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Supreme Court Denied Certiorari

January 12th, 2009 | Posted by Kerry Donahue
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On behalf of CareToLive I must share with you the news that the United States Supreme Court has denied Cert to our case, which means they have chosen not to review the matter.

Such a ruling does not mean that our arguments were without merit, it merely means the Court has determined that it is not important enough for them to spend their judicial resources on at this particular time.

It is possible we could be before the Supreme Court again in the future for several reasons:

1) None of the merits on the underlying claims made by CareToLive, including the fact that the FDA acted capriciously when they denied approval to Provenge on May 8, 2007 have been decided. Those claims will become ripe when a “final decision” is made on Provenge. The original case was dismissed without prejudice in the lower Court which means we can again file a new complaint.

2) We also currently have pending in the Southern District of Ohio the FOIA Complaint that the FDA received a stay on until May. In May the case will become active again and the Court has already ordered the FDA to produce documents.

Also remember that CareToLive still has a duly filed Citizen Petition pending at the FDA. While Jesse Goodman and Andrew von Eschenbach have chosen to ignore it to date, each new commissioner, whether interim or finally appointed, will have the opportunity to review the petition if and when it comes to their attention (if it has not already). There is new hope with each new commissioner.

Also, a friend of CaretoLive filed an appeal at HHS of the NCI decision to redact portions of the Scher e-mail received in an earlier FOIA request, which we await a decision on.

While we are upset about the loss, because the hope was to speed Provenge to the patients who so badly need it as soon as possible, we are far from being done with the ongoing fight.

While much work is done behind the scenes, please know that not a single day goes by where CareToLive members, supporters and its many friends are not taking action in some manner or another to try to speed Provenge to market so that the patients can benefit by it and the new era of immunotherapy treatments for cancer can be ushered in. This is done by continuing to spread the word among our citizens, lobbying important people in Washington within and outside of Congress, working to gain the interest of and assist media and documentary film makers as well as “educating” the FDA (new and old). The delay of Provenge has needlessly delayed the advance of science and shortened the life of many late stage cancer patients who passed without the hope that Provenge might have brought to them, but their memories live on and with us, as we continue to seek justice and reform at the FDA.

We also extend a very special thanks to those at the Abigail Alliance, Accelerate Progress, PHEN, Cancer Cure Coalition and other advocacy groups that are constantly working for the cause and share similar goals to ours.

We are not alone in this fight and continue to ask everyone reading this to continue to spread the word of Provenge. If a weekend arrives and you have not shared the story with someone during that week then write a letter, mail it and tell the story to someone else.

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Death by Wall Street - Rampage of the Bulls
Provenge is approved!

    Provenge has been approved! Thank you to all who helped achieve this important milestone for cancer patients.
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WHATS GOING ON

This Is An Emergency!

We rallied outside the FDA building in Rockville, Maryland on September 18th. Now there are buses riding around Rockville and Washington, D.C., further protesting the shenanigans that took place inside the FDA building, as well as outside.

The FDA has gotten caught up with Wall Street. While it is supposed to be busy with evaluating food and drugs, its employees just can't keep their eyes off the money. So that is how decisions are being made these days.
WE'LL BE BACK

These people traveled from all across the country to protest outside the FDA Building in Rockville, Maryland. The FDA has stopped a safe and effective treatment from getting to men who need it now. The treatment is called Provenge and it treats men who have late stage prostate cancer.

The FDA appointed a panel of experts to help it decide on the safety and efficacy of Provenge. That panel voted 17-0 that Provenge was safe. And it voted 13-4 that Provenge showed substantial evidence it worked. And yet the FDA delayed it. Now it could be a year, a year and a half or it could be three years. It could be forever.

These people will keeping coming back to Rockville and they hope others will join them until the courts, the FDA, Congress or somebody does something about this travesty.