Onxeo to Present New Preclinical Data Highlighting AsiDNA™’s Ability to Fight Tumor Resistance and Protect From Anticancer Treatment Toxicity at AACR Annual Meeting 2022
Onxeo announces new preclinical data for AsiDNA™ ahead of its presentation at the AACR Annual Meeting 2022 from April 8-13, 2022. The findings demonstrate that AsiDNA™ can effectively prevent resistance to tyrosine kinase inhibitors in lung cancer models, showcasing a potential therapeutic avenue. Additionally, it protects healthy cells from the toxic effects of various anti-cancer treatments while enhancing DNA repair in healthy cells. The oral session is set for April 10, and a poster session for April 12, confirming AsiDNA™'s promising role in oncology.
- AsiDNA™ prevents resistance to tyrosine kinase inhibitors, indicating a breakthrough in lung cancer treatment.
- AsiDNA™ shows efficacy in protecting healthy cells from anti-cancer treatment toxicity.
- The upcoming presentations at the AACR Annual Meeting offer visibility and validation of AsiDNA™'s potential.
- None.
- AsiDNA™ proven to overcome resistance to tyrosine kinase inhibitors in lung cancer models
- AsiDNA™ proven to protect healthy cells when combined with conventional antitumor treatments
The oral presentation will describe how AsiDNA™ efficiently prevented the emergence of resistances to tyrosine kinase inhibitors in several models of targetable oncogenic addiction and will point to the therapeutic opportunity of combining AsiDNA™ and TKI (tyrosine kinase inhibitors) to overcome resistance in a clinical setting. These data were obtained within the framework of the collaboration with Pr.
The poster presentation supports AsiDNA™’s potential to protect healthy cells from toxicities of several anti-cancer treatments. When combined with different anti-cancer treatments (Carboplatin+/-Paclitaxel in long-term treatment, Radiotherapy, Doxorubicin, PARP inhibitors), AsiDNA™ induces its nuclear target engagement only in dividing cells, while preserving healthy non dividing cells. In addition, in certain proliferating healthy cells, AsiDNA™ induces a stop in their division or boosts their DNA repair activity, thus protecting them from the toxic effects of anti-cancer treatments. These data were obtained in in vivo and in vitro models within the framework of the collaboration with Pr.
Wael Jdey, Preclinical Lead of
Date/ Time:
To read the abstract: DNA repair-interfering molecule AsiDNA® overcomes resistance to tyrosine kinase inhibitors in lung cancer
Poster Session: PO.ET04.02 – DNA Damage Response and Repair
Date/ Time:
To read the abstract: AsiDNA® treatment protects healthy cells from anticancer treatment toxicity
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Full-year 2021 results:
Thursday, April 7, 2022 (before market opening)
About
platON™ is Onxeo’s proprietary chemistry platform of oligonucleotides acting as decoy agonists, which generates new innovative compounds and broaden the Company’s product pipeline.
AsiDNA™, the first compound from platON™, is a highly differentiated, clinical-stage first-in-call candidate in the field of DNA damage response (DDR) applied to oncology. Its decoy and agonist mechanism acting upstream of multiple DDR pathways results in distinctive antitumor properties, including the ability to prevent or abrogate tumor resistance to targeted therapies such as PARP inhibitors and strong synergy with tumor DNA-damaging agents such as radio-chemotherapy. AsiDNA™ is currently in combination clinical trials in difficult-to-treat solid tumors.
OX401 is a new drug candidate from platON™, designed to be a next-generation PARP inhibitor acting on both the DNA Damage Response and the activation of immune response, without inducing resistance. OX401 is currently being optimized and is 0undergoing preclinical proof-of-concept studies, alone and in combination with immunotherapies.
For further information, please visit www.onxeo.com.
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