BridGene Biosciences, Inc., a biotechnology company using a unique chemoproteomic technology to discover and develop small molecules for high value, traditionally undruggable targets, announced a research collaboration agreement with the Peter MacCallum Cancer Centre (Peter Mac), a world leading research, education, and treatment center in Melbourne, Australia. Under the collaboration, Peter Mac and BridGene will establish a drug discovery program harnessing Peter Mac’s ovarian chemoresistance phenotypic screening and BridGene’s proprietary IMTAC™ (Isobaric Mass Tagged Affinity Characterization) Chemoproteomics platform to discover new targets and small molecule drug candidates for the treatment of chemoresistant ovarian cancer.
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The drug discovery program will be led by Dr. Kaylene J. Simpson, Associate Professor and Head of the Victorian Centre for Functional Genomics at Peter Mac, Dr. Elizabeth Christie at Peter Mac, and Dr. Wolf Wiedemeyer, Biology Director at BridGene Biosciences. BridGene will have exclusive rights to develop and commercialize the drug candidates that emerge from the research program. Financial terms of the agreement were not disclosed.
“This collaboration with researchers at Peter Mac represents an important milestone for BridGene to develop a novel drug discovery strategy, that combines phenotypic drug discovery (PDD) and target-based drug discovery (TDD). The new approach will efficiently link new drugs, new targets and diseases to create new treatments, and by doing so further validate the power behind our chemoproteomics technology,” stated Ping Cao, Ph.D., Co-founder and CEO of BridGene Biosciences.
Dr. Cao continued, “Phenotypic screening is a potent drug discovery tool that examines compounds in cellular or animal disease models to find those that cause a desirable change in phenotype of disease-related cells and can lead to the discovery of new compounds to treat disease. However, the researchers face considerable challenges identifying the targets (driving the disease) of the compounds, without which, it is difficult to develop the compounds into drugs. BridGene’s IMTAC™ Chemoproteomics platform combines a carefully designed tagged covalent library of small molecule drug-like compounds, live cell screening and quantitative mass spectrometry to identify the targets that bind to the compounds (obtained from phenotypic screening) in live cells and their relative binding affinity, so as to discover new targets that can drive diseases. We believe combining IMTAC™ with phenotypic screening can lead to fast and efficient discovery of compounds capable of eliciting disease reversal and the identification of the biological targets of those compounds, and by doing so change the treatment paradigm for patients with chemoresistant ovarian cancer and other difficult to treat diseases.”