection, and Compound Glucose (30%) Injection stored in three separate chambers. Before use, pressing or squeezing the package bag causes the solutions to break the isolation strips, enabling rapid mixing of the three solutions to form a composite injection, offering convenient operation. Studies indicate that the three-chamber bag is more cost-effective and provides better sterility assurance compared to hospital-prepared "all-in-one" parenteral nutrition solutions, leading to its increasing recognition in clinical use.

The original ω-3 Triglyceride (2%) Medium/Long-Chain Fat Emulsion/Amino Acids (16)/Glucose (30%) Injection was developed by B.Braun Melsungen AG and was approved for marketing in multiple European countries, including Germany, France, the UK, and Italy, in 2010. The company's current approval is considered as passing the generic drug quality and efficacy consistency evaluation. To date, the cumulative research and development investment for the ω-3 Triglyceride (2%) Medium/Long-Chain Fat Emulsion/Amino Acids (16)/Glucose (30%) Injection-related project amounts to approximately RMB 83.9 million (unaudited).

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