Cytovance Biologics United States

Cytovance® Biologics is a leading biopharmaceutical Contract Development and Manufacturing Organization (CDMO) that excels in the rapid and cost-effective development and manufacture of large molecule APIs from both mammalian cell culture and microbial fermentation such as monoclonal antibodies, fragment antibodies, bispecifics, enzymes, fusion proteins, vaccines and other biological products including plasmid DNA and cell-based therapeutics. In addition to our clinical and commercial cGMP API manufacturing services, Cytovance offers well integrated development services supporting the entire product lifecycle including cell line development, cell banking, microbial strain development, process and analytical development, and process characterization. A centralized, responsive program management team coordinates all critical CMC activities for each client program around raw materials management, QC testing, ICH stability studies, and regulatory support. Our 140,000 sq. ft. state-of-the-art facilities in Oklahoma City are designed to meet U.S., EU, and other global regulatory standards.
Company Size (Fulltime employees)
Year of foundation
2005
Partnering Objectives
Please specify your partnering goal
TBD
Headquartner in China
Mr. Matt Delaney
VP of Business Development and Marketing 
Functionality

D3 BIO

Website:
www.d3bio.com
Partnering Objectives
Biotech/Pharma Category
Dr John Jin
Dr John Jin
Co-founder & CBO 
Functionality
John Jin
Co-founder&CBO 

Enzymogen Israel

Enzymogen is a biotechnology company developing cannabinoids in algae as new drug entities.
Main activities:
Development of a platform for producing API cannabinoids based on proprietary technology (not plant extracts);
Develop cannabinoids as drugs for unmet clinical needs.

Company Size (Fulltime employees)
Year of foundation
2018
Please specify your partnering goal
Fundraising; partnering; product co-development
Headquartner in China
Assets Information 1
Enzymogen Ltd|Cannabinoids production in microalgae|CNS diseases, Onclology|US, EU, Can, Jap, Chi
Biotech/Pharma Asset Stage
Slides Deck
(pdf, 145.13KB)
Mr. Meir Azulay
Director 
Functionality

EpicentRx United States

EpicentRx is an immuno-oncology company whose focus is to identify and develop less toxic and more effective immunotherapy-based anti-cancer treatments that are active not only as single agents, but that also sensitize tumors to the cytotoxic effects of chemotherapy, radiation and immune checkpoint blockade. EpicentRx's lead program is among a portfolio of novel dinitroazetidine-based drugs that downregulate CD47 – SIRPα to alter the tumor microenvironment and optimize immune responses as well as normalize the tumor vasculature for better drug and oxygen delivery, and has been tested in several clinical trials including an ongoing Phase 3 study in SCLC. The company is also advancing multiple programs through its smart virus AdAPT platform, including three anti-SARS-CoV-2 vaccines, a TGF-beta "trap" starting Phase 1, and various personalized cancer vaccines that have shown to be effective in both chemotherapy and immune resistant tumors. For more information regarding EpicentRx, go to: http://www.epicentrx.com.

Biotech/Pharma Category
Biotech/Pharma Asset Stage
Henry Han
BD Head 
Functionality

Far East Bio-Tec. Co., Ltd China

FEBICO (Far East Bio-Tec. Co., Ltd.) was established in 1976. We have three main business segments: New Drug Development, Diagnostic Reagents, and Dietary Supplement .
We develop an anti-virus platform, FEM, to develop potential drug candidates.
We focus on developments of botanical drugs and biologics to resolve the unmet medical needs such as inflammation diseases (lung injury, liver inflammation, liver fibrosis), hepatitis B, and herpes.
Website:
www.febico.com
Company Size (Fulltime employees)
Year of foundation
1990
Partnering Objectives
Headquartner in China
Biotech/Pharma Asset Stage
Nick Cheh
Director of BD 
Functionality

Ferro Pharma Germany

Since 1989, at ferropharma we are changing the health care market by cutting value chains to decrease cost of drug development and drug availability.
One of our brand, EMELEMA® - Making Latest Medicine Available – is what we believe in and what drives the best talent from around the globe to join us.  
Our aim is to be known as the company that increases patient access to generic and innovative medicine. We focus on building bridges between markets, stakeholders and patients. Collectively, we believe in finding the most fair, straight and reliable provider for the distribution of Active Pharmaceutical Ingredients (API), Finished Dosage Forms (FDF) and services. Thanks to our dedicated teams in Brazil, China, Germany, India and Malta, we are using manufacturing plants for high quality products, in the most efficient way. We direct our attention on novel delivery systems and the provision of EU registered and manufactured drugs..
We made quality our priority. The EMA, FDA and ANVISA standards for APIs and FDFs are our benchmarks that we fulfill.
We operate worldwide but our core markets are China, Latin America and the European Union.
Company Size (Fulltime employees)
Year of foundation
1989
Headquartner in China
Biotech/Pharma Asset Stage
Medtech Development Stage
Mr. Lin Wayne
Vice President Asia Pacific 
Functionality

GCV Life India

Life science-focused Innovation licensing organizations looking to commercialize global innovations for the Indian and South Asian markets through a unique partnership-led model.
Dr. Chirag Jain
Analyst 
Functionality

Generys United States

A clinical-stage US pharma company with a P2B asset (US FDA IND) targeted for multiple substance use disorders and stressor-related disorders (e.g., PTSD) with unmet medical needs.

Website:
N/A
Biotech/Pharma Category
Biotech/Pharma Asset Stage
Tong Lee
CEO 
Functionality

Genova Inc China

Genova Inc., a bio-pharma company dedicated in the innovation of better protein-drugs for viral diseases, cancer and auto-immune diseases. Novaferon ,the first novel protein drug of Genova, shows antiviral efficacy on viral clearance in a proof of concept randomized clinical trial and approved by Healthcare Canada and PMDA of Japan entering into phase 3 multinational centers clinical trial in last December. We are right looking for strategic parthership with big pharma. Contact: ctxu@genova.cn

Website:
www.genova.cn
Company Size (Fulltime employees)
Year of foundation
2006
Please specify your partnering goal
To work with a reputable pharmaceutical, or medical institute, or government agency, on scientific and business development of Novaferon as an antiviral drug for COVID-19. Cooperating specifically on organizing and managing international clinical trials, laboratory and animal studies for COVID-19. Licensing rights for COVID-19 applications of Novaferon in defined territories, further equity cooperation might be accordingly considered
Headquartner in China
Biotech/Pharma Category
Biotech/Pharma Asset Stage
Mr. Kenneth Xu
Vice President & Corporate Secretary 
Functionality

GenScript United States

GenScript is a global biotech company (Stock Code: 1548. HK) with 4,000 employees worldwide. Founded in 2002, GenScript business encompass four major categories in synthetic biology, protein analysis and purification, biologics development and manufacturing, and cell therapy.
Company Size (Fulltime employees)
Year of foundation
2002
Please specify your partnering goal
We are looking for partnering wtih companies provide platform/tools for protein ananlysis, purificaiton and cell separation.
Headquartner in China
Ms. Hong Qian
Head of Catalog Product Unit 
Functionality
Mr. Paul Kao
Mr. Paul Kao
VP, Business Development, Life Science Group 
Functionality