Mira Life Science Ventures United States

Mira Life Science Ventures was established to change the paradigm for investment, incubation and development of new disruptive and game-changing technologies in the life sciences. Mira LSV will invest in medical devices, therapeutics, diagnostics, enabling technologies and digital healthcare. Mira LSV will focus its efforts in areas of significant unmet medical needs such as cancer, neurological diseases, infectious disease, autoimmune disease, inflammatory diseases, personalized medicine, cardiovascular disease and renal diseases.

In order to change the venture investment paradigm, Mira LSV was formed to break out of the traditional venture model and move to a more flexible, nimble and shareholder-centric model to accelerate development of these break-through products and technologies and bring them to patients. Mira LSV’s highly flexible business structure, broad and diverse access to deal-flow and highly experienced management team will ensure we have a significant positive impact on our healthcare system.

Mr. Mel Rothberg
Chairman 
Functionality

MSQ Ventures United States

MSQ Ventures is a New York-based cross-border advisory firm that bridges the healthcare industries globally by offering our deep knowledge, strong network, and local insights into the China market. We provide comprehensive advisory services for our clients’ cross-border projects: market assessment, in/out-licensing, joint ventures, and PR&IR. We currently have offices in New York (headquarter), Beijing, Shanghai, and Shenzhen.
Mr. Estigarribia Marc
MD 

Pfizer China

Pfizer Inc. is an American multinational pharmaceutical corporation. One of the world's largest pharmaceutical companies.
Company Size (Fulltime employees)
Please specify your partnering goal
Looking for innovative products and companies with innovative pipeline assets.
Headquartner in China
Biotech/Pharma Category
Dr. Feng Bian
Dr. Feng Bian
Sr Director/Emerging Science Lead-China 
林 王
医学经理 
Ms. ying wu
Manager 
Functionality
Dr. Ying Niu
China Search and Evaluation Lead 
Functionality

Qilu Pharmaceutical North America China

Located in Jinan, Qilu Pharmaceutical is one of the leading pharmaceutical companies in China. It focuses on developing, manufacturing and marketing of generic drugs and active pharmaceutical ingredients in the therapeutic areas of Oncology, Cerebrovascular & Cardiovascular, Infections, Psychological&Neurological System, Respiratory System, Ophthalmological Diseases, etc. Qilu has more than 8000 employees, 70% of which have the college degree or above.

Qilu pharmaceutical has always been sticking to the innovative development strategy. Guided by the market demand and the product innovation, Qilu has established extensive cooperation with domestic and foreign partners on a series of R&D projects. Qilu pays high attention to the introduction and cultivation of talents and has built a highly qualified R&D team with professional and efficient R&D capabilities, More than 100 national new drugs have been successfully developed, which constitutes the reasonable production line for the future development of Qilu. A number of technological achievements have obtained the national and provincial scientific & technological progress awards and created good social benefit.

Qilu Pharmaceutical has eight manufacturing sites covering an area of more than 2800,000 ㎡for finished dosage forms, chemical synthesis, genetic-engineering, fermentation, etc. The modern workshops are located in the manufacturing sites where the automatic production lines, key equipments and analytical instruments are imported from the leading suppliers all over the world. Now Qilu Pharmaceutical has been one of the leading global suppliers of Antibiotic APIs and Oncology APIs with huge capacity and good quality.

Qilu pharmaceutical has always been committing itself to providing the high-quality products to the patients and the society. Thanks to the integrated and stringent system of quality control and quality assurance, the company has been the leader of cGMP implementation in China. Its non-sterile APIs (fermentation and chemical synthesis), sterile APIs and comprehensive finished dosages have been respectively approved by USFDA, European Directorate for the Quality of Medicines (EDQM), Therapeutic Goods Administration (TGA) of Australia, Medicines and Healthcare products Regulatory Agency (MHRA) of UK, Medicines Control Council (MCC) of South Africa, and some other national competent authorities.

Qilu Pharmaceutical has an integrated product structure and value chain with over 160 launched products. The company has established a comprehensive domestic and overseas sales network. The global presence has covered North America, Europe, CIS countries, South America, Asia, South Africa and Middle East. The valuable brand of the company has been well built with the quality products and good services.
Dr. Jun Sun
VP, Business Development 
Functionality

Shanghai Henlius Biotech China

Henlius (2696.HK) is a leading biopharmaceutical company in China with the vision to offer high-quality, affordable and innovative biologics for patients worldwide with a focus on oncology and autoimmune diseases. Since its inception in 2010, Henlius has built an integrated and efficient global R&D platform with key facilities in Shanghai, Taipei and California, and commercial office in Frankfurt. The three R&D centers closely collaborate with each other to ensure a highly productive and cost-efficient R&D process.
Starting from biosimilar, Henlius presses forward with novel mAb products and immuno-oncology combination therapies with proprietary anti-PD-1 and PD-L1 mAbs as backbone. Henlius establishes a diversified product pipeline of biosimilars, bio-innovative drugs and combination therapies, and builds an integrated platform covering the whole product lifecycle including R&D, commercial-scale production and commercialization.

Keywords : Cancer, Oncology, Biologics, Biosimilar, BioInnovative, Biobetter, Monoclonal Antibody, Mabs, Tumors, Immuno oncology, PD1, PD-L1, EGFR, VEGF, HER2,
Website:
www.henlius.com
Company Size (Fulltime employees)
Year of foundation
2010
Please specify your partnering goal
In & Out Licensing, Collaboration
Headquartner in China
Mr. Jean-Baptiste Duval
VP International Operations 
Functionality

Shanghai Huaota Biopharmaceutical China

Our company focUnited Statesed on innovative drug discovery,Sticking to indevelop R&D,and we have very robUnited Statest pipeline and flexible bUnited Statesiness model.
Website:
www.huaota.cn
Partnering Objectives
Headquartner in China
吉雄 江
BD 

Shanghai junshi biosciences Co.Ltd. China

Shanghai Junshi
丽君 陈
知识产权总监 

Singh Biotechnology United States

We at Singh Biotechnology (SBT) are interested in meeting with you to exploring possible opportunities for partnering/in-licensing/scientific collaboration.

 

SBT is a start-up biotech company established in 2014. We discover/develop unique and proprietary therapeutic single domain antibodies (sdAbs) for the treatment of a variety of cancers, autoimmune, ophthalmological, and viral diseases by leveraging our propriety novel technology platform. Using this technology platform SBT has been able to generate therapeutic sdAbs that specifically target intracellular molecules of interest that play an important role in the pathogenesis of disease(s). Our lead therapeutic (SBT-100) is a bi-specific sdAbs that specifically targets and inhibits intracellular KRAS and signal transducer and activator of transcription 3 (STAT3) proteins.

Company Size (Fulltime employees)
Year of foundation
2014
Please specify your partnering goal
Raising funds for our lead asset, SBT-100, to complete toxicology studies and then go into phase 1.
Headquartner in China
Biotech/Pharma Category
Assets Information 1
SBT-100 is a monomeric single domain antibody (sdAb) that binds KRAS and STAT3 with nanomolar affinity, inhibits the GTPase activity of KRAS, downregulates P-ERK, inhibits the growth of eleven aggressive human cancer in vitro, and suppresses the growth of human cancers in vivo. SBT-100 is the first sdAb to penetrate the cell membrane and give a therapeutic effect in cancers. It also crosses the blood brain barrier (BBB). Through its anti-STAT3 effects, SBT-100 downregulates the expression of VEGF and PD-L1. The significant suppression of PD-L1 expression caused by SBT-100 emphasizes its immunotherapeutic potential. With our preclinical data, the US FDA has given SBT-100 Orphan Drug Designation for pancreatic cancer and osteosarcoma. In addition, we voluntarily requested a Pre-IND review of our triple negative breast cancer (TNBC) program by the FDA. The Pre-IND briefing packet received a favorable review by the FDA of the TNBC data, our SBT-100 manufacturing process, our proposed IND-enabling toxicology studies in rats and monkeys, and our proposed Phase I studies in patients. All of the patents and technology regarding SBT-100 and our other assets are internal to our company. Nothing has been licensed from an outside entity. The patents for SBT-100 and all our other assets have been approved by the U.S.A., Japan, China, South Korea, Taiwan, Canada, Australia, and every country in Europe. These patents are being processed in every other major country and region in the world.
Biotech/Pharma Asset Stage
Slides Deck
(pdf, 1.52MB)
Ashutosh Parihar
Vice President