Uni-Bio Science Group Limited 2019 Annual Results Turnover Increased by 54.9% YoY to HK$209.4 Million Recording EBITDA of HK$28.4 Million Achieved Significant Progress Towards Pipeline Product with 2 Product Launches Expected in 2020

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HONG KONG / ACCESSWIRE / March 31, 2020 / A fully integrated biopharmaceutical company - Uni-Bio Science Group Limited ("Uni-Bio Science", together with its subsidiaries referred to as the "Group", stock code: 0690.HK), is pleased to announce its annual results for the year ended 31 December 2019 (the "Year"), as well as its comparatively figures for the year ended 31 December 2018 ("2018").

Key Accomplishments in 2019

During the Year, the Group has recorded a spectrum of accomplishments both in terms of marketed products, and consolidation of the Group's assets. The key highlights include:

  1. GeneTime(R) (EGF spray indicated for wound healing) recorded significant growth with turnover increase by 103.2% year-on-year ("YoY") to approximately HK$128.0 million in 2019. This was mainly attributed to the effective adjustment in marketing strategy. The Group has initiated two new research projects in November 2019 on this product line, aiming to expand its application to new patient groups.

  2. The Group signed a letter of intent with Kai Ping Shi Jian Bao Zhen Tourism Development Company Limited (開平時間寶鎮旅遊發展有限公司) to co-construct and co-operate the healthcare facilities used for chronic disease management in the Greater Bay Area. The agreement is expected to directly benefit the long-term sales of the Group's chronic disease products, especially the soon-to-be-launched rhExendin-4 ("Uni-E4") and rhPTH (1-34) ("Uni-PTH") used in the treatment of diabetes and osteoporosis, respectively.

  3. The Group's Uni-PTH (Teriparatide) high-precision industrialization project was approved by Zhongguancun Science Park Management Committee, showcasing its clinical significance and commercial potential. Upon approval, the Group has received the first installment of government support funds (RMB 10 million) in April 2019, which will be used to support the optimization and upgrades of the production line, the protection of independent intellectual property rights and major core technologies, as well as market promotion in order to prepare for its official launch.

  4. The Group had successfully completed a private placement of HK$30 million of new shares to a new strategic investor - CHMT Peaceful Development Fund Management Limited, which is a multi-strategy fund with worldwide investments in both private and public markets with an asset under management (AUM) of more than USD 5 billion. The proceeds from the placement will be used as the initial capital to progress three new corporate development projects towards the next stage, with hopes to further strengthen the Group's portfolio coverage.

  5. Triazole, recombinant human epidermal growth factor, along with glinides class products of the Group, were once again included in the National Medical Insurance Cataloguein 2019. This has further demonstrated that the market potential of the major products sold by the Group, namely GeneTime(R) (a patented biopharmaceutical recombinant human epidermal growth factor external solution (I)), Pinup(R) (Voriconazole Tablet, a patented chemical) and Bokangtai(R) (Mitiglinide calcium tablets). The Group is expecting a significant and sustainable growth of the above products in the near future.

  6. The Group has completed all consistency assessment experiences for Pinup(R) (Voriconazole oral tablet), a major drug for the treatment of severe fungal infections. Documents has been submitted to the National Medical Products Administration ("NMPA") in August 2019. The Group expects to obtain the consistency assessment certification in the second half of 2020. By completing the consistency assessment, the Group will be in a good position to enter into the centralized drug procurement list and compete against peers who have also passed the consistency assessment.

  7. Uni-PTH, the only anabolic agent effective in improving bone density and reducing the chance of vertebral and hip fractures, is getting a step closer towards its official launch. In December 2019, the Group submitted supplementary drug information to the Center for Drug Evaluation ("CDE"), and the Uni-PTH lyophilized powder injection was expected to be launched in the second half of 2020 after obtaining the drug registration approval.

  8. The NMPA has officially accepted the Group's application for registering Boshutai(R) (Acarbose tablet) as a Category IV chemical drugs in January 2019. The Group is now preparing the submission of supplementary information and expects to obtain the drug registration approval number in the second half of 2020. To enhance competitive advantages, the Group further optimize its cost structure through internal control and external partnership, as the leaner cost structure should in turn offer the Group better positions in market penetration to boost marketing share with limited marketing input.

  9. Uni-E4, an innovative biologic drug self-developed by the Group, is a class of anti-diabetic treatments called GLP-1 agonists and a non-insulin treatment candidate that stimulates the incretin pathway. It is the first fully biologically expressed GLP-1 agent in the world. With its unique biological expression manufacturing process along with its advantages in costs and price, Uni-E4 has the potential of becoming a leading competitor of the GLP1 drugs in the blue ocean market of China. The project is currently under development as scheduled. The CDE has accepted the Group's application for bridging trial of the new Uni-E4 pen injection formulation in December 2019. The Group expects the bridging clinical research of the Uni-E4 injection to begin in 2020, and the drug will be launched after the completion of registration with the NMPA as soon as 2022.