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Henlius Forecasts Profit in 2023 H1: Spurring a Seamless R&D, Manufacturing, and Commercialisation Positive Cycle

2023-07-03

Shanghai, China, July 3rd, 2023 – Henlius (2696.HK) released a positive profit forecast. Based on the preliminary assessment of the unaudited comprehensive management accounts for the six months ended June 30, 2023, the company expects to turn into profits in the first half of 2023, achieving profitability for the first time in a six-month period. The company expects a profit of approximately RMB200 million during the reporting period, primarily contributed by the continuous growth in sales revenue of the company's core products HANQUYOU and HANSIZHUANG, as well as a careful cost control through slimmed down business operations.


Wenjie Zhang, Chairman, Executive Director and Chief Executive Officer of Henlius, remarked: “In the first half of 2023, we have entered a very positive cycle and achieved high-quality development at both the corporate and business levels as a result of our constant desire for self-improvement. Looking ahead, we will continue to prioritize clinical needs, drive cost reduction and efficiency by lean operation, uphold self-development and innovation, and strengthen the synergy between R&D, manufacturing, and commercialisation, and consistently introduce competitive products to contribute to the well-being of patients.”


Accelerating Revenue, Leading Sustainable Growth


In the first half of 2023, Henlius further enhanced its self-sufficiency capabilities and actively advanced new business models. The company continuously optimized its commercialisation layout and achieved remarkable results. With a focus on core oncology and immunotherapy products, Henlius established a professional and efficient commercialisation team, driving the commercialisation process of each product, enhancing accessibility of drugs from multiple dimensions, and providing high-quality services to clinicians with solid expertise and prompt and effective response, thus maximizing the benefits for patients. The revenue growth was led by the outstanding performance of the company's two core products, which also achieved significant milestones in the mainstream biologics markets in Europe and the United States, further cementing Henlius’ reputation as a domestic biopharma leader.

 

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HANQUYOU (trastuzumab, trade name in Europe: Zercepac®; trade names in Australia: Tuzucip® and Trastucip®), indicated for the treatment of HER2-positive breast cancer and gastric cancer, is the first product sold and promoted in Chinese mainland by the company’s in-house commercialisation team. In the first quarter of 2023, the domestic sales revenue reached approximately RMB538.6 million, representing a year-on-year increase of approximately 66.7%. In China, HANQUYOU has been widely used in clinical practice due to its advantages such as dual dosage, "ready-to-use" formulation, and preservative-free formulation. To date, both the 150mg and 60mg form of HANQUYOU were included in the medical insurance procurement platform for all provinces in the Chinese mainland, benefiting over 140,000 Chinese patients. In terms of overseas markets, as a pioneer biologic in the "going global", HANQUYOU was approved for commercialisation by the European Commission (EC) in July 2020 and has by far successfully secured marketing approvals in over 30 countries and regions, including the United Kingdom, Switzerland, Australia, Singapore, Argentina, and Saudi Arabia. Notably, the Biologics License Application (BLA) for HANQUYOU has been accepted by the U.S. Food and Drug Administration (FDA) in the first half of 2023, which will further expand the product’s footprint and benefit patients in major markets of biologics in the U.S. and Europe.

 

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The company's first innovative product, HANSIZHUANG (serplulimab), was approved in China in March 2022. By the end of 2022, after 9 months on the market, it achieved sales revenue of RMB339.1 million, and in the first quarter of 2023, the domestic sales revenue reached approximately RMB249.8 million. In March 2023, the product realized a monthly sale of over RMB100 million in Chinese mainland, starting a new stage of its sales growth as well as providing strong momentum for the product’s commercialisation. At present, HANSIZHUANG has been approved for 3 indications in China including MSI-H solid tumour, squamous non-small cell lung cancer (sqNSCLC) and extensive stage small cell lung cancer (ES-SCLC). It is also the world's first anti-PD-1 monoclonal antibody (mAb) for the first-line treatment of SCLC. With its breakthrough efficacy and differentiation advantages in the relevant treatment fields, HANSIZHUANG has earned wide recognitions and has seen rapid sales uptick. Pivotal clinical research results have been published in leading medical journals such as the Journal of the American Medical Association (JAMA, Impact Factor: 157.3), contributing to rapid market expansion. As of June 2023, HANSIZHUANG has completed the tendering process in multiple provinces in China, covering nearly a thousand hospitals in relevant departments. The company has also continued to enrich multi-level medical coverage, successfully promoting the inclusion of HANSIZHUANG in customized supplementary medical insurance directories in cities such as Shanghai, Ningbo, Xiamen, Wuxi, and Kunming. In March 2023, the European Medicines Agency (EMA) has validated the Marketing Authorization Application (MAA) for HANSIZHUANG for the first-line treatment of ES-SCLC, and plans are underway to submit a Biologics License Application (BLA) for it in the U.S. in 2024, presenting broader opportunities and growth prospects for the company.


Cementing Foundations for a More Resilient Future


As a global biopharmaceutical company, Henlius is committed to providing affordable and high-quality biologics to patients worldwide with a focus on oncology, autoimmune diseases, and ophthalmic diseases. Up to date, 5 products have been launched in China, 1 has been approved for marketing in overseas markets, 18 indications are approved worldwide, and 3 marketing applications have been accepted for review in China, the U.S., and the EU, respectively. Incorporating high-efficiency and innovation into its integrated biopharmaceutical platform, the company actively enhances its competitiveness and solidifies the foundation for long-term business development through the entire product life cycle, including R&D, manufacturing and commercialisation. The three production facilities, Xuhui Facility, Songjiang First Plant and Songjiang Second Plant, can altogether reach a larger operational scale with the total commercial production capacity expected to reach 144,000 litres in 2026, further offering a strong support for the company’s global market expansion in the medium to long term.

 

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In terms of R&D, Henlius emphasizes clinical needs and cutting-edge technologies. The company continuously adjust and optimize its research layout and have established innovation centres in Shanghai and California. These two locations synergistically enhance the efficiency and quality of its R&D. Additionally, Henlius actively collaborates with leading academic institutions and global partners worldwide to explore technological innovations and frontier applications. By integrating internal and external resources and professional teams, Henlius is accelerating the development of innovative and differentiated therapies, providing patients with more effective and precise treatment options. Currently, Henlius has pro-actively built a diversified and high-quality product pipeline, including over 50 molecules, and are advancing immuno-oncology combination therapies with proprietary HANSIZHUANG as backbone. Meanwhile, Henlius has conducted over 30 clinical studies for 16 products globally, with independent development accounts for over 80% of the product pipeline.

 

Moving forward, Henlius will continue to prioritize high-quality development and lean operations, deepen product innovation, expand market presence, and foster global collaborations to offer high-quality, affordable, and innovative medicines to patients worldwide.

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