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Wuhan Hiteck Biological Pharma Co Ltd

Wuhan Hiteck Biological Pharma Co., Ltd. is a biopharmaceutical company founded in 1992 and based in Wuhan, China. It produces and sells bioengineering products and lyophilized powder injections in China and internationally. The company operates through segments including Biopharmaceutical; Pharmaceutical Technology Services; In Vitro Diagnostic Reagents; Production and Sales of Active Pharmaceutical Ingredients and Pharmaceutical Intermediates; and Other. Its products include injectables such as Epramine, mouse nerve growth factor, omeprazole sodium, esomeprazole sodium, and cyclic adenosine monophosphate; oral formulations such as tinidazole suppository, acyclovir dispersible tablets, nimodipine extended-release tablets, trimetazidine hydrochloride tablets, and azithromycin granules; and diagnostic kits for measles, rubella, mycoplasma, bacterial vaginosis, novel coronavirus N-Protein, and various IgG and IgM antibodies, as well as a thalassemia diagnostic kit. It also offers Lopinavir and Ritonavir APIs and intermediates, serving the nervous system and oncology fields.

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Hite Biological's 2026 interim report shows net loss widening to 78.71 million yuan

Hite Biological released its 2026 interim report, with net profit attributable to the parent company at minus 78.71 million yuan, a loss expansion of 39.53 million yuan compared with the same period last year. The company's total operating revenue was 226 million yuan, down 18.01 percent year on year. Net cash outflow from operating activities was 2.87 million yuan, the asset-liability ratio rose to 15.43 percent, gross margin fell to 34.25 percent, and diluted earnings per share was minus 0.60 yuan.
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Biotech & Genomic Medicine

Haitai Biological's Investee Company Zhongmou Medical Receives Clinical Trial Approval for ZM-02 Ophthalmic Injection

Haitai Biological's investee company Zhongmou Medical has received clinical trial approval from the National Medical Products Administration for its independently developed ZM-02 ophthalmic injection, intended for the treatment of advanced retinitis pigmentosa. The drug is a Class 1 therapeutic biological product and represents a new-generation optogenetic gene therapy. It delivers a novel light-sensitive protein gene through a single intravitreal injection and can be broadly applied to both inherited and acquired retinal degenerative diseases. The drug previously obtained orphan drug designation from the U.S. FDA in October 2024. The company cautions that drug development involves high investment and high risk and will not affect near-term financial performance.
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Biotech & Genomic Medicine

Haitai Bio's Injectable Epunaiming Clinical Trial Application for New Indication Accepted

Haitai Bio announced that the clinical trial application for its injectable Epunaiming for the indication of unresectable or metastatic classic chondrosarcoma has been accepted by the National Medical Products Administration. The drug is a national Class I recombinant protein innovative drug independently developed by the company, and is the world's first and only marketed death receptor 4/death receptor 5 agonist. Currently, no drug has been approved for the chondrosarcoma indication. The drug has a long development cycle and high risks, and will not have a material impact on the company's performance in the short term.
Biotech & Genomic Medicine2

Clinical Trial Application for Injectable Epratuzumab for Classic Chondrosarcoma Accepted

Wuhan Hiteck Biological Pharma's clinical trial application for injectable epratuzumab, brand name Shaite, for the indication of unresectable or metastatic classic chondrosarcoma has been accepted by the National Medical Products Administration. The drug is a national Class I recombinant protein innovative drug independently developed by the company, and is the world's first and only marketed death receptor 4/death receptor 5 agonist. Chondrosarcoma is the second most common primary malignant bone tumor, with an incidence of about one in two hundred thousand. It is typically resistant to radiotherapy and conventional chemotherapy, and to date no drug has been approved for this indication. An investigator-initiated trial of epratuzumab monotherapy for advanced chondrosarcoma showed some tumor-suppressive effect, and non-clinical and clinical studies indicate that drugs targeting DR4/DR5 have good efficacy against chondrosarcoma.
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Haitai Biological posts widening losses for four straight years, faces barrage of investor questions at earnings briefing

Haitai Biological faced intense questioning from investors at its earnings briefing, as the company has now recorded four consecutive years of losses with the deficit widening. In 2025, revenue reached 541 million yuan, down 16.57 percent year-on-year, while the net loss attributable to shareholders was 231 million yuan, compared with a loss of 69.35 million yuan a year earlier. In the first quarter of 2026, revenue came in at 159 million yuan, up 1.52 percent year-on-year, with a net loss attributable to shareholders of 23.05 million yuan, versus a loss of 13.93 million yuan in the same period last year. Investors repeatedly pressed on whether the company can return to profit this year and how much profit its main product, Eprinomectin, can generate. The company responded that its core business operations are steadily improving and it will make every effort to drive operational improvements and strive to turn profitable as soon as possible. Eprinomectin production capacity became the focal point of the meeting, with multiple investors asking in succession why the previously mentioned capacity release in 2026 had disappeared. The company clarified that the newly designed capacity is 1.2 million units, with the additional capacity expected to come on stream in the second half of next year, and that there is no scenario of capacity being released ahead of schedule in 2026. It stressed that the product has been included in the national medical insurance scheme and that in 2026 it will basically achieve full production and full sales. The subsidiary Jingmen Hanrui continues to be a drag on the listed company. Investors questioned whether the CDMO layout was a mistake and why the CRO referral ratio is too low. The company said Hanrui is mainly engaged in the production and sale of active pharmaceutical ingredients and intermediates, and it will push for continued loss reduction at the unit. In addition, investors expressed concern over the single-product pipeline. The company disclosed that in oncology it is advancing research on a new indication for Eprinomectin in chondrosarcoma, while in the neurology field its recombinant human nerve growth factor eye drop project is in clinical phase Ib, and it is simultaneously building multiple technology platforms. In the secondary market, as of the close on July 10, Haitai Biological shares rose 5.28 percent to 25.92 yuan per share, giving it a total market capitalisation of about 3.393 billion yuan. The stock has fallen about 6.53 percent so far this year.
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