Onxeo Appoints Julien Miara as New Interim CEO
Onxeo S.A. has appointed Julien Miara as interim CEO, effective January 3, 2022. Miara, with over 10 years in finance and biotechnology, aims to ensure the company aligns with its strategic plan during the CEO transition. The Board is also seeking a permanent CEO to expedite the development of AsiDNA and enhance international visibility. The company focuses on innovative oncology drugs targeting tumor DNA Damage Response, with promising studies ongoing for AsiDNA™ and OX401.
- Appointment of Julien Miara as interim CEO brings expertise in finance and biotechnology.
- Ongoing clinical studies for AsiDNA™ and OX401 show positive preliminary results.
- Strategic focus on addressing unmet medical needs in oncology.
- Transition period may introduce uncertainty for stakeholders.
- CEO search could distract from development efforts.
The company’s Board of Directors is actively working on recruiting Onxeo’s next CEO who will focus on bringing expeditiously AsiDNA to the patients to respond to their high unmet medical need, develop the rich pre-clinical pipeline such as OX401 and provide
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 first-in-class, highly differentiated DNA Damage Response (DDR) inhibitor based on a decoy and agonist mechanism acting upstream of multiple DDR pathways. Translational research has highlighted the distinctive properties of AsiDNA™, notably its ability to abrogate tumor resistance to PARP inhibitors regardless of the genetic mutation status. AsiDNA™ has also shown a strong synergy with other tumor DNAdamaging agents such as chemotherapy and PARP inhibitors. The DRIIV-1 (DNA Repair Inhibitor-administered IntraVenously) phase I study has evaluated AsiDNA™ by systemic administration (IV) in advanced solid tumors and confirmed the active doses as well as a favorable human safety profile. The ongoing DRIIV-1b extension study is evaluating the safety and efficacy of AsiDNA™ at a dose of 600 mg in combination with the reference chemotherapy, carboplatin -/+ paclitaxel, in advanced metastatic tumors. Preliminary results from both cohorts showed good tolerability, stabilization of the disease and an increase in treatment duration compared to previous treatments. The ongoing REVOCAN phase 1b/2 study evaluates the effect of AsiDNA™ on the acquired resistance to PARP inhibitor niraparib in relapsed ovarian cancer (sponsored by
OX401 is a new drug candidate from platON™, optimized 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 undergoing preclinical proof-of-concept studies, alone and in combination with immunotherapies.
For more information, please visit www.onxeo.com
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