Biolingus Switzerland

At Biolingus, we believe we can make life better for many people in the world, not just in rich countries, but across the globe.
BioLingus is an award-winning Swiss biotech company spearheading the development of oral (sublingual) and mucosal delivery of peptides and proteins. Our technology is "inspired by nature" using applied bio-engineering, resulting in novel bio-mimetic materials for drug delivery. Our company focusses on the development of its own products on the treatment of chronic diseases, such as diabetes, obesity and inflammatory diseases.
BioLingus’ main office is in Switzerland, with satellite companies in Hong Kong and Australia.
See also video made by the Swiss Chinese Chamber of Commerce : https://www.linkedin.com/posts/yvesdecadt_icbc-vischer-gunvor-activity-6737745258496434176-8BZc
Website:
www.biolingus.ch
Company Size (Fulltime employees)
Year of foundation
2014
Please specify your partnering goal
(1) Outlicensing our lead assets for China - Liraglutide oral (sublingual) - Exenatide oral (sublingual) - insulin + (fixed dose combination of insulin with exenatide ; sublingual) (2) partnering on development of proprietary peptides
Now raising (In USD)
30 MM
Headquartner in China
Plan in China
Commercializing all our products
Biotech/Pharma Category
Assets Information 1: Name|Description|Indications|Stage|IP countries
Liraglutide SL|sublingual liraglutide|obesitas, diabetes type II|phase 1b/2a|
Assets Information 2
Exenatide SL|sublingual exenatide|obesitas, diabetes type II|preclinical|
Biotech/Pharma Asset Stage
Yves Decadt
CEO 
Functionality

Cerevel Therapeutics United States

Cerevel Therapeutics is a clinical-stage biopharmaceutical company that combines a deep understanding of the biology and neurocircuitry of the brain with advanced chemistry and central nervous system (CNS) receptor pharmacology to discover and develop new therapies.

We seek to transform the lives of people suffering from neuroscience diseases, including Parkinson’s disease, epilepsy and schizophrenia, through the development of novel therapies. We have built a highly experienced team of senior leaders and neuroscience drug developers who combine a nimble, results-driven biotech mindset with the proven expertise of pharmaceutical company drug discovery and development.
Company Size (Fulltime employees)
Year of foundation
2018
Stock Market and Ticker/Symbol/Number
NASDAQ: CERE
Please specify your partnering goal
Interested in better understanding the current CNS biopharma landscape in China
Headquartner in China
Medtech Development Stage
Scott Lewis
Corporate Development & Strategy 
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

Global Clinical Trials (GCT) United States

Global Clinical Trials (GCT) is a premium contract-research organization (CRO) that offers support for the clinical Phase I-IV studies as well as post-marketing activities to Big Pharma, small and medium-sized biotech enterprises, groups and funds, as well as large universities and institutions. Headquartered in Princeton, USA, GCT offers both local and global support through 10 own operational offices in Bulgaria, Czech Republic, Georgia, Hungary, India, Kazakhstan, Latvia, Lithuania, Estonia, Moldova, Poland, Romania, Russia, Slovakia, Ukraine.
GCT team, that now consists of over 100 full-time clinical research professionals, gives individualized attention to each project and provides full range of services following the latest GCP, EMA and FDA guidelines at every stage of product development path. Our monitors and project managers are all certified clinicians experienced in GCP clinical research. Our experience, competent staff, close contact with the KOLs and the immense enrollment potential of the covered region ensure fast study start-up and compliance with the set timelines.
GCT owns 400 sq.m. (4300 ft2) Drug Storage and Distribution facility in St. Petersburg, Russia. It is fully equipped, disaster protected and has multiple modes of storage (ambient, climate controlled, refrigerated, frozen). High standards of work and client satisfaction are proved by the fact that more than 80% of the business come from repeat clients.
Since 2006 GCT is also an Exclusive Partner of “The White Nights” International ophthalmology congress in Russia.
Company Size (Fulltime employees)
Year of foundation
2001
Stock Market and Ticker/Symbol/Number
N/A
Please specify your partnering goal
Networking, new business opportunities
Headquartner in China
Plan in China
GCT is looking for potential new business opportunities, offering full-service clinical trials support worldwide for Chinese pharma companies.
Biotech/Pharma Category
Biotech/Pharma Asset Stage
Medtech Development Stage
Your Service Name
clinical trials, market authorization, registration, consulting
Service Description
logistics, regulatory services, project and site management, pharmacovigilance, medical monitoring, data management, biostatistics, medical writing, GDPR and DPO, EU Legal representation,
Target Client Type
Pharma, Biotech, Device companies
Aleksandr Stiblo
LinkedIn logo Director, Business Development 
Functionality

Jupiter Orphan Therapeutics Inc. (JOT) 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
Christer Rosen
Chairman & CEO 
Functionality

Regulaxis SAS France

Regulaxis SAS is a French biotech company created in 2013 to develop innovative therapies for human clinic based on new synthetic peptides regulating cell growth and differentiation.

Regulaxis is specialized in the regulation of cell proliferation and/or cell differentiation. The potential therapeutic applications covered by our patents are very broad, especially in the areas of joint/bone or nerve cell regeneration, but also in cancer and related metabolic diseases (diabetes, obesity …).
Our mission is to grant licenses of innovative molecules in a pharmaceutical company after completion of phase II clinical proof of concept.

Regulaxis is strategically focused only on high unmet medical needs but has elected as its first priority:
regeneration of articular cartilage using intra-articular injections of its lead candidate REG-O3.

Company Size (Fulltime employees)
Year of foundation
2013
Looking for
Please specify your partnering goal
Investor or licensee
Funding Status
1.1 mEUR (10 mRMB)
Now raising (In USD)
25 mUSD
Headquartner in China
Plan in China
Incorporate WFOE as a start to incubate Chinese patent CN109862905A published last 2019 06 07and proceed with Mainland fundraise to sponsor- Finished Pharmaceutical manufacturing operations in China- Engage discussions with Central NMPA to approve our Chinese Clinical Trial designBringing earlier access for Chinese patients to such first therapeutic treatment of OsteoArthritis of the knee,through out licensing to a major Chinese pharmaceutical company
Biotech/Pharma Category
Assets Information 1: Name|Description|Indications|Stage|IP countries
IP registered Mainland China in 2019
Biotech/Pharma Asset Stage
Medtech Category
Medtech Information 1, Device Name|Description|Development Stage|Licensed Countries
First in Class new MoA peptide based DMOAD
Medtech Information 2
NeuroEndocrine Tumors
Target Client Type
Chinese pharma with established market position in OsteoArthritis
Slides Deck
(png, 430.99KB)
Dr Matthieu CHAREYRE
Dr Matthieu CHAREYRE
LinkedIn logo Chief Business Development Officer - Global Pharmaceutical Operations 
Functionality

Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd China

Kelun-Biotech Biopharmaceutical is a subsidiary of Kelun Pharmaceutical Group established in 2016

Looking for antibody and samall molecular out-license and in-license

Headquartner in China
Biotech/Pharma Asset Stage
Chunlin Li
BD btlichl@kelun.com 

Trove Therapeutics, Inc. United States

Trove is a semi-virtual biotech start-up located in Rockville, Maryland, USA, developing an advanced biologic asset and seeking funding and partners to conduct clinical trials in respiratory disease. We have data and drug supply on our lead, clinical-stage biologic asset to support up to 3 clinical trials in different respiratory conditions (2 x Phase 1b/2a in COVID and lung transplant; and 1 x Phase 2 in chronic sinusitis). Our biologic, called Therabron, is a replacement for a normally abundant native protein that is deficient in our targeted indications. Replacement therapies have a high approval rate with FDA (>70%) and patients with genetic deficiencies can be selected in some trials to increase our chances of demonstrating efficacy. Therabron was safe in 3 early studies. At present, the quickest path to an approval is likely an Emergency Use Authorization in severe COVID-19 patients, so we're looking for an initial $2M seed/Series A round to fund a Phase 1b/2a clinical trial then need another $16M to produce more drug and perform a convincing Phase 2 trial. We are already talking to several potential corporate partners, have signed one CDA with a top 5 pharma, and a relatively small amount of investment in clinical proof of concept demonstrations will attract at least one partner. Once clinical POC is established in targeted indications, we plan to exit via sale/acquisition or out-license. Our markets are large (3 products x >$1B each US) and deal comps in the respiratory space are $250M each and up. We can maximize our ROI by out-licensing the first indication and re-investing upfront license payment proceeds to advance the drug in further indications, depending on what happens in each field/indication and what we (management team and investors) decide to do.
Company Size (Fulltime employees)
Year of foundation
2018
Stock Market and Ticker/Symbol/Number
private
Please specify your partnering goal
We seek a partner that will license or acquire our lead product, a clinical stage biologic, after a Phase 2 trial. We have a data package and sufficient drug to perform up to 3 clinical trials as described above. Ideally, the partner will have expertise in developing drugs for respiratory diseases.
Funding Status
Pre-seed
Now raising (In USD)
$2M seed round to fund a Ph1b/2a trial, then a $16M Series A round after Ph1b/2a trial completed to fund a Phase 2 trial.
Headquartner in China
Plan in China
To find a licensing partner that has the resources and expertise in respiratory drug development and biologics to advance our clinical-stage candidate, called Therabron, through clinical trials in one or more respiratory indications in China. We prefer to co-develop Therabron in the US and have a good working relationship with our Chinese partner to avoid unnecessary duplication of work.
Assets Information 1: Name|Description|Indications|Stage|IP countries
Therabron (rhCC10 protein)|recombinant human protein - biologic|multiple respiratory|Ph1 & Ph2|none
Biotech/Pharma Asset Stage
Aprile Pilon
CEO 
Functionality