
Inobrodib
Oral p300/CBP inhibitor in development by CellCentric for relapsed/refractory multiple myeloma.
Last refreshed: 13 May 2026
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inobrodib (also known as CCS1477) is an orally administered small-molecule inhibitor of p300 and CBP, two closely related histone acetyltransferase enzymes that play a central role in transcriptional regulation. By blocking these proteins, inobrodib disrupts gene-expression programmes that cancer cells rely on for proliferation and survival. It was developed by Cambridge-based CellCentric as a targeted therapy for haematological malignancies, particularly relapsed or refractory multiple myeloma — a blood cancer that becomes progressively harder to treat after each line of therapy.
CellCentric's £220m Series B in May 2026 — Europe's largest biotech venture round of the year — is primarily funding inobrodib's clinical programme. The drug is currently in the Phase 2 DOMMINO-1 trial at sites in the UK and US, with a Phase 3 DOMMINO-2 study planned for H2 2026. If Phase 3 succeeds, inobrodib could become the first approved p300/CBP inhibitor, opening a new mechanism class for the estimated 35,000 patients diagnosed with multiple myeloma annually in the UK and US combined.
What is inobrodib and how does it treat multiple myeloma?
What stage is the inobrodib clinical trial at?
Who developed inobrodib and what company makes it?
Why does blocking p300 and CBP help treat cancer?
Written with AI from Lowdown's published reporting. Not individually reviewed by an editor. Updated 13 May 2026. Editorial standards.