Onxeo S.A. (CPH:ONXEO) (Paris:ONXEO), a clinical-stage biotechnology company, announced on Thursday the start of its proof-of-concept preclinical phase for its new optimised drug candidate, OX401.
Results of these studies are expected by early Q4 2019.
According to the company, OX401 was designed by capitalising on Onxeo's expertise of oligonucleotides acting as decoy agonists and exhibits original properties. During optimisation, 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.
OX401 is the second candidate utilising Onxeo's proprietary platform of decoy agonists, platoon.
A comprehensive patent has been filed for OX401 to protect Onxeo's intellectual property rights on this product, alone and in combination with cancer immunotherapies, until 2039.
Preclinical proof-of-concept results showing OX401 efficacy, alone and in combination with immunotherapy treatments, are expected early in the fourth quarter of 2019.
Onxeo develops oncology drugs targeting tumour DNA-binding functions through unique mechanisms of action in the field of DNA damage response (DDR).
Relay Therapeutics wins FDA breakthrough status for zovegalisib in breast cancer treatment
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Valneva and Instituto Butantan launch pilot chikungunya vaccination campaign in Brazil
Lupin launches Dasatinib tablets in US market
WuXi Biologics enters into licence and research service agreement with Vertex Pharmaceuticals
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Astrazeneca Imfinzi perioperative regimen gains positive EU CHMP opinion in early gastric cancer
I Peace generates human iPS cells from NKT cells and offers them for research use
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
AstraZeneca agrees obesity and type 2 diabetes collaboration with CSPC
Ascletis Pharma Inc reports topline results from Phase III open-label study of denifanstat
Innovative Molecules GmbH completes Phase 1 clinical development programme for adibelivir
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA