Sino Biopharmaceutical Announces 2020 First Quarterly Results

Revenue was approximately RMB6.22 Billion;
Profit Attributable to Owners of the Parent was approximately RMB862 Million

Sino Biopharmaceutical Limited (“Sino Biopharmaceutical” or the “Company”, together with its subsidiaries, the “Group”) (HKEX:1177), a leading, innovative research and development (“R&D”) driven pharmaceutical conglomerate in the PRC, has announced its unaudited first quarterly results for the three months ended 31 March 2020 (“the review period”).

Results Highlights
– At the beginning of the COVID-19 pandemic, owing to its strong sense of social responsibility and in line with its mission, the Group took the initiative to donate RMB10 million to the Chinese Academy of Medical Sciences on 26 January to support research on COVID-19. At the same time, the Group has promptly set up an anti-pandemic supplies procurement team to purchase supplies, such as face masks, protective gloves, protective clothing, negative pressure isolation ambulances and diagnosis and treatment related products, from different countries for donating to anti-pandemic frontline medical workers. Up to the end of the period, Sino Biopharm and its subsidiaries donated cash and supplies on 18 different occasions with a total value of nearly RMB22 million to anti-pandemic efforts.

– “The Establishment and Application of Key Technology Systems on Emulsification in New Pharmaceutical Preparation,” a research project reported by Beijing Tide, in cooperation with Peking University, has been honoured with “The 2019 National Science and Technology Progress Award – Second Prize”. The Group is one of the few pharmaceutical enterprises to be feted in this way. The accolade is prestigious national recognition of Beijing Tide’s research and development platform of emulsification for high-end preparations.

– Construction of “The Purun Bio-Medical’s R&D and Production Project” of Jiangsu Purun Bio-Medical Co., Ltd., a wholly-owned subsidiary of NJCTT located at Nanjing Jiangbei New Materials High-Tech Park, has officially commenced after the groundbreaking ceremony. Occupying an area of about 300 mu, NJCTT’s product R&D and production capabilities would be substantially strengthened after the project is completed.

– The Group has obtained approval from the United States Food and Drug Administration (“FDA”) for its application filed for “Fulvestrant Injection”. This is another advance for the Group to sell its products in the international markets after Tenofovir Disoproxil Fumarate tablets obtained marketing authorization in the European Union.

– During the pandemic, the intravenous therapy of Magnesium Isoglycyrrhizinate injection (brand name: Tianqingganmei) was included as a supportive treatment for patients with mild and common symptoms (without severe underlying illnesses) in the “Treatment Practices for the Mild and Common Cases of Novel Coronavirus Pneumonia (Second Edition)” jointly published by the offices of the National Health Commission and National Administration of Traditional Chinese Medicine.

– Five products including “Budesonide Suspension for Inhalation” (brand name: Tianqingsuchang), “Sitagliptin Phosphate Tablet” and “Dabigatran Etexilate Capsules” (two specifications) obtained approval for drug registration. Three of these products are the first generic drug of their kind in China and have potential to become blockbuster products.

Results
For the three months ended 31 March 2020, the Group recorded revenue of approximately RMB6.22 billion, representing an increase of approximately 0.2% over the same period last year. During the period, profit attributable to the owners of the parent was approximately RMB862 million, approximately 0.6% higher than that of the same period last year. Earnings per share were approximately RMB6.85 cents, 0.7% higher than that of the same period last year. The Group has maintained a strong financial position with cash and bank balances reaching approximately RMB16.12 billion at the period end (as at 31 December 2019: approximately RMB11.91 billion).

The Board of Directors declared a quarterly dividend of HK2 cents per share (2019 first quarter: HK2 cents).

Business Highlights
During the period under review, most outpatient and inpatient visits at hospitals dropped dramatically due to the pandemic. On-site academic activities and face-to-face exchanges with professional doctors were also adversely affected. The Group quickly reacted and fully utilized third-party online academic exchange platforms to maintain communication with general medical practitioners and patients, thereby strengthening its support to online academic activities. Particularly in the areas of respiratory, infection and oncology that have been less affected by the pandemic, intensive online academic exchanges and promotion activities have been launched. The Group has also supported volunteer medical consultations taking place through online hospital networks. The chronic disease management platform of the Group for respiratory, oncology, analgesic, and kidney illnesses that has been actively operating was also used to enhance the service and professional assistance provided to doctors and patients.

For the production, in response to the government’s strategies, the Group has resumed its production and operations at the early stage with strict precautions for isolation and social distancing, with the first priority to ensure the supply of much-needed anti-infection and respiratory drugs for the therapy of those patients infected with COVID-19, as well as the oncology drugs with pressing demand. The respiratory medicine Tianqingsule (Tiotropium Bromide powder for inhalation); anti-infectious medicines Tianjie (Tigecycline for Injection), Fengruineng (Moxifloxacin Hydrochloride and Sodium Chloride Injection), Tianli (Linezolid and Glucose Injections), and Tianming (Caspofungin Acetate for Injection); analgesics Flurbiprofen cataplasm and Parecoxib Sodium for Injection; and orthopedic medicine Gaisanchun (Calcitriol) capsules also recorded strong growth.

The sales from oncology drugs recorded the highest growth among all. In addition to the rapid growth of Anlotinib Hydrochloride capsules, sales of two products: Qingkeshu (Abiraterone Acetate Tablets), and Jizhi (Gefitinib Tablets) rapidly expanded after they secured the bid for the extended centralized drug procurements by the government. Other oncology products Yinishu (Dasatinib) tablets, Qianping (Bortezomib for Injection) and Shoufu (Capecitabine) tablets also recorded strong growth, which further enlarged the sales contribution of the oncology drug lines to the Group.

The newly launched products also significantly boosted the sales growth. In addition to Qingkeshu, and Jizhi mentioned above, products that have been approved for launch also recorded satisfactory results, including cardiovascular medicine Anbeining (Apixaban Tablets), contrast agent Qingliming (Iodixanol Injection), the first generic oncology drug Leweixin (Bendamustine Hydrochloride for Injection), Weishou (Azacitidine for Injection, the first generic drug) and the first generic anti-rheumatic drug Taiyan (Tofacitinib Citrate Tablets).

For R&D, several strategic products with strong potential have secured production approvals during the period, and 4 of them have been designated as meeting the Consistency Evaluation requirements at the same time.

During the review period, the sales performance of the Group’s major medicine types are outlined below:

Hepatitis medicines
– The sales of hepatitis medicines amounted to approximately RMB1,329.61 million, representing approximately 21.4% of the Group’s revenue.

Oncology medicines
– The sales of oncology medicines amounted to approximately RMB1,984.40 million, representing approximately 31.9% of the Group’s revenue.

Orthopedic medicines
– The sales of orthopedic medicines amounted to approximately RMB467.75 million, representing approximately 7.5% of the Group’s revenue.

Anti-infectious medicines
– The sales of anti-infectious medicines amounted to approximately RMB416.01 million, representing approximately 6.7% of the Group’s revenue.

Respiratory system medicines
– The sales of respiratory medicines amounted to approximately RMB334.41 million, representing approximately 5.4% of the Group’s revenue.

Others
– Sales of other medicines amounted to approximately RMB1,689.69 million, representing approximately 27.1% of the Group’s revenue.

R&D
The Group has continued to focus its R&D efforts on new hepatitis, oncology and respiratory system and cardio-cerebral medicines. During the first quarter, the Group was granted 14 clinical trial approvals, 6 production approvals, and 6 approvals for Consistency Evaluation, and made 9 clinical trial applications, 3 applications for Consistency Evaluation and 2 production applications. Cumulatively, a total of 437 pharmaceutical products had obtained clinical trial approval, or were under clinical trial or applying for production approval. Out of these, 30 were for hepatitis medicines, 189 for oncology medicines, 24 for respiratory system medicines, 24 for endocrine, 40 for cardio-cerebral medicines and 130 for other medicines.

Over the years, the Group has been placing high importance on R&D and innovation, as well as through collaboration and imitation, to raise both R&D standards and efficiency. Regarding R&D as the lifeblood of the Group’s development, the Group continues to devote into more resources. For the three months ended 31 March 2020, the total R&D expenditure of approximately RMB994 million, which accounted for approximately 16.0% of the Group’s revenue, was charged to the statement of profit or loss and capitalized in the statement of financial position respectively.

The Group also emphasizes on the protection of intellectual property rights. It encourages its enterprises to apply for patent applications as a means to enhance the Group’s core competitiveness. During the first quarter, the Group has received 25 authorized patent notices (21 invention patents, 2 utility model patents and 2 apparel design patents) and filed 123 new patent applications (120 invention patents and 3 apparel design patents). Cumulatively, the Group has obtained 787 invention patent approvals, 25 utility model patents and 92 apparel design patents.

Prospects
The COVID-19 pandemic remains serious in regions outside China, which will continue to affect the economy. Through implementing effective prevention and control measures, the pandemic in China has essentially come under control and enterprises around the country have gradually resumed work and operation. The decline in economic indicators has also narrowed. Hence, China is expected to be among the first countries to leave the worst impact of the pandemic behind and return to normal production, everyday life and routine medical procedures. Pent-up demand for medical diagnosis and treatment limited by isolation during the pandemic period will gradually be unleashed, which might lead to the rapid growth for the pharmaceutical industry in the immediate future.

The nationwide implementation and extension of the centralized drug procurement programme in “4+7” cities has substantially squeezed the profit of selected drugs as well as many competitive generic drugs. The COVID-19 pandemic has weighed further on the operations of small- and medium-pharmaceutical companies with limited R&D capabilities and only a few new products. Some of them are even encountering difficulties in maintaining the viability of their business. As a result, the consolidation and elimination of the weaker players in the market will accelerate and developing and launching innovative and popular products have become the primary capabilities required by pharmaceutical enterprises if they wish to win amidst the fiercer market competition.

The Group’s strong investment in R&D over the years has borne fruit, as evidenced by the maturing innovative platforms and optimization of creative talent structure for both small molecule and macro-molecule drugs. The continuous huge investment in R&D has also ensured that it can engage in the launch of new products every year, which has become and will continue to be the key growth driver for the Group’s results.

Introduction of Newly Approved Products:
Tianqingsuchang (Budesonide Suspension for Inhalation): A glucocorticoid inhalant with strong anti-inflammatory properties used for first-line treatment of asthma. There are approximately 235 million asthma patients globally, and the number in China exceeds 45 million. The efficacy of nebulized inhalation suspension is more trusted by doctors and patients when compared to other dosage forms but needs to be administered under the supervision of medical professionals in hospitals.

Sitagliptin Phosphate Tablet: An effective and highly selective dipeptidyl peptidase-4 (DPP-4) inhibitor used for improving glycemic control in patients with type 2 diabetes mellitus. Clinical trials show its efficacy in lowering blood sugar, and it can be used alone with high safety and fair tolerance, without increasing the risk of hypoglycemia and causing gastrointestinal reactions. More importantly, it offers long-term protection of beta-cells in the pancreas, which can slow the progress of diabetes.

Dabigatran Etexilate Capsules: A new generation non-Vitamin K oral anticoagulant used for the prevention of stroke and systemic embolism in patients with non-valvular atrial fibrillation. It is the first new oral anticoagulant launched since Warfarin in 50 years, and is the first oral anticoagulant approved for long term indications, signifying a milestone in the global anticoagulant drug sector.

About Sino Biopharmaceutical Limited (HKEX:1177)
Sino Biopharmaceutical Limited is a leading, innovative R&D driven pharmaceutical conglomerate in the PRC. Its business encompasses a fully-integrated chain which covers an array of R&D platforms, a line-up of intelligent production and a strong sales system. The Group’s products have gained a competitive foothold in various therapeutic categories with promising potentials, comprising a variety of biopharmaceutical and chemical medicines for treating tumors, liver diseases, respiratory system diseases, anti-infectious diseases and orthopedic diseases.

Sino Biopharm is a constituent stock of the following indices: MSCI Global Standard Indices – MSCI China Index, Hang Seng Index, Hang Seng Index – Commerce & Industry, Hang Seng Composite Index, Hang Seng Composite Industry Index – Consumer Goods, Hang Seng Composite LargeCap Index, Hang Seng Composite LargeCap & MidCap Index, Hang Seng China (Hong Kong-listed) 100 Index and Hang Seng Stock Connect Hong Kong Index. Sino Biopharm was ranked as one of “Asia’s Fab 50 Companies” by Forbes Asia for three consecutive years in 2016, 2017 and 2018.

New Drug Application of Penpulimab Co-developed by Sino Biopharmaceutical and Akeso Accepted by the National Medical Products Administration

Sino Biopharmaceutical Limited (HKEX: 1177), a leading, innovative R&D driven pharmaceutical conglomerate in the PRC, has announced that the new drug application of the anti PD-1 monoclonal antibody drug (generic name: Penpulimab; R&D code: AK105) jointly developed and commercialized with Akeso, Inc. (HKEX: 9926), a biopharmaceutical company committed to R&D, production and commercialization of affordable innovative antibody drugs for patients worldwide, has been accepted by the National Medical Products Administration of the PRC, for the treatment of patients with relapsed or refractory Classical Hodgkin’s Lymphoma.

Classical Hodgkin Lymphoma (cHL) is a B-cell lymphoma, and is also one of the most common malignancies among young people. It has a single modal age distribution in China with a peak at around 40 years of age . cHL is one of the few tumors that can be cured, and the most common therapy is chemotherapy plus radiotherapy, with the 5-year survival rate of patients as high as over 80%. Although the first-line chemotherapy has a high clinical cure rate, a considerable portion of patients are insensitive to chemotherapy and approximately 5% to 10% of patients do not respond to the initial treatment .

Professor Zhu Jun, Co-principal investigator of the lead unit Beijing Cancer Hospital is full of expectations for such a differentiated anti PD-1 monoclonal product and said, through bioengineering technology, Penpulimab completely eliminate the binding activity of Fc receptors and avoid the antibody-dependent cell-mediated cytotoxicity (ADCC) effect. At the same time, compared with other drugs available in the market working on the same target, it has a slower rate of antigen binding and dissociation, which makes the biological effect stronger and improves its anti-tumor activity.

Co-lead researcher Professor Song Yuqin, Director of Lymphoma Department at Peking University Cancer Hospital said, in clinical trial, Penpulimab was observed with gratifying therapeutic data and good safety. As a clinician, Professor Song hoped that Penpulimab can be launched to the market soon, which will benefit more patients and their families.

About Sino Biopharmaceutical Limited (HKEX: 1177)
Sino Biopharmaceutical Limited is a leading, innovative R&D driven pharmaceutical conglomerate in the PRC. Its business encompasses a fully-integrated chain which covers an array of R&D platforms, a line-up of intelligent production and a strong sales system. The Group’s products have gained a competitive foothold in various therapeutic categories with promising potentials, comprising a variety of biopharmaceutical and chemical medicines for treating tumors, liver diseases, respiratory system diseases, anti-infectious diseases and orthopedic diseases.

Sino Biopharm is a constituent stock of the following indices: MSCI Global Standard Indices – MSCI China Index, Hang Seng Index, Hang Seng Index – Commerce & Industry, Hang Seng Composite Index, Hang Seng Composite Industry Index – Consumer Goods, Hang Seng Composite LargeCap Index, Hang Seng Composite LargeCap & MidCap Index, Hang Seng China (Hong Kong-listed) 100 Index and Hang Seng Stock Connect Hong Kong Index. Sino Biopharm was ranked as one of “Asia’s Fab 50 Companies” by Forbes Asia for three consecutive years in 2016, 2017 and 2018. http://www.sinobiopharm.com/.

Results from Clinical Trials of Penpulimab in Combination with Anlotinib for 1L HCC Co-developed by Sino Biopharmaceutical and Akeso Accepted for Presentation at ASCO Annual Meeting

Sino Biopharmaceutical Limited (HKEX: 1177), a leading, innovative research and development (“R&D”) driven pharmaceutical conglomerate in the PRC, has announced that the abstracts on phase II study on clinical efficacy and safety of Penpulimab (AK105, PD-1 monoclonal antibody) it jointly developed and commercialized with Akeso, Inc. (“Akeso”, HKEX:9926) in combination with Anlotinib for first-line treatment of advanced hepatocellular carcinoma (“1L HCC”), have been accepted for poster presentation at the upcoming 2020 American Society of Clinical Oncology (“ASCO”) Annual Meeting.

As of to date, various phase II/III studies on combination of Penpulimab with Anlotinib have been activated, regarding treatment of various major tumors including: squamous non-small cell lung cancer, gastric cancer, esophageal squamous cell carcinoma, HCC, urothelial cancer, head and neck cancer, MSI-H or dMMR solid tumor and neuroendocrine carcinoma.

Prof. Shunchang Jiao, Director of Oncology Department of General Hospital of People’s Liberation Army, also the leading Principal Investigator for this study, said, “The current option for treating unresectable HCC are mainly sorafenib and recently approved lenvatinib. The overall survival for levatinib was similar to that of sorafenib and the overall survival rate at 6 months for sorafenib was 72.2% . Anti-PD-1 Penpulimab in combination with lower dose of anti-angiogenic inhibitor Anlotinib shows encouraging early efficacy results and good safety profile for unresectable HCC. The DCR reached 84% and the overall survival rate at 6 months reached 91.6% which apparently was a great improvement on clinical efficacy. This combination therapy had a manageable safety profile, and had a potential safety advantage as compared with other combination therapies of immunotherapy and anti-angiogenic inhibitor. The preliminary results from this study suggest that Penpulimab with higher dose of Anlotinib may further improve the clinical efficacy for unresectable HCC patients. As a clinician, I look forward to bringing better treatment options for HCC patients in the near future.”

Dr. Jia Fan, Academician, Director of Fudan University affiliated Zhongshan Hospital, said, “Clinical results from a phase II study of anti-PD-1 Penpulimab in combination with anti-angiogenic inhibitor Anlotinib as first-line therapy for unresectable HCC to be released on the coming ASCO20 show that the combination therapy had a manageable safety profile and encouraging antitumor activities. Based on the preliminary data of this study, the evaluation of Penpulimab in combination with Anlotinib in a phase III study for first-line HCC versus sorafenib is currently underway. Co-leading sites Fudan University affiliated Zhongshan Hospital and General Hospital of People’s Liberation Army along with more than 60 other sites across the country participated in this study.

HCC, one of the most dominating malignant tumors in China, a barricade to invade, still needs more efforts on diagnosis and treatment. The rise of China-based innovative drug discovery and development is strongly promoting the continuous advances in HCC treatment in China. The combination therapy of Penpulimab, an anti-PD-1 antibody with key differentiating features, and the novel small molecule anti-angiogenic inhibitor of multi-targets Anlotinib is expected to become one of the essential first-line treatment options for HCC.”

Akeso is a biopharmaceutical company committed to R&D, production and commercialization of affordable innovative antibody drugs for patients worldwide. The ASCO Annual Meeting is one of the largest and most authoritative clinical oncology conferences in the world where top oncology experts worldwide gather to discuss the results of recent clinical oncology studies and the latest oncology treatment technologies. Many of these professionals select this conference to first announce important discoveries and clinical trial results.

About Sino Biopharmaceutical Limited (HKEX:1177)
Sino Biopharmaceutical Limited is a leading, innovative R&D driven pharmaceutical conglomerate in the PRC. Its business encompasses a fully-integrated chain which covers an array of R&D platforms, a line-up of intelligent production and a strong sales system. The Group’s products have gained a competitive foothold in various therapeutic categories with promising potentials, comprising a variety of biopharmaceutical and chemical medicines for treating liver diseases, tumors, cardio-cerebral diseases, orthopedic diseases, digestive system diseases, infections and respiratory system diseases.

Sino Biopharm is a constituent stock of the following indices: MSCI Global Standard Indices – MSCI China Index, Hang Seng Index, Hang Seng Index – Commerce & Industry, Hang Seng Composite Index, Hang Seng Composite Industry Index – Consumer Goods, Hang Seng Composite LargeCap Index, Hang Seng Composite LargeCap & MidCap Index, Hang Seng China (Hong Kong-listed) 100 Index and Hang Seng Stock Connect Hong Kong Index. Sino Biopharm was ranked as one of “Asia’s Fab 50 Companies” by Forbes Asia for three consecutive years in 2016, 2017 and 2018.

Sino Biopharmaceutical Announces 2019 Third Quarterly Results

Sino Biopharmaceutical Limited (“Sino Biopharmaceutical” or the “Company”, together with its subsidiaries, the “Group”) (HKEX:1177), a leading and innovation-driven pharmaceutical conglomerate in the PRC, has announced its unaudited third quarterly results for the nine months ended 30 September 2019 (“the review period”).

Results Highlights
– The Group’s major product Anlotinib obtained approval for a new indication for the treatment of small cell lung cancer.
– Important overseas registration made: the United States Food and Drug Administration (“FDA”) approved abbreviated new drug application (“ANDA”) for Ticagrelor Tablet.
– Production approval secured for 8 drugs with strong growth potential: the first line or second line prostate cancer drug Abiraterone Acetate Tablet, 3 specifications for new indications of Anlotinib Hydrochloride Capsules, Rivaroxaban Tablets, Tofacitinib Citrate Tablets (a new oral Janus kinase (JAK) inhibitor for rheumatoid arthritis treatment), Azacitidine for Injection and Moxifloxacin Hydrochloride Injection.
– Sales of new products accounted for approximately 20.6% of the Group’s total revenue.
– Subsidiary companies CT Tianqing ranked 16th and Beijing Tide ranked 41st among the “2018 Top 100 Pharmaceutical Companies in China” announced at the “2019 (36th) National Pharmaceutical Industry Annual Information Conference”.
– CT Tianqing and Akeso Biopharma signed a joint venture contract to set up Chia Tai Tianqing Akeso (Shanghai) Biomedical Technology Company Limited in Shanghai. The two parties will cooperate on pursuing development of the tumor immunotherapy PD-1 antibody drug (AK105 Project), which has apparent differentiated advantages.
– CT Tianqing ranked 26th among the “Top 500 Chinese Enterprises with the Most Patents” announced at the “2019 China Marketing International Conference and China Creation Forum”.
– Sino Biopharm ranked 1st among the “Top 20 Competitive Chinese Listed Pharmaceutical Companies in 2019” and also ranked 2nd of First Tier of “Top 100 Chinese Innovative Pharmaceutical Enterprises”, awarded jointly by China Pharmaceutical Enterprises Association and China Medicinal Biotech Association.

Results
For the nine months ended 30 September 2019, the Group recorded revenue of approximately RMB19,321 million, representing an increase of approximately 22.8% over the same period last year. During the period, profit attributable to the owners of the parent was approximately RMB2,256 million, approximately 2.5% higher than that of the same period last year. Excluding the impact of the amortization expenses of new identifiable intangible assets arising from the acquisition of 24% interests in Beijing Tide, as well as the unrealized fair value losses on equity investments and financials assets, underlying profit attributable to owners of the parent amounted to approximately RMB2,600 million, surging by approximately 15.7% as compared with the same period last year. Based on underlying profit attributable to the owners of the parent, the earnings per share were approximately RMB20.65 cents, 14.0% higher than that of the same period last year. The Group has maintained a strong financial position with cash and bank balances reaching approximately RMB6,136 million at the period end.

The Board of Directors declared a quarterly dividend of HK2 cents per share. Together with the first quarterly dividend of HK2 cents per share and the second quarterly dividend of HK2 cents paid, the total dividend of the three quarters amounted to HK6 cents per share.

Business Highlights
During the review period, the Group’s self-developed heavyweight medicine Anlotinib managed greater academic influence thus maintained high growth. The strong academic influence also translated into a strong boost of the results of other oncology products including Shoufu, Yinishu, Saiweijian and Qianping. The chronic disease management model combined with market penetration strategy saw drugs which have passed Consistency Evaluation such as Yilunping and Tuotuo boost the performance of other cardio-cerebral drugs such as Kaina and Xijia. Digestive system medicines such as Aisuping, Deyou and Getai, respiratory system medicines such as Tianqingsule and Zhongchang, hepatitis medicine Ganping, anti-infectious medicines Tianjie and Tianli, orthopedic medicine Yigu, and diabetic medicine Taibai all performed satisfactorily. With a portfolio of growth products more diverse and balanced in terms of revenue contribution, risk resistance of the Group has been strengthened.

On the R&D front, the Group boasted fruitful results. During the third quarter, the Group obtained 8 production approvals and had 6 products passed Consistency Evaluation, including Abiraterone Acetate Tablet (deemed), Metformin Hydrochloride Extended-Release Tablets (deemed), Rivaroxaban Tablets (deemed), Imatinib Mesylate Capsules, Tofacitinib Citrate Tablets (deemed) and Azacitidine for Injection (deemed). It also obtained 5 clinical trial approvals, and submitted 8 Consistency Evaluation applications and 5 clinical trial applications for new Category I medicines, all accepted for review. In addition, the Group was granted 27 invention patents and filed 91 applications for invention patents.

During the review period, the sales performance of the Group’s major medicine categories are outlined below:

Hepatitis medicines
– The sales of hepatitis medicines amounted to approximately RMB4,966 million, representing approximately 25.7% of the Group’s revenue.
Tianqingganping enteric capsules sales amounted to approximately RMB421 million, an increase of approximately 27.7% against the same period last year.
Tianqingganmei injections recorded sales of approximately RMB1,480 million, an increase of approximately 10.2% against the same period last year.
Runzhong dispersible tablet sales amounted to approximately RMB2,335 million.
Sales of Ganze capsules amounted to approximately RMB115 million, an increase of approximately 5.3% against the same period last year.

Oncology medicines
– The sales of oncology medicines amounted to approximately RMB4,202 million, representing approximately 21.8% of the Group’s revenue.
Sales of Saiweijian injections amounted to approximately RMB543 million during the review period, an increase of approximately 39.9% as compared with the same period last year.
Sales of Tianqingyitai injections amounted to approximately RMB170 million, an increase of approximately 4.3% as compared with the same period last year.
Sales of Qingweike injections amounted to approximately RMB168 million.
Sales of Yinishu tablets amounted to approximately RMB182 million, a significant increase of approximately 47.6% as compared with the same period last year.
Sales of Shoufu tablets amounted to approximately RMB173 million, an increase of 29.8% as compared with the same period last year.
Sales of Genike capsules amounted to approximately RMB160 million.
Sales of new product Anxian capsules amounted to approximately RMB137 million.
Sales of another new product Qianping injections amounted to approximately RMB128 million, a sharp increase of 211.6% as compared with the same period last year.

Cardio-cerebral medicines
– The sales of cardio-cerebral medicines amounted to approximately RMB2,495 million, representing approximately 12.9% of the Group’s revenue.
Tianqingning injections recorded sales of approximately RMB113 million.
Sales of Yilunping tablets amounted to approximately RMB734 million, a year-on-year increase of approximately 20.8%.
Sales of Tuotuo calcium tablets amounted to approximately RMB613 million, a year-on-year increase of approximately 23.6%.
Sales of Kaishi injections amounted to approximately RMB504 million.
Sales of Kaina tablets amounted to approximately RMB372 million, an increase of approximately 22.7% as compared with the same period last year.

Analgesic medicines
– The sales of analgesic medicines amounted to approximately RMB1,653 million, representing approximately 8.6% of the Group’s revenue.
Sales of Kaifen injections amounted to approximately RMB919 million.
Sales of Debaian Cataplasm amounted to approximately RMB717 million, approximately 41.5% higher than that of the same period last year.

Orthopedic medicines
– The sales of orthopedic medicines amounted to approximately RMB1,406 million, representing approximately 7.3% of the Group’s revenue.
Sales of Gaisanchun capsules amounted to approximately RMB820 million, rising by approximately 5.2% as compared with the same period last year.
Sales of Jiuli tablets amounted to approximately RMB290 million, an increase of approximately 31.3% against the same period last year.
Sales of Yigu injections amounted to approximately RMB247 million, a remarkable increase of approximately 77.3% against the same period last year.

Digestive system medicines
– The sales of digestive system medicines amounted to approximately RMB1,194 million, representing approximately 6.2% of the Group’s revenue.
Sales of Getai tablets amounted to approximately RMB227 million, an increase of approximately 21.3% as compared with the same period last year.
Sales of Aisuping injection amounted to approximately RMB776 million, a significant increase of approximately 35.1% as compared with the same period last year.
Sales of Deyou granule amounted to approximately RMB134 million, a remarkable increase of approximately 89.3% as compared with the same period last year.

Respiratory system medicines
– The sales of respiratory medicines amounted to approximately RMB843 million, representing approximately 4.4% of the Group’s revenue.
Sales of Tianqingsule inhalation powder amounted to approximately RMB502 million, an increase of approximately 30.7% as compared with the same period last year.
Sales of Chia Tai Suke tablets amounted to approximately RMB181 million, an increase of approximately 17.6% as compared with the same period last year.
Sales of Zhongchang tablets amounted to approximately RMB121 million, a significant increase of approximately 102.3% as compared with the same period last year.

Anti-infectious medicines
– The sales of anti-infectious medicines amounted to approximately RMB838 million, representing approximately 4.3% of the Group’s revenue.
Sales of Tiance injections amounted to approximately RMB476 million, an increase of approximately 2.2% against the same period last year.
Sales of Tianjie injections amounted to approximately RMB258 million, an increase of approximately 42.6% against the same period last year.
Sales of Tianli (Linezolid and Glucose) injections amounted to approximately RMB77.88 million, a significant increase of approximately 93.2% against the same period last year.

Parenteral nutritious medicines
– The sales of parenteral medicines amounted to approximately RMB538 million, representing approximately 2.8% of the Group’s revenue.
Sales of Xinhaineng injections amounted to approximately RMB401 million, an increase of approximately 6.2% against the same period last year.
Sales of Fenghaineng fructose injections amounted to approximately RMB127 million.

Diabetic medicines
– The sales of diabetic medicines amounted to approximately RMB122 million, representing approximately 0.6% of the Group’s revenue.
Sales of Taibai sustained release tablets amounted to approximately RMB110 million, an increase of approximately 26.8% as compared with the same period last year.

R&D
The Group has continued to focus its R&D efforts on new hepatitis, oncology, respiratory system, analgesic and cardio-cerebral medicines. During the third quarter, the Group was granted 5 clinical trial approvals, 8 production approvals, and 6 approvals for Consistency Evaluation, and made 5 clinical trial applications, 8 applications for Consistency Evaluation and 4 production applications. Cumulatively, a total of 471 pharmaceutical products had obtained clinical trial approval, or were under clinical trial or applying for production approval. Out of these, 32 were for hepatitis medicines, 199 for oncology and oncology auxiliary medicines, 27 for respiratory system medicines, 26 for endocrine, 47 for cardiocerebral medicines and 140 for other medicines.

Over the years, the Group has been placing high importance on R&D and innovation, as well as through collaboration and imitation, to raise both R&D standards and efficiency. In light of the fact that R&D continues to be the lifeblood of the Group’s development, the Group continues to devote into more resources. For the nine months ended 30 September, 2019, the R&D expenditure of approximately RMB2,054 million, which accounted for approximately 10.6% of the Group’s revenue, was charged to the statement of profit or loss.

The Group also emphasizes on the protection of intellectual property rights. It encourages its enterprises to apply for patent applications as a means to enhance the Group’s core competitiveness. During the third quarter, the Group has received 35 authorized patent notices (27 invention patents and 8 apparel design patents) and filed 112 new patent applications (91 invention patents, 5 utility model patents and 16 apparel design patents). Cumulatively, the Group has obtained 743 invention patent approvals, 23 utility model patents and 90 apparel design patents.

Prospects
Looking to the full year, the external environment is still full of uncertainties, however, for the Chinese economy, positive factors supporting its stable growth have increased. The “4+7” cities centralized drug procurement program and the expansion of the trial cities to cover the entire country will affect the revenue and profit of covered drugs, and the category structure and revenue of drugs in the country’s pharmaceutical market will thus change gradually. As such, enterprises, the likes of Sino Biopharmaceutical, which offer high-value innovative products and have raw materials and cost advantages will be able to consolidate their market position.

About Sino Biopharmaceutical Limited (HKEX:1177)
Sino Biopharmaceutical Limited is a leading innovation-driven pharmaceutical conglomerate in the PRC. Its business encompasses a fully-integrated chain which spans from R&D to the manufacture and sales of pharmaceutical products. The Group’s products have gained a competitive foothold across various therapeutic categories with promising potential, covering a vast array of biopharmaceutical and chemical medicines for treating tumors, liver diseases, respiratory system diseases, analgesia, cardio-cerebral diseases and orthopedic diseases.

Sino Biopharmaceutical is a constituent stock of the following indices: MSCI Global Standard Indices – MSCI China Index, Hang Seng Index, Hang Seng Index – Commerce & Industry, Hang Seng Composite Index, Hang Seng Composite Industry Index – Consumer Goods, Hang Seng Composite LargeCap Index, Hang Seng Composite LargeCap & MidCap Index, Hang Seng China (Hong Kong-listed) 100 Index and Hang Seng Stock Connect Hong Kong Index. Sino Biopharmaceutical was ranked as one of “Asia’s Fab 50 Companies” by Forbes Asia for three consecutive years in 2016, 2017 and 2018.