Dan Ring United States

We are a late-stage biopharmaceutical company committed to developing and commercializing products to treat rare diseases where there is an unmet medical need.
Stock Market and Ticker/Symbol/Number
SNGX
Please specify your partnering goal
Out licensing CTCL program
Headquartner in China
Biotech/Pharma Category
Assets Information 1: Name|Description|Indications|Stage|IP countries
Hypericin||CTCL|Ph 3 completed|
Biotech/Pharma Asset Stage
Soligenix, Inc.
Vice President, Business Development & Strategic Planning 
Functionality

Christer Rosen United States

JOT is a virtual company with its base operation in Jupiter, FL. JOT is in position to quickly come to market with a platform product effective to treat 12 or more indications including Alzheimer’s Disease. The proprietary patented product, JOTROL, is very safe, oral, naturally based and multi-functional. JOTROL will be very effective with high social and economic impact within a reasonable timeframe. Relationships have been developed with scientists at various institutions, such as University of Miami (“UM”), MIT, Harvard, Georgetown University and Murdoch Childrens Research Institute, AU. This setup has made it possible to gain access to laboratory work, scientific information, pre-clinical development and scientific expertise in an extremely cost effective and efficient way. JOT will conclude clinical trials by utilizing a contract manufacturer and Clinical Research Organizations, involvement by its scientific advisors as well as support from patient organizations thereby keeping its fixed overhead extremely low for a Biotech company. A Phase I trial is presently ongoing with results expected in Q1,2021. Two Phase II rare disease trials, are expected to be started in H2 of 2021 with possible accelerated approvals from FDA. Partial financing for those are expected to be received from NIH. A Phase II trial in Alzheimer’s is also planned to be executed in parallel. Financing for the Phase I study has been granted by NIA (National Institute of Aging). Financing for a larger Phase II study is also expected to be financed by a NIA consortium (up to $75 million). JOT is prepared to add a commercial organization to market its product in North America while out-licensing marketing and sales operations for the rest of the world.
Company Size (Fulltime employees)
Year of foundation
2016
Please specify your partnering goal
Out-license our platform product to a reputable Chinese partner.
Funding Status
Series A
Now raising (In USD)
$15 Million
Headquartner in China
Plan in China
Out-license our JOTROL platform product applicable to 12 or more indications.
Assets Information 1: Name|Description|Indications|Stage|IP countries
JOTROL|Patented First and Only resveratrol product that can be disease modifying without side effects.|MPS-1, MELAS, Friedreich's ataxia and other ataxias, Mild Cognitive Impairment, Alzheimer's Disease|Phase I completed mid-March|N/A
Biotech/Pharma Asset Stage
Jupiter Orphan Therapeutics Inc. (JOT)
Chairman & CEO 
Functionality

ENRIQUE SANCHEZ Canada

Canadian IVD company with core competencies in the fields of Thrombosis, Haemostasis and oncology, with innovative technologies, we collaborate internationally with technology development companies and health-care stakeholders to develop and manufacture customized reagents and diagnostic solutions.
Company Size (Fulltime employees)
Year of foundation
1999
Please specify your partnering goal
Find a Partner in oncology and / or Thrombosis & Haemostasis
Headquartner in China
Plan in China
Find a Partner in China interested in marketing special Thrombosis & Haemostasis tests, and Femtelle in oncology.
Biotech/Pharma Asset Stage
Medtech Category
Medtech Information 1, Device Name|Description|Development Stage|Licensed Countries
FEMTELLE|FEMTELLE® is intended for the quantitative measurement of human Urokinase-type Plasminogen Activator (uPA) and human Plasminogen Activator Inhibitor Type-1 (PAI-1) in detergent extracts of breast tumor tissue. uPA and PAI-1 are clinically validated independent prognostic markers in breast cancer and have reached the highest Level of Evidence (LoE-1) according to the “Tumor Marker Utility System”.|MARKETED|NONE
Medtech Development Stage
BIOMEDICA DIAGNOSTICS
Mr. 
Functionality

Wu Sarah United Kingdom

中英生命科学医疗项目合作
Website:
在建
Headquartner in China
China Medlink
CEO 
Functionality

Heather Schwoebel United States

Alloy is making a humanized transgenic antibody discovery platform, developed within a large pharmaceutical company, broadly available. Our business model includes unlimited access under royalty free terms. Alloy’s strategic plan is to include additional platforms in the protein engineering space that can be synergistically incorporated into our platform, thereby increasing the value offered to licensees.
Website:
www.alloytx.com
Headquartner in China
Plan in China
partnering and out-licensing
Alloy Therapeutics
Senior Director of BD 
Functionality

Dong Sheng China

As an investment and management platform established by UK-listed company Cathay International Holdings Limited, Lansen has built up pharmaceutical segment, health segemtn and cosmetic segment. Lansen has been listed in Stock Exchange of Hong Kong Limited (SEHK) on May 7, 2010. Lansen's top products are in rheumatology and dermatology area, and Lansen has established an extensive distribution network, with more than 300 frontline sales staff and more than 1500 distributors. By licensing in promising products at commercial stage and clinical stage, or other cooperation patterns, Lansen plans to expand to more diseases medication market, including rheumaotlogy, dermatology, orthopedics and nephrology.
Company Size (Fulltime employees)
Year of foundation
2002
Stock Market and Ticker/Symbol/Number
0503 (HKG)
Looking for
Headquartner in China
Lansen Pharmaceutical Holdings Limited
BD Manager 
Functionality

h michael shepard 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
Enosi Life Sciences
CSO and CEO 
Functionality

Dave Sheppard United States

MedWorld Advisors is an international M&A Services Firm. We represent medical technology companies from the US, EU and Israel that want to enter the China market. We facilitate licensing, commercialization and acquisition deals between our clients and larger companies / investors in China. We are based in Boston in the U.S. We also have an operation in Hong Kong to help facilitate deals, as helpful.
Company Size (Fulltime employees)
Year of foundation
2015
Please specify your partnering goal
We currently have 10 Medical Technology projects that may be interesting for the China market. We seek to meet appropriate China partners for these projects.
Headquartner in China
Plan in China
We have projects in medical imaging, image processing, endoscopy, endo-vascular, hemodynamics, oximetry, digital health, wearables, and wound care that may be interesting for the China market.
Medtech Information 1, Device Name|Description|Development Stage|Licensed Countries
Multiple Projects|Open for Licensing / Acquisition|FDA Cleared|US, EU and Israel
Medtech Development Stage
MedWorld Advisors
Managing Director 
Functionality

George Simeon United States

Curevo is a clinical stage company dedicated to bringing next generation vaccines that offer effectiveness, safety, tolerability, and production advantages to the market, quickly and efficiently.
Curevo will combine excellence in protein science and adjuvant technology to speed safe and highly effective vaccines from the bench through clinical development.
Curevo will focus on vaccine-preventable illnesses that are common in both the Asian and US markets and for which current vaccine products are not available.
Curevo’s goal is to rapidly advance innovative new vaccine candidates from research laboratory to clinic by joining forces with South Korean Mogam Institute for Biomedical Research and GC Pharma.
Curevo's lead product, a Zoster (Shingles) Vaccine, has completed Phase I and shown promising results. We are targeting a unique position in the $20B (by 2030) Varicella Zoster Virus vaccine market.
Company Size (Fulltime employees)
Year of foundation
2018
Looking for
Funding Status
Raising Series-A
Headquartner in China
Plan in China
As a premium and high margin segment, the shingles vaccine market represents a significant opportunity for local, regional, or global players.
Curevo Vaccine
CEO 
Functionality

Dr Di Simon China

Wanbang Biopharmaceuticals (Wanbang Biopharma) is a core member of Shanghai Fosun PHARMACEUNCAL (group) Co., Ltd.(Fosun Pharma”, Stock code: 600196-SH,02196-HK).
Wanbang Biopharmaceuticals (Group) Co., Ltd
高级BD经理