East Continent

Distributer for pharmaceutical products
Company Size (Fulltime employees)
Year of foundation
5
Please specify your partnering goal
To be an agent in Saudi market
Headquartner in China
Suhail Zimmo
Operations Manager 
Functionality

Enosi Life Sciences United States

Enosi's lead programs involve novel inhibitors of TNF (tumor necrosis factor), which include severe inflammation associated with viral infections, autoimmune disease, fibrotic diseases, Alzheimer’s, cancer and other diseases. The current TNF inhibitors have important “Black Box” warnings for opportunistic infections, cancer, and cardiovascular events, like stroke. Enosi believes our compounds in development will avoid these limitations of current drugs, be more effective, and will allow expansion into many indications/markets that cannot be approached at the present time by current TNF inhibitors because of their side-effects.
Website:
enosi-life.com
Company Size (Fulltime employees)
Year of foundation
2020
Please specify your partnering goal
Collaboration to discover and develop molecules for autoimmune disease and cancer
Headquartner in China
Plan in China
Seek collaborations to jointly develop products in cancer and autoimmune disease.
Biotech/Pharma Asset Stage
Medtech Development Stage
h michael shepard
CSO and CEO 
Functionality

ExoProTher Medical LTD Israel

ExoProTher Medical is an Israeli pre-clinical stage company developing a novel biotherapy for cancer treatment, relevant to all cancers with p53 mutation or inactivation - more than 60% of human cancers. Our technology is unique and disruptive and is fully owned by the company.

The company has been funded by private investors. We are currently working on shaping our next funding round.
Company Size (Fulltime employees)
Year of foundation
2017
Funding Status
Seed round raised in early 2020 from private investors and family offices (international).
Headquartner in China
Plan in China
China is now the second largest pharmaceutical market in the world. China’s oncology market alone represents 37% of all lung cancer, 44% of stomach cancer and 52% of liver cancer patients globally. In addition, Chinese pharma companies are active partners in international development. ExoProTher technology is very relevant and, we believe, very attractive to build such partnership. It may be based on joint development with subsequent licensing of commercial rights for the therapy in China. Another option is establishing a partnership aimed at building a manufacturing facility for our novel therapeutic platform.
Lana Volokh
PhD 
Functionality

Focus-X Therapuetics United States

Focus-X is a preclinical stage biotech company committed to the discovery and development of personalized precision medicine fulfilling the unmet needs in cancer diagnosis and treatment. We are to release the true potential of radioligand therapy by leveraging our world class peptide drug discovery platform and joining force with top radiopharmaceutical partners.
Company Size (Fulltime employees)
Year of foundation
< 1
Please specify your partnering goal
Connection to investors and partners
Funding Status
Seed Round - Pre-A
Headquartner in China
Plan in China
Establish operation after next round finance (Within 2 years)
Biotech/Pharma Asset Stage
Fa Liu
CEO 
Functionality

GATTACO Inc. United States

GattaCo is a Southern California start-up that has developed disruptive new technologies and products solving billion dollar bottlenecks in healthcare. These include its A-PON™ and Pediatric mini-PON™ Kits, which are self-contained, fully-automatic and disposable centrifuge replacement tools. The PON devices are used to extract a precise volume of antibody-rich plasma from a few drops of finger-stick capillary blood so that the plasma can be dispensed into a rapid diagnostic testing platform, such as a rapid COVID-19 antibody test, or into a tube for shipping liquid plasma to a clinical lab for analysis. The mini-PON device eliminates the need for a venipuncture for pediatric blood testing. The availability of liquid plasma for clinical lab processing, collected and processed remotely, greatly simplifies lab workflow compared to dried blood sample processing and provides a more consistent and stable sample for high-sensitivity and high-throughput serological testing. When used in conjunction with rapid antibody tests, the PON devices can provide more consistent, higher-sensitivity and quantitative results compared to the same volume of whole blood, and may allow clinically significant rapid tests to be performed in Point of Care settings.
Company Size (Fulltime employees)
Year of foundation
2018
Please specify your partnering goal
Partnership, collaboration, JV, in-licensing diagnostic technology or OEM
Funding Status
Series A 1Q21
Now raising (In USD)
US$ 10 million
Headquartner in China
Biotech/Pharma Category
Medtech Category
Medtech Information 1, Device Name|Description|Development Stage|Licensed Countries
A-PON(TM) Kit|Home sample collection kit delivering liquid plasma to the lab|commercial|
Medtech Information 2
mini-PON(TM) Kit|Pediatric blood sample collection and processing|under development|
Medtech Development Stage
Michael McNeely
LinkedIn logo Pres/CEO 
Functionality

Genervon Biopharmaceuticals United States

There is a high unmet need for central nervous system (CNS) diseases in the growing aging population. Genervon is bringing GM6, a new clinical-stage drug asset, to regulatory approval and commercialization in China for CNS diseases including Parkinson’s disease (PD), Alzheimer’s disease (AD), amyotrophic lateral sclerosis (ALS), Multiple Sclerosis (MS), and other neurodegenerative diseases. Most clinical trials for drugs developed through the traditional single-target drug approach have failed to treat the complex neurological disorders that involve multiple interrelated pathways. GM6 is neither an antibody nor a single-target agonist or antagonist. It is a pleiotropic regulator which simultaneously regulates multiple pathological pathways. Genervon has validated GM6’s target engagement of multiple targets and druggability. GM6 has been de-risked for toxicity in animal studies and safety in three clinical trials. IND documents filed with the FDA can be used to support regulatory filing in China for clinical trials. Genervon is interested to partner through licensing or merger and acquisition. 
Genervon Biopharmaceuticals discovered an endogenous embryonic-stage regulator, Motoneuronotrophic Factor (MNTF), and developed from it the pleiotropic drug GM6. Chronic inflammation is associated with a broad spectrum of neurodegenerative diseases related to aging. GM6 simultaneously modulates multiple biological mechanisms (MOA) in the CNS and immune system to increase neurogenesis and lower inflammation. The MOAs include oxidative Stress, protein aggregation, kinase dysfunction, cholinergic signaling, extracellular matrix stability, and intrinsic apoptosis. GM6 reduces Beta Amyloid and phosphorylated tau in AD, reduces SOD1 in ALS, and reduces inflammation in animal models. GM6 passes through the blood-brain barrier and has good drug-like properties. GM6 has been studied in a Phase 1 and two Phase 2A trials and was shown to be safe and tolerable with positive clinical outcomes and favorable shifts in biomarkers SOD1, Tau and TDP43 in patients. A complete CMC package is ready for technology transfer.
Website:
www.genervon.com
Company Size (Fulltime employees)
Looking for
Please specify your partnering goal
Genervon is interested to partner through out-licensing or merger and acquisition.
Assets Information 1: Name|Description|Indications|Stage|IP countries
GM6|pleiotropic regulator|ALS|Phase 2/3|USA, China, multiple EP, Japan, CA, Au
Assets Information 2
GM6|pleiotropic regulator|PD, MS, AD|Phase 2|USA, China, multiple EP, Japan, CA, Au
Biotech/Pharma Asset Stage
Slides Deck
(pdf, 2.01MB)
Dorothy Ko
Dorothy Ko
Chief Operating Officer 
Functionality

Generys Biopharmaceuticals United States

A clinical-stage pharma company with a P2B asset targeted
for multiple psychiatric disorders with unmetmedical needs.
The parent company, Generys Therapeutics Corp.
headquartered in Rep. of Korea is a controlled foreign
company (US IRS code).
Website:
N/A
Company Size (Fulltime employees)
Year of foundation
2013
Funding Status
Seeking Phase 2B funding
Headquartner in China
Plan in China
License-out/co-development/joint venture agreements to enter China market.
Biotech/Pharma Category
Biotech/Pharma Asset Stage
Tong Lee
LinkedIn logo CEO 
Functionality

Glenpharma AB Sweden

   Glenpharma AB is a small privately owned research spin-off from Pfizer-Pharmacia, formed in Sweden in 2002 to exploit novel technology patented by its founders. 

We offer patented synergistic combinations of biopolymers for 

a) accelerated repair of acute tendon /ligament injuries in human applications ( such as sprained ligaments / tendons in shoulder, elbow, knee, ankle, etc , in both sports injury scenarios and in the elderly ) , or in veterinary indications (e.g. high performance horses) .  The product accelerates healing at least 3 times faster than the normal healing process. 

b) for prevention of unwanted adhesions between tissues after major thoracic, abdominal , fertility or orthopedic surgery. In studies on prevention of difficult adhesions after cardiac surgery, for example, adhesion scores were < 10% of those in control groups.

c) for effective control of acute pain in advanced joint disease (osteo-arthritis (OA)  .  Clinical documentation in advanced OA indicates that onset of pain relief is much faster and of longer duration than current standards for viscosupplementation. 

Each of the above biopolymer "viscous fluid implants" are also ideal drug delivery media for treatment of ancillary complications.

All component biopolymers are well documented APIs, i.e. without the toxicty and other regulatory issues generally associated with "New Chemical Entities".  Glenpharma´s current patent protection covers most major international markets including USA, Europe and P R China.

Glenpharma is primarily seeking Chinese partners for out-licensing within the fields of orthopedics or major surgery.. If neccessary , we can offer contract-manufacturing options in Europe if not available in China. 

Company Size (Fulltime employees)
Year of foundation
2002
Please specify your partnering goal
To develop and market above projects under exclusive license for China .
Headquartner in China
Assets Information 1: Name|Description|Indications|Stage|IP countries
Patents|Novel formulations of biopolymers for repair of injuries to connective tissue|Injuries involving tendons / ligaments , etc in sports injuries, elderly patients, joint disease ( arthritis ) , major surgery.|USA, Canada, Europe, China, Australia, etc
Biotech/Pharma Asset Stage
Medtech Development Stage
Target Client Type
Pharma / Device companies working with orthopedics or major surgery
Slides Deck
(pdf, 600.02KB)
Senior Scientist Peter Buckley
CEO 
Functionality

GlycoSeLect Ltd Ireland

Our company develops and manufactures technology and applications for glycoprotein separation and analysis. We are focussed on the biopharmaceutical industry. We also have customers in medical diagnostic and cosmetic companies.
Our facility is based on the campus of Dublin City University in Ireland.
We have developed an extensive network of contacts not only customers but also opinion leaders in glybiology.

Website:
GlycoSeLect Ltd
Company Size (Fulltime employees)
Year of foundation
2013
Please specify your partnering goal
Joint venture to develop downstream processing applications
Funding Status
Series A
Now raising (In USD)
900,000
Headquartner in China
Plan in China
Seek local partner to establish glycobiology specialist company supplying better glycoprotein product analysis and manufacturing technology with support for application development.
Biotech/Pharma Category
Assets Information 1: Name|Description|Indications|Stage|IP countries
RPL lectins for glycoprotein product analysis & manufacturing applications|Glycan specific proteins for use in detecting and separating glycoproteins|Product analysis and manufacturing, especially vaccines and mAbs.|Worldwide available
Biotech/Pharma Asset Stage
Slides Deck
(pdf, 164.08KB)
Robert Dunne
CEO 
Functionality

Golden State Green World United States

Golden State Green World LLC, is a CBG Hemp Cultivator, located in Riverside County, California. Our team has ten years of extensive greenhouse design and a diverse growing experience. We apply our grow methodologies and eco-agricultural knowledge to supply the global market with high quality, contaminant-free, organic CBG enriched hemp products. Our vision is to become a global distributor of organic CBG infused products that will provided medical and therapeutically benefits to the end user.
Company Size (Fulltime employees)
Year of foundation
2014
Stock Market and Ticker/Symbol/Number
MGWFF
Please specify your partnering goal
END PRODUCT TO CHINA
Funding Status
1ST TRANCHE
Now raising (In USD)
1 MILLION
Headquartner in China
Plan in China
Strategic development into extracting and manufacturing CBG isolate and oil medical, health supplement and cosmetics with our own brand name to China and Asia market
Biotech/Pharma Category
TED FUNG
International Sales Manager 
Functionality