Domainex, a contract research organization, announced a collaboration with Sigma-Aldrich to advance the study of epigenetic proteins involved in cancer and stem cell biology. Through the collaboration, Domainex will use its protein expression technology to produce domains of epigenetic proteins to develop biochemical assays, while Sigma-Aldrich will use the proteins to develop monoclonal antibodies. These tools will help researchers study the function of these important proteins. Funding from the UK Technology Strategy Board will support the work.
Domainex Ark Press Release June 2009 Finaldikheidi
油
Domainex Ltd and Ark Therapeutics have extended their drug discovery agreement. Domainex will continue providing hit-finding and lead optimization services for Ark's therapeutic targets. The companies have worked together successfully for years, combining Domainex's drug design expertise with Ark's disease expertise. Dr. Trevor Perrior of Domainex commented that their collaboration has already achieved breakthroughs against challenging goals, and they look forward to further developing programs to deliver new disease treatments.
Domainex announces the release of the latest version of its LeadBuilder virtual screening platform. LeadBuilder is a proprietary platform developed by Domainex to rapidly identify high-quality small molecule drug leads against novel or difficult protein targets. The latest version includes an expanded database of over six million compounds and software upgrades. LeadBuilder uses target-specific queries to screen compounds and typically achieves hit rates of 1-10%, far better than random high-throughput screening.
Domainex And Pharmidex Announce Drug Discovery Alliancepfallon
油
Domainex and Pharmidex announce a strategic alliance to provide integrated drug discovery services. The alliance will combine Domainex's expertise in hit identification and medicinal chemistry with Pharmidex's strengths in drug metabolism and pharmacokinetics testing. The companies aim to tackle challenging drug targets and believe the partnership will extend their client bases in the pharmaceutical and biotech sectors.
Domainex, a UK-based drug discovery company, won the 2010 Genesis Life Science Innovation and Enterprise Programme of the Year award for its work promoting academic-industry collaborations. Domainex has successfully delivered 3 novel drugs into clinical trials for its clients in the last 4 years. It currently supports drug discovery consortia with groups like Breakthrough Breast Cancer and St George's University of London.
Domainex, a UK-based drug discovery company, won the 2010 Genesis Life Science Innovation and Enterprise Programme of the Year award for its work promoting academic-industry collaborations. Domainex has successfully delivered 3 novel drugs into clinical trials for its clients in the last 4 years using its medicinal chemistry expertise. It currently supports drug discovery consortia with groups like Breakthrough Breast Cancer and St George's University of London.
- Neusentis is a regenerative medicine subsidiary of Pfizer focused on developing cell-based therapies.
- Their portfolio includes collaborations on stem cell-derived retinal pigment epithelial (RPE) cells to treat macular degeneration, and allogenic adult multipotent stem cells to treat inflammatory bowel disease.
- Major challenges for developing and commercializing cell therapies include cell biology and manufacturing complexities, rigorous clinical trial design and supply logistics, and demonstrating a clear business case for pricing and reimbursement.
Domainex has expanded its assay services to include assay development and fragment-based screening using both biochemical and biophysical techniques. It has also launched a new collection of chemical fragments that is more diverse than other commercially available collections. This expansion allows Domainex to screen small molecules against various targets and identify hits using its in silico LeadBuilder technology.
Domainex TSB Funding Awarded For Cancer Programpfallon
油
Domainex, a UK-based drug discovery company, was awarded a 贈250,000 grant by the UK's Technology Strategy Board to support development of a new cancer drug. The drug inhibits two protein kinases, TBK1 and IKK竜, that are important in cancer cell growth. Initial focus will be on breast and ovarian cancers which have poor survival rates. The funding will allow Domainex to hire scientists and advance the drug through preclinical testing towards commercialization with a pharmaceutical partner.
This document summarizes PCT's vision and history as a leader in cell therapy manufacturing. PCT aims to make transformative cell-based therapies accessible to all through providing high-quality and scalable manufacturing services. Over 30 years, PCT has gained unprecedented expertise manufacturing over 20 cell therapy products and treating over 6,000 patients. PCT partners with companies from start-ups to large pharmaceutical companies, and aims to guide clients through the entire development and manufacturing process.
Autologous and Allogeneic Cell Therapy Industrialisation Overcoming Clinical Manufacturing Hurdles Early
A presentation by Chief Operating Officer, Dr Stephen Ward
We have 13 research and development projects within:
Research
Oncology
Respiratory, Inflammation and Autoimmunity
Cardiovascular and Metabolic Disease
Antibody Discovery and Protein Engineering
Pathology
Biopharmaceutical Development
Cell Culture and Fermentation Sciences
Formulation Sciences
Analytical Biotechnology Science
In our final webinar of the MDC Connects Series 2021 | A Guide to Complex Medicines.
This slide deck takes a closer look at overcoming the challenges of scaling up a complex medicine.
Graham Worrall and Emily Port, CPI
Translating Cell Therapies: Academic versus Industry modelnanog
油
This document discusses the differences between academic and industry models for cell therapy clinical trials. Academia focuses on early stage "first-in-human" pilot studies using autologous cell therapies for rare diseases, while industry aims for large-scale allogeneic therapies for prevalent diseases. Key differences include scale, funding, and regulatory pathways. There is a need for more academic Good Manufacturing Practice cell therapy facilities to help translate research into applications, though gaps exist in quality control and commercialization expertise. Increased collaboration and education can help bridge gaps between academia and industry.
Genomics Solutions - Single Target to Whole Genome AnalysisCovance
油
With applied Genomics expertise, global co-location with Central Labs and solutions from biomarker discovery to CDx, our genomics solutions will help make your Precision Medicine drug development a reality.
This document discusses a patented formulation technology from TSRL that can modify the release properties of water-insoluble drugs to provide extended or delayed delivery. The technology is supported by an issued US patent that expires in 2033. Proof-of-concept studies in humans have demonstrated the ability to increase exposure and modulate the pharmacokinetic profile of simvastatin using a delayed release formulation. The technology offers a low-cost option for partners to test formulations and has the potential to improve therapies for conditions that follow circadian patterns or require lower and less toxic doses.
TSRL, Inc. is a preclinical drug development accelerator located in Ann Arbor, Michigan that aims to advance promising compounds for treating severe and drug-resistant infections. The document outlines TSRL's capabilities including analytical testing, pharmacokinetics studies, formulation development, and efficacy modeling. It also discusses funding opportunities through Small Business Innovation Research grants from the National Institute of Allergy and Infectious Diseases as well as other NIH research grants that could support infectious disease drug development.
Our fourth webinar in the MDC Connects Series 2021 | A Guide to Complex Medicines.
This slide deck takes a closer look at alternative delivery for mRNA vaccines.
Helen McCarthy, pHion Therapeutics
An ever-evolving regulatory environment makes navigating gene therapy products through to clinic much more complicated than a traditional biologic. While manufacturing platforms and regulatory requirements for testing of antibodies has existed for decades, gene therapy platforms and their testing requirements are changing rapidly with the progression of products toward commercialization.
The document describes TSRL Inc.'s Technology Accelerator program, which aims to help move therapeutic assets past the "Valley of Death" by providing infrastructure, scientific and business resources, and funding to drive projects from pre-clinical development to an Investigational New Drug application. The accelerator selects potential drug candidates based on criteria to maximize commercialization potential and provides services like project management, drug development expertise, and access to networks to help obtain funding and partners. The goal is to generate necessary data packages and commercialization plans to support projects reaching their next development milestones.
The Cell Therapy Catapult was established to help grow the UK cell therapy industry by providing facilities, expertise, and funding for collaboration between researchers and industry. It has laboratories and teams working on process development, clinical trials, and business development. In its first year it has over 60 staff and is engaged in both small and large collaborative projects. The goal is to deliver life-changing cell therapies and investible projects that help establish UK leadership in this industry.
Targos and AKESOgen form a strategic partnership to provide a comprehensive biomarker service for clinical trials and molecular pathology. The partnership will combine Targos' strengths in companion diagnostics, pathology, and biomarker capabilities with AKESOgen's 14,000 square foot US facility, genetic and molecular expertise. This will allow Targos to expand its suite of services in the US and better serve customers, while supporting AKESOgen's high quality pathology services and establishing a US footprint.
Cell Therapy Manufacturing: Regulations and Facilitieswrtolbert
油
This document discusses the regulatory and manufacturing challenges of cell therapy products. It notes that cell therapies must be aseptically processed but cannot be fully sterilized like traditional drugs. The challenges include controlling differentiation of stem cells into the desired target cell type, developing potency assays, and dealing with variability in biological materials. Manufacturing challenges include developing aseptic processing methods, handling adventitious agents, and scaling up production capacity for either autologous or allogeneic use. Larger centralized facilities face quality oversight and logistical issues, while smaller regional facilities could better concentrate expertise, quality, and handling of incoming/outgoing cells and products.
This document provides an overview and agenda for the 2nd annual conference on drug discovery taking place on March 21st-22nd, 2018 in London. The conference will feature presentations and discussions on:
1) New technologies to improve discovery cycles in chemistry and drug discovery processes, including the role of artificial intelligence and new modalities like PROTACs and antibodies.
2) Advances in small molecule therapeutics from Roche and challenges in validating targets with CRISPR from Epizyme.
3) The role of open access chemical probes from the SGC and how Bayer uses them in drug discovery.
4) How artificial intelligence can transform drug design and discovery efforts at companies like Exscient
Natural products company Hypha Discovery has signed a deal with Domainex to develop novel oncology drugs. Hypha has identified a pipeline of natural products with activity against tumor cell lines, including the HD148 chemical series inspired by compounds from a tropical mushroom. Domainex will use its drug development platform and medicinal chemistry expertise to optimize the HD148 series and deliver an advanced lead molecule and clinical candidate. Both companies look forward to the collaboration advancing Hypha's oncology programs.
Horizon Discovery and Domainex Ltd have collaborated to support Domainex's TBK1/IKK竜 oncology research program. Under the agreement, Horizon will use its isogenic cell lines that model cancer mutations to profile Domainex's lead compounds. This will help identify which patient subgroups will respond and guide medicinal chemistry optimization. The collaboration will help efficiently develop a drug for this cancer target.
Domainex has expanded its assay services to include assay development and fragment-based screening using both biochemical and biophysical techniques. It has also launched a new collection of chemical fragments that is more diverse than other commercially available collections. This expansion allows Domainex to screen small molecules against various targets and identify hits using its in silico LeadBuilder technology.
Domainex TSB Funding Awarded For Cancer Programpfallon
油
Domainex, a UK-based drug discovery company, was awarded a 贈250,000 grant by the UK's Technology Strategy Board to support development of a new cancer drug. The drug inhibits two protein kinases, TBK1 and IKK竜, that are important in cancer cell growth. Initial focus will be on breast and ovarian cancers which have poor survival rates. The funding will allow Domainex to hire scientists and advance the drug through preclinical testing towards commercialization with a pharmaceutical partner.
This document summarizes PCT's vision and history as a leader in cell therapy manufacturing. PCT aims to make transformative cell-based therapies accessible to all through providing high-quality and scalable manufacturing services. Over 30 years, PCT has gained unprecedented expertise manufacturing over 20 cell therapy products and treating over 6,000 patients. PCT partners with companies from start-ups to large pharmaceutical companies, and aims to guide clients through the entire development and manufacturing process.
Autologous and Allogeneic Cell Therapy Industrialisation Overcoming Clinical Manufacturing Hurdles Early
A presentation by Chief Operating Officer, Dr Stephen Ward
We have 13 research and development projects within:
Research
Oncology
Respiratory, Inflammation and Autoimmunity
Cardiovascular and Metabolic Disease
Antibody Discovery and Protein Engineering
Pathology
Biopharmaceutical Development
Cell Culture and Fermentation Sciences
Formulation Sciences
Analytical Biotechnology Science
In our final webinar of the MDC Connects Series 2021 | A Guide to Complex Medicines.
This slide deck takes a closer look at overcoming the challenges of scaling up a complex medicine.
Graham Worrall and Emily Port, CPI
Translating Cell Therapies: Academic versus Industry modelnanog
油
This document discusses the differences between academic and industry models for cell therapy clinical trials. Academia focuses on early stage "first-in-human" pilot studies using autologous cell therapies for rare diseases, while industry aims for large-scale allogeneic therapies for prevalent diseases. Key differences include scale, funding, and regulatory pathways. There is a need for more academic Good Manufacturing Practice cell therapy facilities to help translate research into applications, though gaps exist in quality control and commercialization expertise. Increased collaboration and education can help bridge gaps between academia and industry.
Genomics Solutions - Single Target to Whole Genome AnalysisCovance
油
With applied Genomics expertise, global co-location with Central Labs and solutions from biomarker discovery to CDx, our genomics solutions will help make your Precision Medicine drug development a reality.
This document discusses a patented formulation technology from TSRL that can modify the release properties of water-insoluble drugs to provide extended or delayed delivery. The technology is supported by an issued US patent that expires in 2033. Proof-of-concept studies in humans have demonstrated the ability to increase exposure and modulate the pharmacokinetic profile of simvastatin using a delayed release formulation. The technology offers a low-cost option for partners to test formulations and has the potential to improve therapies for conditions that follow circadian patterns or require lower and less toxic doses.
TSRL, Inc. is a preclinical drug development accelerator located in Ann Arbor, Michigan that aims to advance promising compounds for treating severe and drug-resistant infections. The document outlines TSRL's capabilities including analytical testing, pharmacokinetics studies, formulation development, and efficacy modeling. It also discusses funding opportunities through Small Business Innovation Research grants from the National Institute of Allergy and Infectious Diseases as well as other NIH research grants that could support infectious disease drug development.
Our fourth webinar in the MDC Connects Series 2021 | A Guide to Complex Medicines.
This slide deck takes a closer look at alternative delivery for mRNA vaccines.
Helen McCarthy, pHion Therapeutics
An ever-evolving regulatory environment makes navigating gene therapy products through to clinic much more complicated than a traditional biologic. While manufacturing platforms and regulatory requirements for testing of antibodies has existed for decades, gene therapy platforms and their testing requirements are changing rapidly with the progression of products toward commercialization.
The document describes TSRL Inc.'s Technology Accelerator program, which aims to help move therapeutic assets past the "Valley of Death" by providing infrastructure, scientific and business resources, and funding to drive projects from pre-clinical development to an Investigational New Drug application. The accelerator selects potential drug candidates based on criteria to maximize commercialization potential and provides services like project management, drug development expertise, and access to networks to help obtain funding and partners. The goal is to generate necessary data packages and commercialization plans to support projects reaching their next development milestones.
The Cell Therapy Catapult was established to help grow the UK cell therapy industry by providing facilities, expertise, and funding for collaboration between researchers and industry. It has laboratories and teams working on process development, clinical trials, and business development. In its first year it has over 60 staff and is engaged in both small and large collaborative projects. The goal is to deliver life-changing cell therapies and investible projects that help establish UK leadership in this industry.
Targos and AKESOgen form a strategic partnership to provide a comprehensive biomarker service for clinical trials and molecular pathology. The partnership will combine Targos' strengths in companion diagnostics, pathology, and biomarker capabilities with AKESOgen's 14,000 square foot US facility, genetic and molecular expertise. This will allow Targos to expand its suite of services in the US and better serve customers, while supporting AKESOgen's high quality pathology services and establishing a US footprint.
Cell Therapy Manufacturing: Regulations and Facilitieswrtolbert
油
This document discusses the regulatory and manufacturing challenges of cell therapy products. It notes that cell therapies must be aseptically processed but cannot be fully sterilized like traditional drugs. The challenges include controlling differentiation of stem cells into the desired target cell type, developing potency assays, and dealing with variability in biological materials. Manufacturing challenges include developing aseptic processing methods, handling adventitious agents, and scaling up production capacity for either autologous or allogeneic use. Larger centralized facilities face quality oversight and logistical issues, while smaller regional facilities could better concentrate expertise, quality, and handling of incoming/outgoing cells and products.
This document provides an overview and agenda for the 2nd annual conference on drug discovery taking place on March 21st-22nd, 2018 in London. The conference will feature presentations and discussions on:
1) New technologies to improve discovery cycles in chemistry and drug discovery processes, including the role of artificial intelligence and new modalities like PROTACs and antibodies.
2) Advances in small molecule therapeutics from Roche and challenges in validating targets with CRISPR from Epizyme.
3) The role of open access chemical probes from the SGC and how Bayer uses them in drug discovery.
4) How artificial intelligence can transform drug design and discovery efforts at companies like Exscient
Natural products company Hypha Discovery has signed a deal with Domainex to develop novel oncology drugs. Hypha has identified a pipeline of natural products with activity against tumor cell lines, including the HD148 chemical series inspired by compounds from a tropical mushroom. Domainex will use its drug development platform and medicinal chemistry expertise to optimize the HD148 series and deliver an advanced lead molecule and clinical candidate. Both companies look forward to the collaboration advancing Hypha's oncology programs.
Horizon Discovery and Domainex Ltd have collaborated to support Domainex's TBK1/IKK竜 oncology research program. Under the agreement, Horizon will use its isogenic cell lines that model cancer mutations to profile Domainex's lead compounds. This will help identify which patient subgroups will respond and guide medicinal chemistry optimization. The collaboration will help efficiently develop a drug for this cancer target.
This press release summarizes a collaboration between UCB and Domainex to develop cancer drugs targeting MEK protein. Using Domainex's protein engineering technology, they were able to identify a form of MEK suitable for structural analysis. This provided UCB with high-resolution structural information to design a novel class of MEK inhibitor molecules with potential to treat cancer. The collaboration validated Domainex's technology in rapidly solving challenges in identifying drug targets.
University of Leicester Press release 2016Philip Fallon
油
Dr. Aude Echalier of the University of Leicester won Domainex's Discovery STAR Award to support her research aiming to develop a new treatment for diffuse large B-cell lymphoma. She will work with Domainex to identify drug-like inhibitors of deubiquitinase enzymes using their virtual screening platform, with the goal of obtaining further funding to develop drug candidates. Domainex provides the award to early-stage projects annually to help researchers advance their drug discovery work.
Domainex Press Release For Wt Mpr Final Version (2) (2)dikheidi
油
Domainex, an innovative biopharmaceutical company, announced a collaboration with St Georges Hospital Medical School and the University of Manchester on a new asthma treatment. Domainex will provide over 贈1.5 million in services like lead optimization over two years to help develop a drug candidate for clinical trials. Researchers discovered compounds that inhibit an enzyme triggering asthma. The universities received a 贈4 million grant to advance the research. The collaboration will use Domainex's virtual screening and medicinal chemistry expertise to accelerate developing an anti-asthma drug.
Domainex, an innovative biopharmaceutical company, announced a collaboration with St Georges Hospital Medical School and the University of Manchester on a new asthma treatment. Domainex will provide over 贈1.5 million in services like lead optimization over two years to help develop a drug candidate for clinical trials. Researchers discovered compounds that inhibit an enzyme triggering asthma. The universities received a 贈4 million grant to advance the research. The collaboration will use Domainex's expertise in computational chemistry to accelerate developing an anti-asthma drug.
The East of England is a major center for medical technologies and healthcare companies, contributing 贈500m annually to the economy. It is home to over 400 healthcare companies and 5,000 expert employees. The region contributes 25% of the UK's total R&D spending, three times the national average, and is a global leader in areas like drug delivery, medical materials, diagnostics and nanotechnology due to collaboration between its universities, hospitals, and industry partners. This document provides information on organizations and facilities supporting medical innovation through research, product development, and commercialization in the East of England region.
This document provides information about the "CNS Clinical Trials" conference taking place on September 16-17, 2010 in London. The conference will examine strategies for successful CNS drug development and overcoming challenges in clinical trial design, management, and recruitment. Key topics will include novel cognitive assessment methods, advances in neuroimaging, adaptive trial design, and the use of biomarkers to demonstrate early drug effects in CNS trials. Speakers will include representatives from pharmaceutical and biotechnology companies as well as academic institutions. Attendees will gain insights on improving various aspects of CNS clinical trials from development through regulatory approval. The conference also provides sponsorship and exhibition opportunities for companies to promote their products and services.
Domainex, a biotechnology company, has secured further financing from existing shareholders Longbow Capital and The Capital Fund, as well as new investor Takeda Research Investment. This funding will allow Domainex to advance its internal oncology drug research portfolio and take its novel cancer targets toward corporate collaborations and deals. CEO Eddy Littler welcomed the new investment and said it will help the company further develop its Combinatorial Domain Hunting technology and oncology pipeline over the next few months.
Domainex, a biotechnology company, has secured further financing from existing shareholders Longbow Capital and The Capital Fund as well as new investor Takeda Research Investment. This funding will allow Domainex to advance its internal oncology drug research portfolio and take its novel cancer targets toward corporate collaborations and deals. CEO Eddy Littler welcomed the new investment and said it will help the company further develop its Combinatorial Domain Hunting technology and oncology pipeline over the next few months.
This document is a program for the 3rd annual ADC Summit 2014 conference on antibody-drug conjugates taking place from May 19-21, 2014 in London. The conference will feature presentations from industry experts on topics related to developing antibody-drug conjugates, including payloads, linkers, manufacturing, and clinical trials. Attendees can learn about the latest developments and network with other professionals in the field. A pre-conference workshop on May 21st will focus on early phase development considerations for antibody-drug conjugates to support first-in-human clinical trials.
Dr. Adrian Stevens received his Ph.D. in computational chemistry from the University of Portsmouth. He has since worked for 9 years at a contract research organization specializing in small molecule discovery research and collaborated with pharmaceutical companies. Following a brief time at another company, he joined Accelrys in 2008 and is now a Senior Product Marketing Manager responsible for the Discovery Studio product.
Dyadic International presented on their C1 vaccine technology platform. C1 is a genetically engineered fungal strain that can rapidly produce high yields of proteins for vaccines and biologics. C1 offers advantages over other platforms like CHO cells, including lower production costs, faster production timelines, and the ability to produce various vaccine modalities. Dyadic discussed their rapid strain development process, high productivity data for vaccine antigens, and plans to initiate a Phase 1 clinical trial of their C1-produced COVID-19 booster vaccine called DYAI-100.
This document introduces a new 60 million venture capital fund called CRB Bio II that will invest in early-stage biotech companies. It will be managed by CRB Inverb鱈o, a new venture capital firm created by the founding partners of Cross Road Biotech, a Spanish VC firm with experience investing in 11 biotech companies. The fund aims to generate high returns by leveraging the management team's expertise and network in the biotech industry in Spain.
Life Technologies (now Thermo Fisher Scientific) combines next-generation sequencing, in silico gene design and synthesis, synthetic biology products, and manufacturing capabilities to form a comprehensive synthetic vaccine development workflow.
This document announces the 11th Annual Biosimilars UK conference taking place October 29-31, 2012 in London. It will bring together major pharmaceutical companies, regulatory bodies, CROs, CMOs, and law firms to discuss strategies for competing in the complex biosimilars market. Key topics will include the latest regulatory guidelines, financial viability, patent strategies, approval pathways, legal issues, preclinical/clinical challenges, the roles of the US and European markets, pricing/reimbursement, and pharmacovigilance. The goal is to help participants maximize opportunities in this changing landscape. Major sponsors include Merck Millipore and United BioSource Corporation.
The 10 most trusted vaccine solution providers, 2020Merry D'souza
油
In this edition, The 10 Most Trusted Vaccine Solution Providers, 2020 CIO Look has shortlisted various healthcare organizations which are playing an important role towards the global healthcare system.
American CryoStem Corporation was founded in 2008 to standardize adipose tissue-derived stem cell technologies. It operates FDA-registered clinical laboratories in New Jersey, Hong Kong, and Japan. The company leverages its intellectual property portfolio and clinical platform to create a global network of licensed laboratories, physicians, patients, and researchers. Its products include adult stem cells derived from adipose tissue and characterized for regenerative medicine applications. The company focuses on collaborations to discover, develop, and commercialize new adipose-derived stem cell products and applications.
American CryoStem Corporation is a biotechnology company founded in 2008 that operates FDA-registered clinical laboratories. It has developed a proprietary platform and portfolio of intellectual property focused on collecting, processing, storing, and differentiating adipose tissue and adipose-derived stem cells for regenerative medicine applications. The company's products and services are aimed at allowing individuals to prepare for their current or future regenerative medicine needs by storing their stem cells when they are young and healthy.
American CryoStem Corporation was founded in 2008 to standardize adipose tissue-derived stem cell technologies. It operates FDA-registered clinical laboratories in New Jersey, Hong Kong, and Japan. The company leverages its intellectual property portfolio and stem cell products to create a global network of licensed laboratories, physicians, patients, and researchers. Its research focuses on collaborations to discover, develop, and commercialize adipose-derived stem cell products and applications in regenerative medicine.
1. Press Release
Domainex collaborates with Sigma-Aldrich to advance the study of
epigenetic proteins involved in cancer and stem cell biology
Cambridge, UK, 15th November 2010.
Domainex Ltd., the Contract Research Organization committed to excellence
in drug discovery, today announced a collaboration with Sigma-Aldrich
(Nasdaq: SIAL) that will provide essential tools, including biochemical assays
and monoclonal antibodies, for the study of proteins involved in the rapidly
developing field of epigenetics. These epigenetic proteins regulate DNA
expression and can be critical to cancer and stem cell biology research.
Funding from the UK Government-backed Technology Strategy Board will
support this work.
Under the collaboration, Domainex will use its proprietary Combinatorial
Domain Hunting (CDH) technology, which enables researchers to clone and
express challenging proteins, to produce soluble domains of a number of
proteins that have key roles in epigenetics. Domainex will use those proteins
to construct biochemical assays for the target enzymes, and Sigma-Aldrich
will use the proteins as antigens to raise specific monoclonal antibodies. The
assays and monoclonal antibodies, which will be distributed by Sigma-Aldrich,
will be used by researchers to identify the target proteins and allow their
function to be characterized and studied in detail.
Dr. Eddy Littler, CEO of Domainex, said, The Domainex research pipeline
contains several projects aimed at proteins involved in epigenetics and
cancer. With the support of the Technology Strategy Board we will be able to
develop useful biochemical assays for these targets. We are particularly
excited about our collaboration with Sigma-Aldrich, as it is a leading company
in the development of monoclonal antibodies for commercial use. It is very
rewarding to be able to make a contribution to the study of proteins involved in
epigenetics and disease.
- ENDS -
2. Editors Notes:
About Domainex
Domainex uses unique and proprietary technologies to resolve common drug
discovery bottlenecks facing the pharmaceutical and biotechnology industries in the
post-genomic era. Major discovery 'gaps' exist between the vast amount of genomic
information that is now available, the accessibility of the corresponding proteins for
use in target validation and drug discovery, and the identification of robust hits in a
cost effective manner. Founded in 2002, Domainex is a privately owned company
with laboratories in Cambridge, England, and offices in the London Bioscience
Innovation Centre.
Domainex has developed a number of platform technologies specifically aimed at
enabling biotech or university groups who have exciting new drug targets. Its
Combinatorial Domain Hunting (CDH) technology, which enables it to clone and
express challenging proteins, will deliver protein constructs that are soluble, stable,
and produced in high-yield - thereby opening up the path to high throughput
screening, structural biology, or antibody production.
Domainex has also developed LeadBuilder - a virtual screening approach for
targets which is specifically aimed at identifying hit molecules that are ideally suited
for further development.
Domainexs experienced medicinal chemistry team has a proven track record in
supporting biotech or university groups by providing expertise to take hit compounds
through lead optimization and on to candidate selection. Several compounds arising
from these collaborations are currently in clinical evaluation. Domainex works with
clients on a fee-for-service basis.
In 2010, the company secured investment to advance its own internal drug
discovery pipeline based upon a number of targets in oncology. These targets are
being progressed using Domainexs platform technologies.
For more information see: www.domainex.co.uk or contact:
Joanne McCudden
Head of Business Development
Joanne.mccudden@domainex.co.uk
Tel +44 (0)1993 201 801
About the Technology Strategy Board
The Technology Strategy Board is a business-led executive non-departmental
public body, established by the government. Its role is to promote and
support research into, and development and exploitation of, technology and
innovation for the benefit of UK business, in order to increase economic
growth and improve the quality of life. It is sponsored by the Department for
Business, Innovation and Skills (BIS). For further information please visit
www.innovateuk.org.