Our story
CellCentric is built on the science of co-founder Azim Surani, Ph.D., of the Gurdon Institute, University of Cambridge. As a pioneer of cell fate control research, Dr. Surani discovered and described an inherited code, beyond DNA, that instructs cell function and fate. It quickly became clear that studying chromatin-related cell fate control mechanisms could yield many unexplored targets for new drug discovery.
We investigated over 50 potential drug targets for new cancer therapies, with multiple early medicinal chemistry programs including against methyltransferases and deubiquitnases. Through this effort, we licensed an arginine methyltransferase program to Takeda Pharmaceuticals.
CellCentric’s research evolved to concentrate on twin transcription co-activation proteins p300 and CBP, which drive the expression of genes important in certain cancers, including MYC and IRF4.
Inobrodib has been evaluated in over 500 patients across Phase I/II clinical studies in both solid tumors and hematologic malignancies. Trial sites are active across the US, UK and EU.
CellCentric was co-founded with one of the pioneers of cell fate control research, Prof. Azim Surani, PH.D of the Gurdon Institute, University of Cambridge.
Prof. Surani discovered and described a code, beyond DNA, that could be inherited and instructs cell fate.
When gene regulation goes awry, cancer can result.
It quickly became clear that studying chromatin-related cell fate control mechanisms could yield many unexplored targets for new drug discovery; enzymes that modify DNA, histones and transcription co-activation factors.
Best knowledge drives the identification of the best opportunities.
CellCentric built a network of research and evaluation relationships with over 25 leading academic research groups worldwide, to identify new opportunities for developing breakthrough treatments.
Through collaboration, multiple targets were prioritized for drug discovery.
CellCentric worked on multiple target validation and early medicinal chemistry programs, including methyltransferases and deubiquitinases. An arginine methyltransferase program was licensed to Takeda Pharmaceuticals.
Chromatin-associated proteins are key in regulating gene expression.
CellCentric’s research evolved to concentrate on twin transcription co-activation proteins p300 and CBP, which drive the expression of genes important in cancer progression, including MYC and IRF4.
First of its kind; novel small molecule inhibitor of p300/CBP.
CellCentric went on to develop a potent and specific small molecule p300/CBP inhibitor, inobrodib. It targets the conserved bromodomain of p300/CBP. Inobrodib is formulated as a capsule taken orally.
Inobrodib is now in Phase II clinical trials.
CellCentric is evaluating the safety and efficacy of inobrodib in clinical trials. The main focus is on multiple myeloma. Studies are active across the US, UK and EU.
