BioVex Inc Begins Dosing Patients in Phase II Clinical Trials of OncoVEXGMCSF in Malignant Melanoma and in Head and Neck Cancer
2/14/2006 Cambridge, MA press release NewsWire Canada (ww.newswire.ca) BioVex Inc, a leading developer of advanced biologics for the treatment of cancer announced today that the first patients in its phase II clinical trials of OncoVEXGMCSF in malignant melanoma and in head and neck cancer had received their initial doses of the therapeutic treatment. The melanoma trial is a 50 patient multi-center study. The first dosing took place at the Mary Crowley Medical Research Center, Dallas, Texas. The Principal Investigator is Dr John Nemuniatis. The primary endpoint of the study is tumor response rate with secondary endpoints including time to disease progression and median survival time. The head and neck cancer trial is a 16 patient open label study in combination with chemoradiotherapy. It is being carried out at the Royal Marsden Hospital in London (UK). The first patient in this trial has recently completed the seven week dosing regime. The Principal Investigator is Dr Kevin Harrington of the Institute of Cancer Research. The end point of the trial is to assess the safety of OncoVEXGMCSF combined with chemoradiotherapy, and the potential of OncoVEX as neoadjuvant therapy in the treatment of head and neck cancer. Preliminary results from both trials will be available in late 2006. OncoVEX GMCSF is the first in a new class of oncolytic virus that selectively kills tumor cells. In addition it induces tumor cells to secrete GMCSF, to enhance tumor destruction. OncoVEX GMCSF has completed a Phase I/II study in several solid tumors including breast cancer, [...]