Oncodesign
announced today that the company has acquired exclusive commercialization rights to distribute the world’s most comprehensive collection of human colorectal cancer models directly developed from patient’s tumors. Oncodesign’s clients can now access the entire collection to evaluate therapeutic compounds in house or to carry out preclinical studies with Oncodesign. This new collection has integrated Oncodesign’s Chi-Mice(R) platform, designed to provide preclinical models from human samples. The Chi-Mice(R) platform includes both reconstituted human immune system models on NSG/NOG mice and models xenografted with patient-derived tumors.
“This collection is the result of a five year research program, and is the most comprehensive worldwide in terms of the range of genetic heterogeneity and characterization. It marks a breakthrough in the evaluation of colorectal cancer therapies,” explained Philippe Genne, president and CEO of Oncodesign. “The CReMEC collection ensures low-passage experimental models to fit the clinical reality. This is all the more relevant since preclinical research usually relies on cell lines that may be many years old, grown in tissue culture and then grafted onto mice. Cell lines may drift into different genetic profiles and are not reliable enough to evaluate anticancer therapies.”
CReMEC brings together skills from world-class French institutes, three pharmaceutical companies, and Oncodesign
as project leader. The EUR 5.4 million program has been developed to meet industrial requirements and strict guidelines were observed from conception to characterization. A full range of characterization is available with each model. Clinical, molecular, pharmacological and histological data have been collected and gathered in a dedicated database, in parallel with a biobank.
Oncodesign says the consortium is considering the development of a dedicated national platform. The challenge is to provide patient-derived cancer models for any cancer pathology to meet unsatisfied needs in cancer research.
Unifying Industry to Better Understand GCP Guidance
May 7th 2025In this episode of the Applied Clinical Trials Podcast, David Nickerson, head of clinical quality management at EMD Serono; and Arlene Lee, director of product management, data quality & risk management solutions at Medidata, discuss the newest ICH E6(R3) GCP guidelines as well as how TransCelerate and ACRO have partnered to help stakeholders better acclimate to these guidelines.