重组人白蛋白注射液(水稻)(奥福民)
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“稻米造血”引资本追捧,禾元生物市值冲高 血制品行业影响几何?
Mei Ri Jing Ji Xin Wen· 2025-10-29 15:00
Core Viewpoint - He Yuan Bio's innovative "rice blood production" technology aims to revolutionize the production of human serum albumin, traditionally reliant on human plasma extraction, thus addressing supply shortages and reducing virus transmission risks [1][2]. Company Overview - He Yuan Bio, founded by Professor Yang Daichang's team from Wuhan University, recently launched its core product, HY1001 (recombinant human albumin injection), becoming the first plant-derived recombinant human albumin drug approved in China [1][2]. - The company made a significant market impact, with its stock price surging over 200% on its debut on the STAR Market, leading to a market capitalization exceeding 40.5 billion yuan [2]. Technology and Innovation - The "rice blood production" technology involves inserting the human serum albumin gene into rice cells, allowing for the extraction and purification of recombinant human serum albumin with a purity of 99.9999% [2][4]. - This method not only mitigates the risks associated with plasma extraction but also enhances the domestic supply capability of human serum albumin, which is crucial given the increasing demand and reliance on imports [3][4]. Market Demand and Competition - The demand for human serum albumin in China is projected to grow, with imports accounting for 69% of the supply as of 2024, highlighting a significant gap in domestic production [3]. - He Yuan Bio faces competition from four other companies developing recombinant human albumin products, with the fastest progress seen from Tonghua Anruite, which has already received approval for its product in Russia and Kyrgyzstan [5]. Clinical Applications and Future Plans - The primary clinical application for He Yuan Bio's recombinant human albumin is in treating low albumin levels in liver cirrhosis patients, which constitutes about 30% of the overall market [5]. - The company is also focused on expanding its indications and plans to enter the U.S. market, with a timeline to complete Phase III clinical trials by 2025 and submit a market application in 2026 [6].