Complain about a product or service

FDA Approves Resumed Marketing of MS Drug Tysabri

June 6, 2006

Tysabri • FDA Approves Resumed Marketing of Tysabri, With Restrictions • FDA Panel Considers Controversial MS Drug • Another Death Blamed on Tysabri • MS Drug Tysabri Pulled After Patient Dies • FDA Clears New MS Treatment

The Food and Drug Administration (FDA) has approved an application for resumed marketing of Tysabri, but the multiple sclerosis (MS) drug will be subject to a special restricted distribution program.

Tysabri is used to treat patients with relapsing forms of MS to reduce the frequency of flare-ups. It is supposed to be used alone, not in combination with other immune system modifying drugs, and is for patients who don't respond well to other treatments, FDA said.

Tysabri was initially approved by the FDA in November 2004, but was withdrawn by the manufacturer, Biogen-Idec, the following February after three patients in the drug's clinical trials developed PML, a serious and rare viral infection of the brain. Two of the cases were fatal.

Based on this information, FDA put clinical trials of the drug on hold in February, 2005. FDA allowed a clinical trial of Tysabri to resume in February 2006, following a re-examination of the patients who had participated in the previous clinical trials, confirming that there were no additional infections.

To decrease the possibility of patients developing PML in the future, while also making Tysabri available to appropriate MS patients, FDA consulted in March, 2006 with its Peripheral and Central Nervous Systems Drugs Advisory Committee.

The Advisory Committee recommended a risk-minimization program with mandatory patient registration and periodic follow-up to identify as early as possible any cases of PML that may occur, and to try to determine the reason the infection occurs. In response, Biogen-Idec, submitted to FDA a Risk Management Plan, called the TOUCH Prescribing Program, to help ensure safe use of the product.

Following a thorough review of Biogen-Idec's Risk Management Plan and proposed changes to its original marketing application, FDA determined that Tysabri can be made available under the TOUCH Program with the following main features:

• The drug will be prescribed, distributed, and infused only by prescribers, infusion centers, and pharmacies registered with the program.

• Tysabri will be administered only to patients who are enrolled in the program.

• Prior to initiating the therapy, health care professionals are to obtain the patient's Magnetic Resonance Imaging (MRI) scan to help differentiate potential future multiple sclerosis symptoms from PML.

• Patients on Tysabri are to be evaluated at 3 and 6 months after the first infusion and every 6 months after that, and their status will be reported regularly to Biogen Idec.

Report Your Experience
If you've had a bad experience -- or a good one -- with a consumer product or service, we'd like to hear about it. All complaints are reviewed by class action attorneys and are considered for publication on our site. Knowledge is power! Help spread the word. File your consumer report now.