Mechanism-first
We begin with the biology of cell-cycle regulation and identify the patients most likely to respond before a single trial is designed.
Science & discovery
We translate deep mechanistic science into therapies matched to the biology of each patient's disease — not just to a tumor type.
Mechanism first
Every healthy cell pauses to repair its DNA before dividing. Cancer cells hijack this checkpoint, using WEE1 kinase to survive the stress of rapid, uncontrolled growth.
By selectively inhibiting WEE1, our therapy drives cancer cells past the point of no return — overwhelming their ability to repair and divide — while leaving healthier cells comparatively less affected.
Our principles
We begin with the biology of cell-cycle regulation and identify the patients most likely to respond before a single trial is designed.
A biomarker test is developed alongside the therapy, pairing each patient with the treatment most relevant to their tumor's biology.
An oral, once-daily formulation designed to fit into daily life — not a hospital schedule.
How we match patients
Our companion diagnostic strategy means the right patients are identified from the very first screen.
Cyclin E1 amplification is validated as a predictor of response across our translational datasets.
A simple tissue test at trial sites identifies biomarker-positive patients quickly and consistently.
Eligible patients are matched to the therapy most relevant to the biology driving their disease.
Clinical outcomes continuously refine the biomarker strategy and future trial design.
We are advancing the first oral, non-chemotherapy, biomarker-driven approach for Cyclin E1-positive patients — transforming decades of WEE1 research into a novel targeted therapy option.— Chief Scientific Officer, Zentia Therapeutics