Amphista Therapeutics, based near Cambridge in the UK, designs small molecules that make cancer cells destroy specific proteins using a less common disposal enzyme called DCAF16. Its first drug, for acute myeloid leukaemia, was cleared to start human trials in 2026.
Amphista Therapeutics is a Cambridge, UK targeted protein degradation company whose Targeted Glue degraders deploy E3 ligases beyond cereblon, such as DCAF16, chosen for each target. Its lead programme, AMX-883, is an orally bioavailable, selective DCAF16-mediated BRD9 degrader for acute myeloid leukaemia that releases the differentiation block in a broad AML population, shows in vivo efficacy alone and synergy with venetoclax, and received FDA clearance of its IND application in June 2026 as the first BRD9-targeted therapy for AML. An oral SMARCA2 Targeted Glue degrader targets SMARCA4-deficient tumours including non-small cell lung cancer through synthetic lethality, and a pan-TEAD degrader targets Hippo pathway-driven cancers such as mesothelioma and NSCLC; both are preclinical, with data presented at AACR 2026. The company is registered in England and Wales (number 11119959) with its head office at Granta Park, Great Abington, Cambridge.
Shares Epigenetic drugs (HDAC, DNMT, EZH2, IDH, menin, BET), PROTACs & molecular glues (targeted protein degradation), Non-small-cell lung cancer.
Shares Synthetic lethality approaches, PROTACs & molecular glues (targeted protein degradation).
Shares Synthetic lethality approaches, Epigenetic drugs (HDAC, DNMT, EZH2, IDH, menin, BET), PROTACs & molecular glues (targeted protein degradation), Non-small-cell lung cancer.
Shares Epigenetic drugs (HDAC, DNMT, EZH2, IDH, menin, BET), PROTACs & molecular glues (targeted protein degradation).
Shares Epigenetic drugs (HDAC, DNMT, EZH2, IDH, menin, BET), Acute myeloid leukaemia.
Shares Epigenetic drugs (HDAC, DNMT, EZH2, IDH, menin, BET), Acute myeloid leukaemia.
Shares Epigenetic drugs (HDAC, DNMT, EZH2, IDH, menin, BET), Acute myeloid leukaemia.