
R&D News
- 2021-10-28
Nature Dialogue with Dr. Aimin Hui: How to Lead R&D of Innovator Drugs?
Chinese pharmaceutical companies are turning their attention to innovation, shifting rapidly from mastery of follow-on drugs to researching first-in-class and best-in-class drugs. Aiming to be a healthcare group with a global presence, Fosun Pharma, established in Shanghai in 1994, has built its core business around innovative drug R&D and manufacturing.
- 2021-10-07
Innovation for Health — The Fourth Hongqiao International Health Technology Innovation Forum Held in Shanghai
On November 6, 2021, as a parallel supporting event of the 4th China International Import Expo (CIIE), the 4th Hongqiao International Health Technology Innovation Forum with the theme of "Innovation for Good Health" was successfully held. This forum was sponsored by the International Health Exchange and Cooperation Center NHC PRC (IHECC) and China Pharmaceutical Innovation and Research Development Association,
- 2021-09-28
2021 CSCO | Henlius Publishes Newest Phase II Clinical Data of Novel Anti-PD-1 mAb Serplulimab for Treatment of Advanced Cervical Cancer
In this meeting, Henlius releases phase 2 study results of serplulimab (HLX10, novel anti-PD-1 antibody), in patients with advanced cervical cancer in an oral presentation.
- 2021-09-28
2021 CSCO | Henlius Publishes Phase III Clinical Data of Bevacizumab Biosimilar HLX04 for Treatment of Metastatic Colorectal Cancer
In this meeting, Henlius releases phase 3 study results of HLX04 (bevacizumab biosimilar), in patients with metastatic colorectal cancer in an oral presentation.
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- 2021-03-18
Fosun Pharma: Approval for Clinical Trial of Small Molecule Innovator Drug for the Treatment of Advanced Solid Tumors
[March 18, 2021 in Shanghai, China] Shanghai Fosun Pharmaceutical (Group) Co., Ltd. ("Fosun Pharma"; stock code: 600196.SH; 02196.HK) announced that its subsidiary YaoPharma Co., Ltd. ("YaoPharma") had recently received the approval from the NMPA regarding the clinical trial for the YP01001 capsules (the “Investigational New Drug”) for the treatment of advanced solid tumors.
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- 2021-02-25
BioNTech and Fosun Pharma Receive Special Import Authorization in Macau for COVID-19 mRNA Vaccine
Macau plans to purchase a total of 400,000 doses (including the 105,000 doses granted the Special Import Authorization) COVID-19 mRNA vaccine BNT162b2 for the local COVID-19 vaccination program.
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- 2021-02-18
Wanbang Biopharma Ticagrelor Tablets and Apixaban Tablets Approved for Marketing
Recently, Jiangsu Wanbang Biopharmaceuticals Co., Ltd. ("Wanbang Biopharma") received marketing approval for Ticagrelor Tablets (Wansujie®) and Apixaban Tablets (Keyue®) from NMPA. The marketing of these two products will help solve more anti-thrombotic needs in clinical practice, benefit more patients, and enrich the product pipeline layout and enhance the product power of Wanbang Biopharma.
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- 2021-02-05
Developments in the Field of Diabetes: Wanbang Biopharma Empagliflozin Approved for Marketing
On February 2, 2021, Wanbang Biopharma's Empagliflozin Tablets, the new generation oral sodium-glucose co-transporter-2 (SGLT2) inhibitor, was approved by NMPA (Approval No.: GYZZ H20213115) for glucose control in patients with type 2 diabetes alone or in combination with metformin or metformin and sulfonylureas.
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- 2021-02-03
New Application of Henlius Bevacizumab — Ophthalmic Indication Receives Clinical Trial Approval In Australia
Shanghai, China, Jan, 29th, 2021 - Shanghai Henlius Biotech, Inc. (2696.HK) announced that the filing of clinical trial for HLX04-O, a recombinant anti-VEGF humanized monoclonal antibody ophthalmic injection, for the treatment of wet age-related macular degeneration (wAMD) has been approved by the Therapeutic Goods Administration, Australia. The Phase 3 clinical study of the project in Australia is intended to be initiated in the near future.
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- 2021-01-25
BioNTech and Fosun Pharma Receive Authorization for Emergency Use of COVID-19 Vaccine in Hong Kong
“We are excited and encouraged that COMIRNATY® has been authorized to emergency use in Hong Kong. This is an important milestone in the joint efforts of BioNTech and Fosun Pharma to achieve vaccine accessibility globally.
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- 2021-01-15
Henlius Reaches Exclusive License Agreement with Chiome for Antibodies Targeting Human TROP2
TROP2 (Trophoblast cell-surface antigen 2) is overexpressed in triple-negative breast cancer, non-small cell lung cancer, urothelial cancer and several other types of solid tumours, potentially to become a druggable target with a broad coverage of different types of tumours in various drug modalities including antibody-drug conjugates (ADC), bispecific antibodies and combination therapies.
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- 2021-01-14
Henlius Daratumumab Biosimilar Receives IND Approval from NMPA
HLX15 is a fully human anti-CD38 IgG1κ monoclonal antibody independently developed by Henlius. On one hand, HLX15 can directly bind to CD38 expressed on the surface of tumor cells, inducing tumor cell lysis and apoptosis through complement-dependent cytotoxicity (CDC), antibody-dependent cell-mediated cytotoxicity (ADCC) and antibody-dependent cellular phagocytosis (ADCP),
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- 2020-12-31
Annual Report | Independent Innovation for Ambitious Progress — Major Achievements in 2020
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