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eADMET is an expert in the creation of customised computational models for the prediction of ADME/Tox properties of small drug-like molecules. eADMET’s modular approach combines proprietary and selected external algorithms to create customised prediction models (with integrated error estimation) for clients and partners from the pharmaceutical and biotechnology industry.

eADMET’s product portfolio includes:

1. OCHEM - a public accessible reference system and database
2. Validated models for precise prediction of various ADME/Tox parameters
3. User-friendly customized model solutions for specific customer needs
4. Expert consultancy services with respect to model application and interpretations.

New developments include chemogenomic methods and methods for in vitro to in vivo correlations to address toxicity prediction within drug discovery and REACH.

eADMET was founded as a result of GO-Bio project awarded to Dr Tetko with a financial support from High-Tech Gründerfonds (HTGF) and Bayern Kapital. it is a spinout from Helmholtz Centre, Munich.

Bioversys AG is a privately held Swiss biopharmaceutical company located in Basel that focuses on research and development of new drugs and compounds, which switch-off drug resistance within bacterial pathogens and restore the efficacy of approved antibiotics. Spun out of the ETH-Zurich in 2008, we have profound technological expertise that is based on solid IP.

Genticel is a clinical stage biopharmaceutical company that develops multivalent vaccines for patients infected with Human Papillomavirus (HPV). Till date, the company has raised EUR 27 Mio in funding.

Current investors include Edmond de Rothschild Venture Partners, Innobio Fund, IDInvest (Allianz) and Amundi. 

Our lead investigational vaccine, ProCervix, has successfully finished a very positive data-rich Phase Ib trial on 47 HPV16 and/or 18 infected women. ProCervix is the first therapeutic vaccine offering a solution to the more than 93 million women worldwide already infected with HPV 16 and/or 18 before the appearance of high grade neoplasia. This very large population, exposed at high risk to develop cervical cancer, is only now becoming accessible thanks to new screening guidelines prescribing first line HPV-based testing.

A large survey of prescribers and a Market Access Study predict overwhelming acceptability and a very large market potential.

Genticel wants to take ProCervix into Clinical Phase II and further develop our second product, a heptavalent therapeutic HPV vaccine, up to clinical stage.

To do this, we intend to raise additional capital from our current and selected international investors. 

CEVEC commercializes an innovative platform technology for the production of vaccines and biopharmaceuticals in human cell lines.  

CEVEC’s CAP cells hold high promise for a best-in-class production system for viral vaccines, such as hCMV, Influenza and others, as shown by a recent case study. Compared to leading other cellular production systems (like MDCK) CAP demonstrated outstanding results in view of virus yield, extreme short production cycles and minimal media consumption. CEVEC’s CAP system is suspension based and serum free offering the best starting point for new vaccine production approaches with excellent upscaling possibilities. Being the only remaining independent supplier for human production cell lines, the company sets out to repeat the growth story of Crucell B.V., recently acquired by Johnson & Johnson for 2.4 Bn US$. 

Feasibility studies further demonstrated CAP being a versatile virus production platform with a broad susceptibility for various human-pathogenic human viruses. Commercially significant targets include hCMV, RSV, Influenza, Polio, Measles, AAV, Adenoviruses, Lentiviruses and others. Several lead projects have been identified and planned, including the first human platform for hCMV, together with its partner Vaccine Project Manager, Hannover, Germany.

CEVEC is underway to close another 7-10 Mio. EUR venture round. This investment will be used to push the vaccine lead projects, such as hCMV within 3 years to clinical phase I/IIa results and manage a broad roll-out of its vaccine production technology in order to maximize its company exit value by 2015. Venture investors are still invited to participate in an exciting low-risk and high return growth story. For further information, please click here: www.cevec.com

Immunovaccine is a biotechnology company focused on the application of its novel vaccine delivery platform to the development of vaccines for cancer therapy and infectious diseases. The Company’s DepoVax™ platform is a patented lipid delivery system that presents antigens plus adjuvant to the immune system for a prolonged period and has the potential to enhance immune responses. Immunovaccine has advanced its platform technology and proprietary cancer vaccine into Phase I clinical trials and has demonstrated both safety and immunogenicity potential. Immunovaccine is also capitalizing on the broad potential of its delivery platform by creating new DepoVax-based vaccines through multiple development collaborations. In addition to the Company’s human health vaccine strategy, it continues to capture value from animal health vaccine applications. Immunovaccine has several key partnerships in the animal health sector including an agreement with Pfizer Animal Health, which has licensed the Company’s delivery technology platform to develop vaccines for livestock.