Presentations at 26th EORTC-NCI-AACR Symposium Highlight Champions Oncology TumorGrafts' Ability to Evaluate Immune-Modulating Therapies and Guide Clinical Development Strategies
HACKENSACK, N.J., Nov. 19, 2014 /PRNewswire/ -- Champions Oncology (OTC: CSBR), a company engaged in the development of advanced technology solutions and services to personalize the development and use of oncology drugs, today announced the delivery of two presentations at the 26th EORTC-NCI-AACR Symposium, held Nov. 18-21 in Barcelona, Spain, discussing the creation of an innovative TumorGraft model (ImmunoGraft) specific to immune-modulating therapeutics and benefits of Champions' TumorGrafts® in guiding clinical development strategy.
"There continues to be a need for improved models that enable researchers to better understand the clinical potential of therapeutics early in their development, ideally in the preclinical setting," said Keren Paz, Ph.D., chief scientific officer of Champions Oncology. "The findings presented at EORTC-NCI-AACR continue to demonstrate the advantages of our TumorGraft platform and our ability to create personalized mouse models for the exciting new class of immuno-oncology therapeutics. We look forward to presenting future case studies with our ImmunoGrafts at additional conferences in the year ahead."
In a first study, titled "A humanized mouse model for preclinical testing of molecules targeting immune checkpoints," Champions combined its TumorGraft technology with mice engineered to have a human immune system, creating a more accurate and reliable model for evaluating immune-modulating therapeutics. The resulting model, known as ImmunoGraft, will potentially allow for further understanding of interactions between the tumor and immune system to identify the most active drugs and potentially new drug targets. This presentation was granted the prestige status of abstract in the spotlight in the EORTC-NCI-AACR meeting.
In a second presentation, titled "Screening of Champions Predictive TumorGraft Platform Guides the Clinical Development of the Selective Dual BRAF-EGFR Inhibitor CEP-32496" the company described a case study completed with Teva Pharmaceuticals surrounding the development of a dual BRAF-EGFR inhibitor, CEP-32496. TumorGrafts were used to compare the efficacy of CEP-32496, both as monotherapy and in combination, against three approved therapeutics. Results demonstrated the robust therapeutic effect of CEP-32496 compared to the other therapeutics in colorectal cancer and melanoma models, supporting further development in clinical studies.
About Champions Oncology
Champions Oncology, Inc. is engaged in the development of advanced technology solutions and services to personalize the development and use of oncology drugs. The Company's TumorGraft technology platform is a novel approach to personalizing cancer care based upon the implantation of primary human tumors in immune deficient mice followed by propagation of the resulting engraftments, or TumorGrafts, in a manner that preserves the biological characteristics of the original human tumor in order to determine the efficacy of a treatment regimen. The Company uses this technology in conjunction with related services to offer solutions for two customer groups: Personalized Oncology Solutions, in which results help guide the development of personalized treatment plans, and Translational Oncology Solutions, in which pharmaceutical and biotechnology companies seeking personalized approaches to drug development can lower the cost and increase the speed of developing new drugs. TumorGrafts are procured through agreements with a number of institutions in the U.S. and overseas as well as through Champions' Personalized Oncology Solutions business. For more information, please visit www.championsoncology.com.
Contact:
Media Inquiries
Canale Communications
Ian Stone
Account Director
619.849.5388
[email protected]
SOURCE Champions Oncology
Related Links
WANT YOUR COMPANY'S NEWS FEATURED ON PRNEWSWIRE.COM?
Newsrooms &
Influencers
Digital Media
Outlets
Journalists
Opted In
Share this article