OX401 is the second candidate utilizing Onxeo's proprietary platform of decoy agonists, platON™.
- During optimization, OX401 has demonstrated that it inhibited the DNA Damage Response by acting on PARP proteins.
- In parallel, OX401 activated the STING pathway, a recent and promising field of research in immuno-oncology, which makes it amenable to combinations with immuno- oncology agents such as checkpoint inhibitors.
While the clinical relevance of PARP inhibitors is now well-established, this class still has a number of limiting factors, particularly the relatively rapid onset of resistance. Its decoy agonist mechanism of action positions OX401 as a next-generation PARP inhibitor that should not present these limitations and instead offer a lack of acquired resistance and more specificity to cancer cells.
OX401 was also developed to induce a strong immune response through the activation of the STING pathway, an area of significant interest in immuno-oncology. However, current molecules have experienced challenges, notably in terms of toxicity. OX401 is based on the same decoy agonist mechanism as AsiDNA™, Onxeo’s, which showed good tolerance in , and should trigger a rapid and significant inducing effect of innate immunity against tumor cells.
OX401 is currently undergoing proof-of-concept preclinical studies, alone and in combination with cancer immunotherapies.
Patents has been filed to protect Onxeo's intellectual property rights on OX401 , alone and in combination with cancer immunotherapies.
PARP & DDR Inhibitors Summit 2020
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