High-Dose of INTROGENS ADVEXIN gene therapy provides significant survival advantage to head and neck cancer patients in phase 2 study
4/9/2002 San Francisco American Association for Cancer Research Recurrent head and neck cancer patients receiving higher dose of ADVEXIN® gene therapy in one study had a significant survival advantage when compared to a group of patients in another study receiving a lower dose of the drug, according to the results of two Phase 2 studies presented today at the annual meeting of the American Association for Cancer Research. Study results show that, for the first five months of the trial, patients in the ADVEXIN high-dose study were 50 percent more likely to live than those in the low-dose study. ADVEXIN, which combines a proprietary adenoviral vector with the p53 gene, is the lead product candidate of Introgen Therapeutics, Inc. (NASDAQ: INGN). "We are extremely encouraged by these results demonstrating a significant survival advantage in patients who received a high dose of ADVEXIN," said Max W. Talbott, Ph.D., Introgen's senior vice president of worldwide commercial development. "There have been drugs approved to treat cancer that demonstrated a less beneficial survival advantage in clinical trials." Patients receiving high-dose ADVEXIN had a median survival advantage 2.4 months longer (189 days vs. 114 days) than those receiving a low-dose treatment with the drug. Dosing in the low-dose study was 50 times lower than dosing in the high-dose trial. Dosing in the high-dose trial was consistent with dosing in Introgen's current phase 3 studies of ADVEXIN in the treatment of head and neck cancer. Data from the same studies also show a 60 percent improvement [...]