Alan Ashworth

World-Renowned Cancer Researcher, Dr. Alan Ashworth, Joins Phoenix Molecular Designs Advisory Board

Retrieved on: 
Thursday, February 4, 2021

SAN DIEGO and VANCOUVER,BC, Feb. 4, 2021 /PRNewswire/ - Phoenix Molecular Designs (PhoenixMD), an industry leader in the development of precise cancer therapeutics focusing on first-in-class RSK kinase inhibitors, today announced the appointment of Dr. Alan Ashworth PhD, FRS to their Advisory Board as a Scientific Advisor.

Key Points: 
  • SAN DIEGO and VANCOUVER,BC, Feb. 4, 2021 /PRNewswire/ - Phoenix Molecular Designs (PhoenixMD), an industry leader in the development of precise cancer therapeutics focusing on first-in-class RSK kinase inhibitors, today announced the appointment of Dr. Alan Ashworth PhD, FRS to their Advisory Board as a Scientific Advisor.
  • His team identified RSK2 using unbiased functional screens in search of novel drug targets for specific breast cancer subtypes.
  • This research launched Phoenix Molecular Designs in 2012, the only company to have developed a first-in-class small molecule against RSK.
  • Moreover, in the same article that highlighted RSK2 as a target for TNBC, Alan also identified PIK3CA as a target for luminal breast cancer.

Circle Pharma Appoints Alan Ashworth, PhD, FRS and Bruce Stillman, PhD, FRS to Its SAB

Retrieved on: 
Wednesday, October 21, 2020

Circle Pharma, Inc., a macrocycle drug discovery and development company focused on intractable cancer targets, has appointed Prof. Alan Ashworth, PhD, FRS and Bruce Stillman, PhD, FRS to its Scientific Advisory Board.

Key Points: 
  • Circle Pharma, Inc., a macrocycle drug discovery and development company focused on intractable cancer targets, has appointed Prof. Alan Ashworth, PhD, FRS and Bruce Stillman, PhD, FRS to its Scientific Advisory Board.
  • Dr. Stillman is the President and CEO of Cold Spring Harbor Laboratory (CSHL) in New York.
  • We are delighted that Alan and Bruce are joining our growing SAB.
  • Inhibition of Cyclin A has been shown to be synthetically lethal in cancers driven by mutations in the Rb pathway.