Only where the gene is gone
In human tumour cells that still had a working SMAD4, blocking the two signals changed nothing we could measure. In cells that had lost it, the cells became far less resistant to chemotherapy.
For people with cancer of the oesophagus, stomach, pancreas or bowel whose tumour lacks the gene SMAD4.
01 The problem
Surgery can take the first tumour away. What takes lives is the spreading: cancer cells that travel through the body and grow into new tumours elsewhere.
02 What comes after
Four cancers
50 in 100live less than ten months.
People whose cancer had spread, across 13 cancer types: more than a million patients in the United States, 1992–2019. Those with cancer of the pancreas, the oesophagus or the stomach are among the most likely to die of it. Mani et al., Nature Communications, 2024.
03 What we do
Who it can help
The drug is the smallest working part of an antibody, a VHH. It blocks two signals, BMP2 and BMP4, which in a tumour that has lost SMAD4 are no longer held back. In 40 patients’ tumours we examined, 9 in 10 carried raised BMP2 or BMP4; eight of the 40 had lost SMAD4, and all eight carried raised levels.
04 What it does
Twenty-eight days of treatment, in mice carrying a human tumour that had lost SMAD4. The antibody on its own slowed growth against saline; together with chemotherapy it slowed further.
Tumour size at day 28
In human tumour cells that still had a working SMAD4, blocking the two signals changed nothing we could measure. In cells that had lost it, the cells became far less resistant to chemotherapy.
Over the whole 28 days. Chemotherapy damaged the gut lining; adding the antibody did not make that worse.
Labelled antibody was at the tumour within half an hour, and could still be found there a day later. Three mice.
Results in mice, not in people. Published in Cellular Oncology in 2022 and free for anyone to read. Only studies in people can show whether it works in humans.
05 Where it stands
Not a bright idea from last year. One question, followed from the laboratory bench to a molecule that is now being made ready for the clinic.
Results in mice do not always carry over to people.
Why do tumours that have lost the gene SMAD4 behave so much worse? The answer turned out to be two growth signals, BMP2 and BMP4, that nothing holds back any more.
The cell and mouse results appeared in Cellular Oncology, free for anyone to read and check — including every number on this page.
A company, so that the work can leave the university and be made ready for patients rather than for the next paper.
Not yet in people. No study has started, and the drug is not available to anyone.
Longer in the body, the right patients, safety in animals. Only once those three are done can a first study be asked for.

06 For patients
This is research. It is not yet a treatment.
Your own doctor is the right person to talk to about treatment. You are welcome to write to us all the same.
07 The people
Founder · CEO and CSO
Almost20 yearsof her research behind this drug.
COO, business development
CFO
Legal
Senior scientist