Yantai, China, May 4, 2023 – Boan Biotech，a subsidiary of Luye Pharma Group, today announced that an international multi-center Phase 3 clinical study for its in-house developed Denosumab Injection (BA6101; BA1102) has been initiated in Europe, the United States, and Japan, and recently the first patient in (FPI) was achieved.
BA6101 and BA1102 are biosimilar products to Prolia® and Xgeva®, respectively. Prolia® has been approved worldwide for the following indications: 1. Treatment of postmenopausal women with osteoporosis at high risk for fracture. In postmenopausal women, Prolia® significantly reduces the risk of vertebral, non-vertebral, and hip fractures; 2. Treatment to increase bone mass in men with osteoporosis at high risk for fracture; 3. Treatment of glucocorticoid-induced osteoporosis in men and women at high risk for fracture; 4. Treatment to increase bone mass in men at high risk for fracture receiving androgen deprivation therapy for nonmetastatic prostate cancer; 5. Treatment to increase bone mass in women at high risk for fracture receiving adjuvant aromatase inhibitor therapy for breast cancer. Xgeva® has been approved worldwide for the following indications: 1. Prevention of skeletal-related events in patients with bone metastases from solid tumors; 2. Treatment of adults and skeletally mature adolescents with giant cell tumor of bone that is unresectable or where surgical resection is likely to result in severe morbidity; 3. Treatment of hypercalcemia of malignancy refractory to bisphosphonate therapy.
This international multi-center Phase 3 study is a randomized, double-blind, parallel-group, reference-controlled comparative study to evaluate the efficacy, safety, pharmacokinetics, and immunogenicity of Boan Biotech’s biosimilar product compared with the reference product. According to the Guidance for Industry Scientific Considerations in Demonstrating Biosimilarity to a Reference Product1 issued by FDA, the Guideline on similar biological medicinal products2 issued by EMA, the Guideline for the Quality, Safety, and Efficacy Assurance of Follow-on Biologics3 issued by PMDA and based on the discussion with FDA, EMA and PMDA, after completion of the Phase 3 clinical study, BA6101 and BA1102 can apply and be approved for all same indications as Prolia® and Xgeva® in Europe, the United States, and Japan.
Previously, BA6101 (Boyoubei®) was approved for marketing in China in November 2022, as the first approved Prolia® biosimilar in the world. The product was awarded “Top 10 Biopharmaceutical Advancements in China” and the results of the two Phase 1 clinical studies of Boyoubei® were published in Expert Opinion on Investigational Drugs4 and Frontiers in Pharmacology5, respectively. Additionally, Boyoubei®’s Phase 3 clinical study was published in Journal of Orthopaedic Translation6. BA1102's Biologics License Application (BLA) was also accepted by the Center for Drug Evaluation of the National Medical Products Administration of China in March 2023.
Based on the huge patient demand and proven clinical value of the drug, Boan Biotech believes that denosumab presents a broad market prospect on a global scale. According to public available data, Prolia® and Xgeva® had global sales of $3.63 billion and $2.01 billion respectively in 2022.
Dr. Dou Changlin, President of R&D and Chief Operating Officer of Boan Biotech, said: “At Boan Biotech, we’re committed to serving patients around the world with high-quality biologics. BA6101 and BA1102 are in-house developed by the company in accordance with the regulations of China, the United States, the European Union and Japan. The initiation of the international Phase 3 clinical trial is another milestone for Boan Biotech to seek global development. We will accelerate the clinical development of these two products as well as the strategic planning for the subsequent introduction of more biologics into the global markets in order to build a leading Chinese biopharmaceutical brand around the world.”
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About Boan Biotech
As a subsidiary of Luye Pharma Group, Boan Biotech (6955.HK) is a fully-integrated biopharmaceutical company developing, manufacturing, and marketing biologics, with a focus on oncology, autoimmune diseases, ophthalmology, and metabolic diseases. The company discovers antibodies on three technology platforms: Human Antibody Transgenic Mouse and Phage Display Technology Platform, Bispecific T-cell Engager Technology Platform, and ADC Technology Platform. Boan Biotech operates across the entire value chain of the industry from antibody discovery, cell line development, upstream and downstream process development, analytical and bio-analytical method development, and technology transfer to pilot and commercial production.
Boan Biotech’s portfolio includes two commercial products. Its pipeline includes multiple innovative antibodies as drug candidates protected for their international intellectual property rights and a number of biosimilar candidates. In addition to China, the company is also developing biopharmaceutical products in overseas markets, including the U.S. and the EU. With a differentiated portfolio and well-established commercial capabilities, Boan Biotech operates across the industry' s value chain from research and development to manufacturing and commercialization. This has laid a solid foundation for its long-term, high-quality growth.
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Note: FDA is the US Food and Drug Administration, EMA is the European Medicines Agency, and PMDA is Japanese Pharmaceuticals and Medical Devices Agency
References：
Yantai, China, May 4, 2023 – Boan Biotech，a subsidiary of Luye Pharma Group, today announced that an international multi-center Phase 3 clinical study for its in-house developed Denosumab Injection (BA6101; BA1102) has been initiated in Europe, the United States, and Japan, and recently the first patient in (FPI) was achieved.
BA6101 and BA1102 are biosimilar products to Prolia® and Xgeva®, respectively. Prolia® has been approved worldwide for the following indications: 1. Treatment of postmenopausal women with osteoporosis at high risk for fracture. In postmenopausal women, Prolia® significantly reduces the risk of vertebral, non-vertebral, and hip fractures; 2. Treatment to increase bone mass in men with osteoporosis at high risk for fracture; 3. Treatment of glucocorticoid-induced osteoporosis in men and women at high risk for fracture; 4. Treatment to increase bone mass in men at high risk for fracture receiving androgen deprivation therapy for nonmetastatic prostate cancer; 5. Treatment to increase bone mass in women at high risk for fracture receiving adjuvant aromatase inhibitor therapy for breast cancer. Xgeva® has been approved worldwide for the following indications: 1. Prevention of skeletal-related events in patients with bone metastases from solid tumors; 2. Treatment of adults and skeletally mature adolescents with giant cell tumor of bone that is unresectable or where surgical resection is likely to result in severe morbidity; 3. Treatment of hypercalcemia of malignancy refractory to bisphosphonate therapy.
This international multi-center Phase 3 study is a randomized, double-blind, parallel-group, reference-controlled comparative study to evaluate the efficacy, safety, pharmacokinetics, and immunogenicity of Boan Biotech’s biosimilar product compared with the reference product. According to the Guidance for Industry Scientific Considerations in Demonstrating Biosimilarity to a Reference Product1 issued by FDA, the Guideline on similar biological medicinal products2 issued by EMA, the Guideline for the Quality, Safety, and Efficacy Assurance of Follow-on Biologics3 issued by PMDA and based on the discussion with FDA, EMA and PMDA, after completion of the Phase 3 clinical study, BA6101 and BA1102 can apply and be approved for all same indications as Prolia® and Xgeva® in Europe, the United States, and Japan.
Previously, BA6101 (Boyoubei®) was approved for marketing in China in November 2022, as the first approved Prolia® biosimilar in the world. The product was awarded “Top 10 Biopharmaceutical Advancements in China” and the results of the two Phase 1 clinical studies of Boyoubei® were published in Expert Opinion on Investigational Drugs4 and Frontiers in Pharmacology5, respectively. Additionally, Boyoubei®’s Phase 3 clinical study was published in Journal of Orthopaedic Translation6. BA1102's Biologics License Application (BLA) was also accepted by the Center for Drug Evaluation of the National Medical Products Administration of China in March 2023.
Based on the huge patient demand and proven clinical value of the drug, Boan Biotech believes that denosumab presents a broad market prospect on a global scale. According to public available data, Prolia® and Xgeva® had global sales of $3.63 billion and $2.01 billion respectively in 2022.
Dr. Dou Changlin, President of R&D and Chief Operating Officer of Boan Biotech, said: “At Boan Biotech, we’re committed to serving patients around the world with high-quality biologics. BA6101 and BA1102 are in-house developed by the company in accordance with the regulations of China, the United States, the European Union and Japan. The initiation of the international Phase 3 clinical trial is another milestone for Boan Biotech to seek global development. We will accelerate the clinical development of these two products as well as the strategic planning for the subsequent introduction of more biologics into the global markets in order to build a leading Chinese biopharmaceutical brand around the world.”
###
About Boan Biotech
As a subsidiary of Luye Pharma Group, Boan Biotech (6955.HK) is a fully-integrated biopharmaceutical company developing, manufacturing, and marketing biologics, with a focus on oncology, autoimmune diseases, ophthalmology, and metabolic diseases. The company discovers antibodies on three technology platforms: Human Antibody Transgenic Mouse and Phage Display Technology Platform, Bispecific T-cell Engager Technology Platform, and ADC Technology Platform. Boan Biotech operates across the entire value chain of the industry from antibody discovery, cell line development, upstream and downstream process development, analytical and bio-analytical method development, and technology transfer to pilot and commercial production.
Boan Biotech’s portfolio includes two commercial products. Its pipeline includes multiple innovative antibodies as drug candidates protected for their international intellectual property rights and a number of biosimilar candidates. In addition to China, the company is also developing biopharmaceutical products in overseas markets, including the U.S. and the EU. With a differentiated portfolio and well-established commercial capabilities, Boan Biotech operates across the industry' s value chain from research and development to manufacturing and commercialization. This has laid a solid foundation for its long-term, high-quality growth.
--------------------
Note: FDA is the US Food and Drug Administration, EMA is the European Medicines Agency, and PMDA is Japanese Pharmaceuticals and Medical Devices Agency
References：
