AnHeart Therapeutics China

AnHeart Therapeutics is an oncology-focused clinical stage biopharmaceutical company headquartered in Hangzhou, China with offices in Beijing, Shanghai and New York. The company’s pipeline consists of three clinical stage assets: Taletrectinib, a next-gen ROS1 and NTRK inhibitor currently in Phase 2; an mIDH1 inhibitor ready for Phase 2 for low grade glioma, cholangiocarcinoma, AML and other tumors; and an AXL inhibitor in Phase 1 for overcoming resistance in various tumors.
Company Size (Fulltime employees)
Year of foundation
2018
Please specify your partnering goal
1/Funding Raising for Series B; 2/Pipeline Asset EU and Korea out licensing; 3/In licensing new clinical PoC oncology assets
Headquartner in China
Assets Information 1
Taletrectinib|next-gen ROS1/NTRK inhibitor, the leading program, currently in a Phase 2 trial in China and ex-China global trials to start in early 2021|ROS1+ NSCLC|Global
Assets Information 2
AB-218/DS-1001|a potentially best-in-class mIDH-1 inhibitor in co-development with Daiichi Sankyo (Japan rights), to start with ex-Japan global Phase 2 trials in glioma and conduct preclinical and clinical POC studies in other indications|IDH1+ Lower Grade Glioma|ex-Japan
Assets Information 3
AB-329/DS-1205|a potentially best-in-class AXL inhibitor, to start with preclinical and clinical POC studies in multiple indications|combo with PD-1 ab for NSCLC|Global
Biotech/Pharma Asset Stage
Dr Lihua  Zheng
Dr Lihua Zheng
LinkedIn logo CBO & co-Founder 
Functionality
Dr. Weiqing Wang
Associate Director of BD 
Functionality
Dr. Akira Liu
Director of BD 
Functionality

Biosion Inc., China

iosion is a global biotechnology company focusing on the discovery and clinical development of innovative biologicals for unmet medical needs. Leveraging our proprietary H³ (High-throughput High-content High-efficiency) antibody platform and SynAb™ technology, Biosion is able to undertake a deep discovery of antibody drug candidates with superior properties, multiple differential choices, and diversified clinical applications. Based on its integrated antibody discovery engine and fueled by our corporate motto of "Innovation for Cures", Biosion is committed to bring next generation innovative drugs to patients around the world.

During the past several years, Biosion team has successfully built up multiple therapeutic antibody discovery pipelines for in-house development and for collaboration with our partners, thus enabling us to accelerate and broaden our innovative drug development capabilities for delivering novel drugs to patients in needs.
Company Size (Fulltime employees)
Year of foundation
2013
Please specify your partnering goal
Seeking partners in big pharma or established biotech companies to co-develop or license assets from Biosion's pipeline or to explore new collaborations for innovative antibody discovery by using our proprietary H³ antibody discovery platform and SynAb™ technology. We are also seeking additional investment to support advancement of our innovative antibody pipeline move into the clinic.
Headquartner in China
Assets Information 1
BSI-045B|TSLP: High affinity superior humanized antibody for the treatment of asthma and atopic dermatitis (Ex-China global rights)|Severe Asthma|Pending
Assets Information 2
BSI-03802|CD40: Humanized antibody molecule with superior agonist activity (Ex-China global rights)|solid cancer|Pending
Assets Information 3
BSI-001|HER2: hu5G9, best-in-class efficacy partner of trastuzumab and for next generation HER2 ADC development|HER2+ cancer|PCT
Biotech/Pharma Asset Stage
Dr. Mingjiu Chen
CEO 
Functionality

DHVC United States

Life Science and Healthcare Venture Capital Investor
Website:
www.dh.vc
Company Size (Fulltime employees)
Year of foundation
2013
Partnering Objectives
Please specify your partnering goal
Investment
Headquartner in China
Medtech Development Stage
Ali Farahanchi
Managing Director 
Functionality

Genervon Biopharmaceuticals United States

There is a high unmet need for central nervous system (CNS) diseases in the growing aging population. Chronic inflammation is associated with a broad spectrum of neurodegenerative diseases related to aging. Genervon is bringing GM6, a new clinical-stage drug asset, to regulatory approval and commercialization in China for CNS diseases including Parkinson’s disease (PD), Alzheimer’s disease (AD), amyotrophic lateral sclerosis (ALS), Multiple Sclerosis (MS), and other neurodegenerative diseases. Most clinical trials for drugs developed through the traditional single-target drug approach have failed to treat the complex neurological disorders that involve multiple interrelated pathways.

 

GM6 is an innovative first-in-class regulator peptide drug in clinical stage. Genervon Biopharmaceuticals discovered an endogenous embryonic-stage regulator, Motoneuronotrophic Factor (MNTF), and developed from it the pleiotropic drug GM6. GM6 is neither an antibody nor a single-target agonist or antagonist. It is a multi-target regulator which simultaneously acts upon multiple extracellular receptors to modulate a series of signaling pathways mediating inflammation and pro-survival responses in both CNS and immune system. Genervon has validated GM6’s target engagement of multiple targets and druggability. GM6 has been de-risked for toxicity in animal studies and safety in three clinical trials. IND documents filed with the FDA can be used to support regulatory filing in China for clinical trials. Genervon is interested to partner through licensing or merger and acquisition. A complete CMC package is ready for technology transfer.

Website:
www.genervon.com
Partnering Objectives
Assets Information 1
GM6 for Parkinson's disease
Assets Information 2
GM6 for ALS
Assets Information 3
GM6 for Alzheimer's disease
Biotech/Pharma Asset Stage
Slides Deck
(pdf, 1.81MB)
Dorothy Ko
Chief Operating Officer 
Functionality

Idience Co., Ltd.

Idience Co. Ltd. (“Idience’) is a NRDO (No Research & Development Only) company focusing on oncology treatment. The company was established in 2019 by Ildong Holdings Group, a holding company of leading pharmaceutical and healthcare companies in South Korea.

Our first asset, IDX-1197 is a PARP inhibitor for various solid cancers including breast cancer and ovarian cancer. Its ongoing Phase 1a multi-center study showed a promising result. In October 2019, Idience received approval for its initial Investigational New Drug (IND) application from the Korea Ministry of Food and Drug Safety to start a Phase 1b/2a clinical trial for IDX-1197.

Idience is looking for corporate partners to discover and develop oncology therapeutics. We are open to all license-in and license-out partners.
Company Size (Fulltime employees)
Year of foundation
2019, as subsidiary of Ildong Pharmaceutical Co., Ltd.
Partnering Objectives
Please specify your partnering goal
Partner with a Chinese pharma company to develop lead asset for the Greater China region
Headquartner in China
Biotech/Pharma Category
Assets Information 1
IDX-1197||Solid tumors|Global
Biotech/Pharma Asset Stage
Dr. Won Sik Lee
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

Luye United States

Pharmaceutical company
Website:
www.luye.com
Company Size (Fulltime employees)
Please specify your partnering goal
License in
Headquartner in China
Biotech/Pharma Asset Stage
Medtech Development Stage
Dr. Hong Wang
Senior investigator 

Luye pharma China

An international enterprise dedicated to the innovation, ptoduce and selling of innovative drugs
Company Size (Fulltime employees)
Please specify your partnering goal
more RA knowledge
Headquartner in China
Dr Fang Zhang
Senior Business Development Manager 
Ms. Jieyun Hao
HR manager 
Functionality
Mr. Jibo Wang
RA specialist 

Regulaxis 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 osteoarthritis
Biotech/Pharma Asset Stage
Medtech Information 1
Diagnostic companion kit OsteoArthritis
Medtech Development Stage
Slides Deck
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Dr. Matthieu CHAREYRE
Dr. Matthieu CHAREYRE
LinkedIn logo Chief Business Development Officer - Global Pharmaceutical Operations 
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
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
Mr. Raffaello Paolini
R&D Project Manager – East Asian operations development