China Medlink United Kingdom

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

Connexin Therapeutics Ltd. United Kingdom

Connexin Therapeutics Ltd. is a UK-based biopharmaceutical company specializing in the discovery and development of drugs targeting connexins, initially for the prevention of vision loss and blindness associated with the eye disease known as glaucoma. While there are a variety of glaucoma subtypes, a common hallmark is the progressive loss of vision due to the gradual cell death in the retina and optic nerve triggered by elevated intraocular pressure. Many drugs are available to reduce intraocular pressure, yet none have been shown to directly protect cells in the retina or optic nerve, and hence prevent them from dying. Thus, vision loss inevitably occurs, even in well-treated patients, and severe vision impairment remains common in these patients.
For 20+ years, our scientific co-founder, Dr. Stewart Bloomfield, has researched and published extensively on the connexin-mediated mechanisms by which elevated intraocular pressure causes cell death in the retina and optic nerve, resulting in vision loss. His research has demonstrated three key points:

1. Retinal and optic nerve cell death is mediated by the bystander effect, which, in turn, mediated by a protein called connexin 36; and

2. Inhibition of connexin 36 prevents further loss of vision in glaucoma; and

3. This inhibition can be achieved using a small molecule drug.

Thus, our goal at Connexin Therapeutics is to develop and partner novel compounds which block connexin 36, thereby preserving vision and potentially preventing blindness in patients with glaucoma. Importantly, glaucoma patients with either elevated or normal intraocular pressure will benefit from retinal neuro-protectants, even in the presence of aggressive attempts to reduce intraocular pressure via drugs or surgery. Other ophthalmic diseases which may benefit from connexin inhibition include subtypes of glaucoma (i.e., normotensive glaucoma), retinitis pigmentosa, and the prevention of corneal scarring secondary to eye surgery. These are indications which may be pursued as the company grows.
In addition to our work with connexin 36 in glaucoma, we may have an opportunity to discover and develop a novel connexin 45 inhibitor. Preliminary work from our laboratory suggests that inhibiting connexin 45 has protective benefits in a range of ischemic ophthalmic conditions, such as diabetic retinopathy. Thus, we have the opportunity to advance two programs from the current round of financing into full development or even licensing.
Interest from multinational pharmaceutical companies in novel compounds to treat ophthalmic conditions is extraordinarily high, as these companies recognize that the rapidly aging population, coupled with significant unmet needs and favorable reimbursement policies, all make for attractive licensing opportunities for companies like Connexin Therapeutics. Thus, we anticipate initiating licensing discussions with pharmaceutical companies as novel connexin inhibitors emerge from our efforts.
Connexin Therapeutics raised ~£150,000 in Seed financing in early 2019. These funds are being used to synthesize and test novel small molecules in animal models of glaucoma. These compounds are based on a molecule which has already demonstrated efficacy in mouse models of glaucoma. Thus, these data supplement and extend the work already published.
We are currently raising ~£2,000,000 to optimize our lead compounds. After ~8-10 quarters of work we anticipate having a library of patentable compounds which are highly selective for connexin 36, backed by primate data. We will have a second compound which inhibits connexin 45 for diabetic retinopathy. Future financing rounds will take one or both leads into clinical trials, while also fueling our expansion into other indications with this same mechanism of action.
Company Size (Fulltime employees)
Year of foundation
2018
Looking for
Please specify your partnering goal
Raise capital
Funding Status
Seed B round
Now raising (In USD)
2700000
Headquartner in China
Plan in China
Vision loss due to glaucoma and other ophthalmic conditions is a large and growing problem. Our intention is to seek licensing partners in China and across Asia once our compounds are more mature.
Biotech/Pharma Category
Assets Information 1: Name|Description|Indications|Stage|IP countries
CxTX-001|Small molecule connexin 36 inhibitor|Vision protection in glaucoma|Lead optimization|None
Biotech/Pharma Asset Stage
Carlos Velez
Carlos Velez
CEO 
Functionality
Dr Kshitij Soni
LinkedIn logo CEO 
Functionality

CStone China

CStone Pharmaceuticals is a biopharmaceutical company focused on developing and commercializing innovative immuno-oncology and precision medicines to address the unmet medical needs of cancer patients in China and worldwide. Established in 2015, CStone has assembled a world-class management team with extensive experience in innovative drug development, clinical research, and commercialization. The company has built an oncology-focused pipeline of 15 drug candidates with a strategic emphasis on immuno-oncology combination therapies. Currently, 5 late-stage candidates are at pivotal trials. With an experienced team, a rich pipeline, a robust clinical development-driven business model and substantial funding, CStone's vision is to become globally recognized as a leading Chinese biopharmaceutical company by bringing innovative oncology therapies to cancer patients worldwide.
Ping Zhao
Greater China General Manager and Head of Commercial Operations 
Functionality

Curevo Vaccine 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.
George Simeon
CEO 
Functionality

D2M Biotherapeutics United States

A human-genetics driven next generation immunity-oncology company
Website:
www.d2mbio.com
Looking for
Headquartner in China
Nan Bing
CEO 
Functionality

Dawn Biopharmaceuticals Inc. United States

Dawn Biopharmaceuticals Inc (DBI) is a US firm founded by Gordon Lee, MD (UK MBChB), MBA (Wharton) who has access to a proprietary cell-based immunotherapeutic product for clinical development in the US. The product is a multivalent cancer therapy that integrates multiple anti-cancer mechanisms in one modifiable platform. The product is tumor-homing, disables the local tumor defenses and expresses a therapeutic cytokine in the cancer - but not systemically.

(Please note that the website is pending.)

Website:
dawnbio.net
Company Size (Fulltime employees)
Year of foundation
2020
Please specify your partnering goal
Strategic pharmaceutical or capital partner to accompany into Pre-IND and clinical trials.
Funding Status
Initial round
Headquartner in China
Plan in China
Open to partnerships with Chinese firms that have a proprietary small molecule or biodrug that could be encoded into our platform with the benefits of wider scope of applications, tumor-centric molecular therapeutic delivery, avoidance of peripheral (extra tumoral) actions and effects, and vectoring of high payload(s) for multi-arming.
Biotech/Pharma Asset Stage
Gordon Lee
Founder 
Functionality

DIMITAR DIMITROV Bulgaria

Micar Innovation is a drug discovery factory. The company has found a niche where it is able to create a large societal impact by improving the quality of life through discovery novel blockbuster drug molecules for a large class of diseases (Pipeline). Micar Innovation focuses on entire drug discovery process using improved structure based insilico drug design from scratch till Preclinical phase with advanced predictions of activity, selectivity and ADMET

Company Size (Fulltime employees)
Year of foundation
2016
Please specify your partnering goal
Drug Discovery
Funding Status
raising
Now raising (In USD)
2500000
Headquartner in China
Biotech/Pharma Asset Stage
Investment Focus
Oncology project
Slides Deck
(pdf, 939.67KB)
CEO 
Functionality

DivaOra Group Russia

Manufacturing, whole sale innovation product EYEIMPROVER.com - the stimulator for the eyes
Company Size (Fulltime employees)
Year of foundation
2016
Funding Status
investment, strategy investor
Headquartner in China
Plan in China
We want move our business from CHINA. We searshin investment and we are ready for relocation.
Olga Oshurkova
CEO & Owner 
Functionality

Drive Therapeutics, LLC United States

Drive Therapeutics is developing a novel, long acting, bispecific nucleic acid therapeutic to block the angiogenesis, inflammation, and fibrosis underlying retinal disease. Drive’s lead program is a bispecific aptamer therapeutic made up of two well validated components: a pan-specific anti-VEGF-A aptamer and an anti-Interleukin-8 (IL8) aptamer. Drive’s lead program will mitigate poor patient response to existing anti-VEGF therapy, improve outcomes and reduce patient burden. By targeting both angiogenesis and a critical immune pathway that drives both inflammation and angiogenesis, Drive’s bispecific inhibitor is the key to overcoming the limitations of VEGF monotherapy. In addition to current candidates, Drive’s aptamer therapeutic discovery platform will allow for streamlined, efficient development of new therapies to pathologically relevant ophthalmologic targets.
Company Size (Fulltime employees)
Year of foundation
2019
Please specify your partnering goal
Looking for a partner to move the program forward to get proof of concept
Funding Status
Seed Stage
Now raising (In USD)
600k- 2.0 MM
Headquartner in China
Plan in China
We feel that our product would be very successful in the China market. A co-development deal would be ideal.
Biotech/Pharma Category
Ryan Quick
Co-founder and COO 
Functionality