The group will ask the FDA to immediately reconsider its flawed decision on Provenge, among others, and approve this new therapy for immediate use by late-stage prostate cancer patients with no viable alternatives. This new immunotherapy has already been endorsed by an FDA-appointed panel of experts who unanimously (17-0) determined it to be safe for its intended use. Further, the panel voted 13-4 in favor of the 'substantial evidence of efficacy' of Provenge, meeting the statutory requirements for immediate FDA approval. Never in its history had the FDA overturned a positive panel recommendation to deny terminal patients their right to live.
"It has become very clear over the past few years that the FDA has instituted a decelerated approval process for cancer therapies, in stark opposition to Congress' intent in legislating for accelerated approval pathways," said Scott Riccio, founding member and advocate for A Right To Live. The Wall Street Journal lamented this problem back in 2005, noting:
"The problem here is the FDA's unethical--and let us stress, unscientific--placebo-controlled trials, in which a subset of study patients are knowingly denied the new treatment and in some cases denied access to any active treatment at all. This may be moral with an antihistamine; it's certainly not with treatments for a terminal disease. What's more, it's entirely unnecessary. We already know what happens to most cancer patients who don't get treated. They die." (Wall Street Journal, March 24, 2005)
"There has never been such an incredible, irrational and unjustifiable denial of the rights of dying patients by such a dysfunctional agency," according to Mr. Riccio. "Approximately 27,000 men will die this year alone from late-state prostate cancer and tens of thousands of other cancer patients will lose their own fights against cancer this year while they wait in vain for new therapies to make their almost ten-year march from discovery to FDA review. We believe patients have a right to live. We're not asking for the FDA to forego scientific review, we're asking the Agency to catch up to the science that already exists and use it to approve and monitor these lifesaving new therapies while patients and their doctors get informed access to them. We hope that if the FDA continues to abdicate its duty to patients, Congress will make the necessary inquiries and legislative changes to reinstate a true accelerated approval process for them."
Patients, doctors, advocates, and other interested parties should visit
A Right To Live Supporters to Rally for FDA Reform and Call for Congressional Action Provenge NOW