GenScript USA United States

Synthetic biology company, DNA cold data storage
Website:
GenScript.com
Company Size (Fulltime employees)
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Investment for DNA cold data storage
Headquartner in China
Dr. Michael Lau
Director 
Functionality

GIG China

GIG, one of the leading healthcare investment institute, was founded in Shenzhen in 2001. AUM is RMB ¥20b. It has invested in 80+ healthcare companies. 22 went IPO. GIG has 90+ staff in team with operating offices in Shenzhen, Shanghai, Beijing, Nanjing and Hongkong.

Website:
www.szgig.com
Company Size (Fulltime employees)
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potential investing targets and collaborations
Headquartner in China
Medtech Development Stage
Denise Chen
Partner 
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
Headquartner in China
TED FUNG
International Sales Manager 
Functionality

Grektek United States

The everbeat platform is being offered by Grektek, whose mission is to help dramatically improve cardiac care. We created everbeat to improve our ability to take care of ourselves, especially as we get older, and with a strong focus on heart health. Most existing solutions related to cardiac care are unattractive and cumbersome, and brand the patient as weak or sickly. At Grektek, we designed everbeat to be elegant and simple, allowing patients to take better care of themselves with dignity and comfort. We also believe that patients will enjoy the everbeat solution, which means they will use it consistently for a long time – and sustained use of a cardiac monitoring platform is essential to getting healthy.

Website:
everbeat.org
Company Size (Fulltime employees)
Year of foundation
2016
Please specify your partnering goal
Medical organizations looking to deploy remote patient monitoring solutions that can be proved to help their patients.
Headquartner in China
Biotech/Pharma Category
Assets Information 1
Everbeat Watch|Watch that can take a clinical grade ECG||USA
Biotech/Pharma Asset Stage
Medtech Category
Medtech Information 1
Everbeat | wearable ECG band | USA
Medtech Development Stage
Mr. Greg Eoyang
CTO 
Functionality

Hanhai Biolabs, Inc. United States

Cross border life science accelerator and angel investor based in San Francisco Bay Area and Wuxi, China.
Company Size (Fulltime employees)
Please specify your partnering goal
Greater China rights
Headquartner in China
Dr. Alex Zhang
CEO 
Functionality

hearing sanjiu pharmacy China

tcm,
Website:
www.crssj.com
Partnering Objectives
Headquartner in China
weiping he
assistant professor 

Immetas Therapeutics United States

Immetas discovers and develops novel therapeutics that modulate the innate immune system to treat age-related cancers and inflammatory diseases. The company’s approach is based on emerging evidence that chronic low-grade inflammation is a fundamental process governing aging and age-related diseases, and anchored in clinical evidence to mitigate development risk. Immetas was founded by J. Gene Wang, MD, PhD, a veteran in discovery and translational drug development in immunology/ inflammation and oncology, and David Sinclair, PhD, Professor of Genetics at Harvard Medical School and a leader in the molecular mechanisms of aging. The lead program in the company’s growing pipeline is focused on engineering bispecific antibodies to modulate inflammation in the tumor microenvironment and overcome resistance to the conventional immune checkpoint therapies. Learn more at www.immetas.com
Partnering Objectives
Headquartner in China
J. Gene WANG
CEO 

ImmunoBiochem Canada

ImmunoBiochem is an immuno-oncology biopharmaceutical company that has developed a disruptive approach to targeting unique proteins amplified in cancer secretomes. These targets are secreted from cancer cells and accumulate in tumors, but not in normal tissues, and are constantly recycled in the tumor microenvironment. This novel approach enables the selective and efficacious delivery of immunomodulatory and chemotherapeutic payloads into relevant subsets of cells within the tumor microenvironment, including tumor cells, immune cells and tumor-supporting stroma.
ImmunoBiochem’s IMB-213I candidate delivers a potent innate immune system agonist for the treatment of highly heterogeneous solid tumors, such as TNBC, pancreatic and ovarian cancers.
ImmunoBiochem's IMB-212 candidate delivers a potent cytotoxic payload into difficult-to-treat solid tumors, particularly where no suitable surface targets and no biologics are available.
Company Size (Fulltime employees)
Please specify your partnering goal
Opportunities for collaborations and joint development
Headquartner in China
Assets Information 1
IMB-213I|Novel Immunomodulatory Antibody Conjugate|Solid Tumors|
Assets Information 2
IMB-212|ADC against a novel cancer secretome-based target|Solid Tumors|
Biotech/Pharma Asset Stage
Dr. Anton Neschadim
CEO 
Functionality

Incuron, Inc. United States

Incuron is a private clinical-stage company that develops a novel class of synthetic small molecules, Curaxins, with a unique multi-targeted mechanism of antitumor activity. These chromatin damaging agents interfere with histone/DNA binding causing decondensation of chromatin in tumor cells, functional inactivation of histone chaperone FACT, and simultaneous effect on a set of universal previously undruggable targets, leading to inhibition of pro-cancer transcriptional factors, MYC, NF-kB, HIF1a, and HSF-1, and activation of the tumor suppressor p53, as well as induction of type I interferon response.
Key advantages of curaxins based on current preclinical and early clinical data include:
- novel mechanism of action that would bring the additional treatment option for advanced and relapsed tumors, as well as potential to overcome resistance to previous treatments;
- favorable pharmacology and manageable safety profiles;
- low potential for serious drug-drug interactions providing opportunities for combinatorial therapeutic regimens;
- broad activity in different tumor types that may open wider market opportunities;
- focused phase 2 clinical study program can establish faster clinical proof of concept and build toward accelerated regulatory approval.
Incuron owns a worldwide patent portfolio, including the composition of matter and therapeutic uses of the compounds.

Website:
incuron.com
Headquartner in China
Assets Information 1
The clinical lead curaxin CBL0137 demonstrated dose-dependent, nonclinical efficacy in several preclinical adult and pediatric solid and hematological tumor models, and synergistic activity with multiple conventional drugs. Two Phase 1 clinical trials of CBL0137 in advanced solid tumors (oral and IV formulations) were completed with the results presented at the 2020 ASCO Virtual Annual Meeting (Poster 313 (abstract 3583) and Poster 337 (abstract 3607)). CBL0137 demonstrated favorable pharmacology, a manageable safety profile, and preliminary evidence of antitumor activity with protracted stable disease. It was also studied in patients with hematologic malignancies. Additionally, a Phase I clinical trial of intra-arterial administration to patients with sarcoma or melanoma of extremities is ongoing (NCT03727789). A clinical program in pediatric oncology iscurrently under development. CBL0137 crosses the blood-brain barrier, supporting potential utility in CNS tumors.
Biotech/Pharma Asset Stage
Kristina Zakurdaeva
CEO 
Functionality

Innova Therapeutics United States

Innova Therapeutics is a Charleston, South Carolina based biotechnology company developing a monoclonal antibody (mAb) platform targeting a protein that is highly expressed in various solid cancers and shown to correlate with patient outcome. The lead humanized mAb has been selected and is designated as IVT-8086. Innova’s platform technology is initially focused on targeting cancers including pediatric osteosarcoma, sarcomas, breast cancer and pancreatic cancer. The opportunity for this anticancer therapy as a monotherapy and in combination with other chemotherapy agents will expand across other solid tumors. The focus on pediatric osteosarcoma as one of the initial targets will allow a fast-regulatory approval, with the opportunity to obtain a Rare Pediatric Disease priority review voucher. Because Priority Review Vouchers (PRVs) may be sold, a secondary market for the vouchers has emerged, with revenue ranging between $80M and $350M.

The Innova team includes industry leaders with broad pharmaceutical development experience including extensive successful cancer therapy development, as well as life science leadership, manufacturing, preclinical research and safety, business development and regulatory. The team is led by one of the co-founders and CEO, Robert Ryan, Ph.D., who is a successful serial biotech entrepreneur.

The Innova management team was previously the management team in the biotech, Scioderm. Scioderm was the first biotech to receive “Breakthrough Therapy” designation from the FDA for their therapy for an orphan disease. In addition, Dr. Ryan led the successful sale of Scioderm to Amicus in 2015 for approximately $957M (4th largest venture capital (VC) backed exit of 2015 in the biotech/pharmaceutical space), in a period of less than 2.5 years from initiation of the company with a total spend of less than $22M.

Company Size (Fulltime employees)
Partnering Objectives
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A total of $7M in non-dilutive funds has been obtained to date to fund the identification and manufacture of the lead humanized monoclonal antibody (IVT-8086). We are currently raising a Series A financing of US$25-30M to fund our lead candidate, IVT-8086 through the following activities over the next 30 months: • Scale up and production of IVT-8086, • Pre-IND meeting with the FDA, • complete Investigational New Drug (IND) enabling toxicology studies, • file the IND, • initiate and complete Phase I/2 monotherapy studies in pediatric osteosarcoma (registration), sarcomas, triple negative breast cancer, and pancreatic cancer, • and initiate and complete a Phase I combination therapy study.
Headquartner in China
Biotech/Pharma Category
Assets Information 1
IVT-8086|humanize monoclonal antibody|Cancer, including initially osteosarcoma, pancreatic and breast|global
Assets Information 2
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Assets Information 3
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Biotech/Pharma Asset Stage
Slides Deck
(pdf, 1.19MB)
Dr. Robert Ryan
Dr. Robert Ryan
LinkedIn logo Chief Executive Officer 
Functionality