Other areas of research include
designing novel therapies based on molecular pathways and identifying predictive biomarkers in patients to design personalized, targeted therapies.
In the future, epigenetic editing could also be used to
design novel therapies by initiating permanent changes to cell biology.
Not exact matches
Researchers at the Medical College of Wisconsin (MCW) have linked a specific protein to the development of post-viral infection asthma, which is the first step in generating a
novel type of asthma
therapy designed to prevent development of post-viral asthma in young children.
«Designing an acoustic diode:
Novel design for brighter, clearer ultrasound images and improve diagnosis and
therapy.»
Our collaborative approach and deep scientific and regulatory understanding of each molecule type helps us shape the best strategy for bringing a
novel therapy to market and
design custom studies and programs that reduce risk and accelerate timelines.
The latest developments in CAR - T translation and manufacturing including alternate gene transfer methods to deliver CARs;
novel gene editing approaches, advances in CAR
design to improve safety and efficacy, and progress in creating an «off - the - shelf» allogeneic CAR - T
therapy.
World Advanced
Therapies and Regenerative Medicine Congress Speaker: Mark Zimmerman, Ph.D., Vice President, Operations and Business Development Presentation: New data on a
novel stem cell combination product for diabetes — development and clinical update Date / Time: May 17, 3:30 PM BST Location: Business
Design Centre, London
A bioengineer in the College of Engineering and Computer Science at Florida Atlantic University has received a $ 141,743 grant from the National Cancer Institute of the National Institutes of Health to develop a
novel biodegradable polymer stent that will be
designed to prevent complications while at the same time serving as a drug delivery system for esophageal cancer
therapy.
He is using this knowledge to help
design novel drugs and combination
therapies to fight TB.
My studies of cancer genomes have led to characterization of multiple pediatric and adult tumor types, to development of methods that identify and characterize changes in genomic heterogeneity, to defining acquired resistance mechanisms to targeted
therapies and to
designing novel, personalized vaccines for individual patients.
The approach is to use clinically relevant tumor models such as patient - derived xenografts (PDXs), as well as humanized and immunocompetent transgenic tumor - bearing mice to
design rational combinations of
novel and emerging cancer
therapies, including tumor - targeting and immune - stimulating
therapies, to ultimately improve treatment outcomes for cancer patients.
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