Cell Line-derived Xenograft (CDX) Mouse Models
Cell-line derived xenograft (CDX) mouse models represent one of the first steps of determining the efficacy of your novel anticancer therapies in an in vivo model
InnoSer’s Cell Line-derived Xenograft (CDX) Mouse Models Services
Cell line-derived xenograft (CDX) mouse models are established from immortalized human cancer cells that are implanted and grown in immunodeficient mice. However, to fully recapitulate the intricacies between the immune system and the rodent tumor microenvironment, humanized models are recommended instead of immunodeficient mice. In comparison to syngeneic mouse models, human cell line-derived xenograft (CDX) models offer you the advantage of working with a mouse model with relevant human cancer target proteins as opposed to rodent proteins.
Therefore, experts at InnoSer recommend the use of CDX models as a first step to evaluate the efficacy of your novel targeted anti-cancer compounds using in vivo models of human cancer. Accordingly, cell line-derived xenograft (CDX) mouse models represent an easy-to-use and relatively inexpensive mouse model with short study timelines (2-4 weeks), offering you a cost-effective alternative to other preclinical screening models. However, for running more advanced studies, InnoSer’s experts recommend performing in vivo studies using patient-derived xenograft (PDX) mouse models, offering you the most clinically relevant in vivo cancer model.
✓ Available as subcutaneous, metastatic, or orthotopic models (follow-up can be also done via imaging methods such as ultrasound).
✓ Both murine and rat cell lines are available.
✓ Complementary biodistribution, microenvironment studies, and PK/PD profiling services.
Developing new, safe, and efficacious anticancer therapies is an extremely intricate process. As a preclinical oncology contract research organization (CRO), InnoSer partners with you to help you navigate the complexities of this research area.
Scientists at InnoSer collaborate with you to develop the most optimal study design to help answer your research questions in the most cost-effective way. With flexible and fast study start times you can perform your research at an accelerated pace. By outsourcing your preclinical oncology studies to InnoSer, you gain access to our in vitro and in vivo oncology drug development portfolio.
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Key Cell Line-derived Xenograft (CDX) Mouse Models Readouts
The People Behind Your Research
Céline Erens, PhD, Immunology Study Director
An expert team led by our immuno-oncology study director, Céline Erens helps you choose the right tools and set up optimal study designs. Curating the preclinical testing of your lead compounds with a deep understanding of the field is your solution to accelerating your drug development.
Yanick Fanton, PhD, Chief Scientific Officer
As Chief Science Officer at InnoSer, Yanick is responsible for all customer studies at InnoSer and takes care of the scientific and technical coordination.
Oncology Board Members
Prof. Dr. Esther Wolfs
A member of InnoSer’s Scientific Advisory Board, Dr. Wolfs is a leading researcher in stem cell therapy. Currently a professor at the University of Hasselt, Ester uses stem cells in anticancer therapy and as a model to study Charcot-Marie-Tooth disease type 1A.
MD, PhD Marije Slingerland
A member of InnoSer’s Scientific Advisory Board, Dr. Slingerland from Leiden University Medical Center focuses on clinical trials in gastrointestinal cancer and in head and neck cancer, particularly on intratumoral immune parameters.
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AAALAC Accreditation
InnoSer has earned the AAALAC accreditation, demonstrating our commitment to responsible animal care and use. AAALAC International is a nonprofit organization that promotes the humane treatment of animals in science through voluntary accreditation and assessment programs. Our accreditation is valid for three years, incl. 2023. Read more about the AAALAC accreditation programme here.
Animal Welfare
The 3Rs impact everything from policy and regulatory change to the development and uptake of new technologies and approaches. This is why InnoSer has ongoing commitment and monitoring of these processes. The steps we practice maximize our ability to replace, reduce and refine animal involvement and facilitate our commitment to these principles when it comes to research and drug development.
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