Onxeo Announces 10th Positive DSMB Recommendation to Continue Livatag® ReLive Phase III Trial in HCC
|Paris (France), May 23, 2017 – 6.00 pm CEST – Onxeo S.A. (Euronext Paris, NASDAQ Copenhagen: ONXEO), a clinical-stage biotechnology company specializing in the development of innovative drugs for the treatment of orphan diseases, in particular in oncology, today announced that the company has received the 10th unanimous recommendation from the Data Safety Monitoring Board (DSMB), to continue without modification the Phase III study of Livatag®, ReLive, in patients still undergoing treatment. The DSMB is an independent European board of experts that monitors the blind tolerability data from the study.
ReLive is an ongoing international, randomized Phase III trial designed to evaluate the efficacy of Livatag® in patients with advanced hepatocellular carcinoma (HCC) after failure or intolerance to sorafenib.
The Relive study protocol involved the recruitment of approximately 400 patients, divided into three arms: two Livatag® treatment arms at 20 and 30 mg/m2 every 4 weeks intravenously for 6 hours, until progression or intolerance, and a comparative arm of patients receiving the best available treatment chosen by their physicians. All patients under the protocol have been randomized since the end of January 2017.
“As we approach the key milestone of ReLive’s preliminary results, we are once again very encouraged by the positive recommendations of the DSMB that confirm Livatag®‘s acceptable tolerance profile in terms of safety and side effects. Livatag® aims to treat a challenging pathology, patients with advanced HCC. This product candidate represents a potential new and innovative therapeutic option for patients suffering from this orphan and resistant cancer, and could become a potentially impactful catalyst for the Company,” commented Judith Greciet, CEO of Onxeo.
As per study protocol, the DSMB examines blind tolerance data from the ReLive trial twice a year. However, the DSMB does not receive any data that may enable an assessment of the efficacy of Livatag®.
Preliminary efficacy results from ReLive are expected by mid-2017.
Onxeo is a biotechnology company developing innovative drugs for the treatment of orphan diseases in oncology, driven by high therapeutic demand in one of the fastest growing segments of the pharmaceutical industry.
Learn more by visiting www.onxeo.com
This communication expressly or implicitly contains certain forward-looking statements concerning Onxeo and its business. Such statements involve certain known and unknown risks, uncertainties and other factors, which could cause the actual results, financial condition, performance or achievements of Onxeo to be materially different from any future results, performance or achievements expressed or implied by such forward-looking statements. Onxeo is providing this communication as of this date and does not undertake to update any forward-looking statements contained herein as a result of new information, future events or otherwise. For a discussion of risks and uncertainties which could cause actual results, financial condition, performance or achievements of Onxeo to differ from those contained in the forward-looking statements, please refer to the Risk Factors (“Facteurs de Risque”) section of the 2016 Reference Document filed with the AMF on April 24, 2017, which is available on the AMF website (http://www.amf-france.org) or on the company’s website (www.onxeo.com).