July 20 2017 – Personalized cancer therapies are on the horizon thanks to a new genomic cancer research partnership between the Gene Editing Institute of Christiana Care Health System’s Helen F. Graham Cancer Center & Research Institute and the Jerusalem-based biotechnology company NovellusDx.
The Gene Editing Institute has licensed its innovative gene editing technology to NovellusDx to improve the efficiency and speed of NovellusDx’s cancer diagnostic screening tools. With the use of advanced gene editing technology, NovellusDx will be able to identify the genetic mechanism responsible for both the onset and progression of many types of cancer and determine the most effective cancer therapy. NovellusDx will pay royalties to Christiana Care for ten years for the use of its innovative gene editing technology.
A $900,000 grant from the U.S.-Israel Binational Industrial Research and Development (BIRD) Foundation in December 2016 facilitated the Gene Editing Institute-NovellusDx partnership.
“This partnership promises to redefine and transform cancer treatment by speeding progress in breakthrough personalized medicine for many forms of cancer,” said Nicholas J. Petrelli, M.D., the Bank of America endowed medical director of Christiana Care’s Helen F. Graham Cancer Center & Research Institute.
“This work has the potential to change the way cancer treatment is carried out,” said Haim Gil-Ad, CEO of NovellusDx. “Once the genetic makeup of a patient is known, we will be able to immediately test and monitor the effect of a patient’s mutations in live cells and determine the appropriate treatment for that patient.”
Today, genomic sequencing plays an ever-increasing role in cancer treatment, but the functional significance of most mutations found in a patient’s DNA is unknown and so is the effect drugs have on them. NovellusDx will use the gene editing tools to help determine which drug is best for individual patients by recreating the mutations in a test system and then screening a series of known cancer drugs against those mutations to determine their efficacy.
Today, genomic sequencing plays an ever-increasing role in cancer treatment, but the functional significance of most mutations found in a patient’s DNA is unknown and so is the effect drugs have on them. NovellusDx will use the gene editing tools to help determine which drug is best for individual patients by recreating the mutations in a test system and then screening a series of known cancer drugs against those mutations to determine their efficacy.
“The Gene Editing Institute is thrilled to partner with the outstanding scientific team at NovellusDx who are international leaders in the development of personalized medicine and cancer treatment,” said Eric Kmiec, Ph.D., director of the Gene Editing Institute. “We look forward to a long, productive relationship not only in helping to identify effective cancer treatments but also in understanding the mechanism of gene editing in human cells.”
“Combining our state-of-the-art gene editing technology with NovellusDx’s expertise,” Kmiec continued, “will accelerate and improve NovellusDx’s diagnostic testing process, reducing the time it takes to generate the treatment options for the physician and the patient. This will lead to immediate clinical applications and the delivery of precision and personalized cancer therapy at its very best.”
NovellusDx has established a unique approach to identify unknown “driver” gene mutations that can accelerate or facilitate cancer progression. With clinical partners throughout the world, NovellusDx obtains DNA sequence information and creates a personal profile of the genetic mutations from individual patients. Using the licensed gene editing technology from the Gene Editing Institute, NovellusDx will be able to define the impact of each mutation on the activity of signaling pathways of the tumor and suggest the most effective therapy to the patient’s physician.
For more information, see: www.novellusdx.com/news/new_partnership_between_gei_bird_novellusdx
