shuyuan PAN China

www.sinopharm.com
our business covers R&D,manufacturing, logistics and distribution of medicinal products.
Partnering Objectives
Headquartner in China
sinopharm
associate director(R&D managing department) 

Mr. Zongde Pan China

Private equity investment institutions in the secondary market, focusing on pharmaceutical consumption and other industries
Website:
NA
Company Size (Fulltime employees)
Year of foundation
2014
Partnering Objectives
Please specify your partnering goal
NA
Headquartner in China
Biotech/Pharma Category
Enbao asset
Investment anlyst 
Functionality

Yan Pan China

Top MNC
Website:
www.Novartis.com
Partnering Objectives
Headquartner in China
Novartis
AD,Business development and Licensing 

Mr. Norberto Pandolfi Orecchia Singapore

Petrone Group Asia Pacific Pte Ltd gives support to Sponsors , CROs , Clinical Research Institutes , Pharma and Biotech company for IMP management and Comparators sourcing.

We are a specialized company in high quality furniture of Investigational Medicinal Product (IMP) and in services for international clinics experimentations , our service has high flexibility in managing clinical trials from phase I to phase IV according to customers’ specific requirements.
Website:
www.petrone.it
Company Size (Fulltime employees)
Year of foundation
1965
Please specify your partnering goal
Comparators sourcing provider
Headquartner in China
Petrone Group Asia Pacific Pte Ltd
Managing Director 
Functionality

Li Pang China

an investment bank in shanghai
Partnering Objectives
Headquartner in China
Tririver Capital
partner 

Dr. Min Pang China

Bayer Healthcare
Bayer Healthcare
Alliance Manager 

Mr. Raffaello Paolini 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
Please specify your partnering goal
Fundraising
Headquartner in China
Biotech/Pharma Category
Assets Information 1
CN109862905A published 2019-06-07 | Methods for treating osteoarthritis by administering linked variants of growth hormone and somatostatin | The present invention relates to the treatment of osteoarthritis. In particular, the present invention relates to peptides for use in the treatment of osteoarthriti
Biotech/Pharma Asset Stage
Medtech Information 1
Diagnostic companion kit OsteoArthritis
Slides Deck
(png, 438.06KB)
Mr. Raffaello Paolini
Regulaxis SAS
R&D Project Manager – East Asian operations development 

Ashutosh Parihar United States

We at Singh Biotechnology (SBT) are interested in meeting with you to exploring possible opportunities for partnering/in-licensing/scientific collaboration.

 

SBT is a start-up biotech company established in 2014. We discover/develop unique and proprietary therapeutic single domain antibodies (sdAbs) for the treatment of a variety of cancers, autoimmune, ophthalmological, and viral diseases by leveraging our propriety novel technology platform. Using this technology platform SBT has been able to generate therapeutic sdAbs that specifically target intracellular molecules of interest that play an important role in the pathogenesis of disease(s). Our lead therapeutic (SBT-100) is a bi-specific sdAbs that specifically targets and inhibits intracellular KRAS and signal transducer and activator of transcription 3 (STAT3) proteins.

Company Size (Fulltime employees)
Year of foundation
2014
Please specify your partnering goal
Raising funds for our lead asset, SBT-100, to complete toxicology studies and then go into phase 1.
Headquartner in China
Biotech/Pharma Category
Assets Information 1
SBT-100 is a monomeric single domain antibody (sdAb) that binds KRAS and STAT3 with nanomolar affinity, inhibits the GTPase activity of KRAS, downregulates P-ERK, inhibits the growth of eleven aggressive human cancer in vitro, and suppresses the growth of human cancers in vivo. SBT-100 is the first sdAb to penetrate the cell membrane and give a therapeutic effect in cancers. It also crosses the blood brain barrier (BBB). Through its anti-STAT3 effects, SBT-100 downregulates the expression of VEGF and PD-L1. The significant suppression of PD-L1 expression caused by SBT-100 emphasizes its immunotherapeutic potential. With our preclinical data, the US FDA has given SBT-100 Orphan Drug Designation for pancreatic cancer and osteosarcoma. In addition, we voluntarily requested a Pre-IND review of our triple negative breast cancer (TNBC) program by the FDA. The Pre-IND briefing packet received a favorable review by the FDA of the TNBC data, our SBT-100 manufacturing process, our proposed IND-enabling toxicology studies in rats and monkeys, and our proposed Phase I studies in patients. All of the patents and technology regarding SBT-100 and our other assets are internal to our company. Nothing has been licensed from an outside entity. The patents for SBT-100 and all our other assets have been approved by the U.S.A., Japan, China, South Korea, Taiwan, Canada, Australia, and every country in Europe. These patents are being processed in every other major country and region in the world.
Biotech/Pharma Asset Stage
Slides Deck
(pdf, 1.52MB)
Singh Biotechnology
Vice President 

Yong H. Park United States

MEDGENE is a T cell therapy biotech start-up (late pre-clinical stage) based in Maryland, USA.
- Focused on developing PD1+ peripheral blood-derived, tumor-reactive CD8+ T cell (PBTL) therapies as a platform for the treatment of solid tumors that are rare, orphan, and have critical (high) unmet need
- PBTL is a simpler, smarter version of TIL
- PBTL is a process to select highly tumor-reactive T cells from a patient's peripheral blood based on the expression of two specific T cell surface markers: PD-1 and/or TIM-3
- After selection, expanded to large quantities, it gets re-infused into the patient via the ACT regimen
- PBTL technology has been patented (issued) already in the US, China, the EU, Japan, Australia
- MEDGENE has robust Clinical Development Pipelines (currently, 9 as monotherapy way)
- Looking for funding for entering Phase I/2 in three pipelines in the US
- Looking for partnering for the Asian market (China, Japan, South Korea)
Website:
www.medgene.us
Company Size (Fulltime employees)
Partnering Objectives
Please specify your partnering goal
Seed (Pre series A) Fundraising of 2M USD/ Partnering in China
Headquartner in China
Biotech/Pharma Category
Biotech/Pharma Asset Stage
MedGene Therapeutics
CEO 
Functionality

Miss Heidi Pavliska Netherlands

Business and scientific consultant driving business and corporate match making in drug discovery and development across Europe and in the US
Company Size (Fulltime employees)
Year of foundation
1999
Partnering Objectives
Please specify your partnering goal
Generation n t innovative interactions and relationships across Europe and with Asia.
Headquartner in China
Pavliska Industries
Senior Director Business Development 
Functionality