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Advancing a first-in-class LSD1/CoREST degrader and predictive biomarker strategy for glioblastoma

GLIOBREAK is developing BEA-17, a first-in-class small-molecule degrader designed to dismantle the LSD1/CoREST complex that helps glioblastoma evade the immune system and resist current treatments. By pairing this novel immuno-epigenetic therapy with a predictive biomarker strategy, the project aims to identify the patients most likely to benefit, moving a new GBM treatment concept from bench top toward clinical application.

3.27

new GBM diagnoses per 100,000 people each year in US registry data

15 ~

months median survival in adults with GBM

7.1 %

five-year relative survival in US registry data

Why this project matters

  • GBM: median survival was 14.6 months in the pivotal chemoradiotherapy trial; US registry five-year relative survival is 7.1% 1, 2, 3
  • Radiotherapy plus temozolomide has remained a core treatment backbone since 2005 1, 2
  • Preclinical cancer studies link LSD1 activity with suppression of anti-tumour immune signalling 4, 5
  • A clinically validated predictive biomarker for BEA-17 patient selection remains a project development objective 6

Project at a glance

  • Period: 1 May 2026–31 October 2028 • Stage: Preclinical 6
  • Funding: €2.57M • Horizon Europe EIC Transition (top 40 of 611 proposals) 6, 7
  • Grant Agreement: 101292011
  • Drug: BEA-17, first-in-class LSD1/CoREST degrader (FDA Orphan Drug Designation) 6, 8, 9
  • Strategy: Predictive biomarker  designed to identify the patients most likely to respond 6
  • Consortium: Beactica Therapeutics AB (Uppsala) •  three collaborating KU Leuven laboratories (Leuven)

From discovery to clinical readiness

A focused path toward BEA-17 clinical readiness

GLIOBREAK connects single-cell glioblastoma biology with the translational work needed to advance BEA-17 toward clinical testing.6, 10

The project combines mechanism, development readiness, and a predictive biomarker strategy designed to identify the patients most likely to respond in future clinical studies.6

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