New Medication Buoys Hope for MS Victims
WASHINGTON — The government approved a drug Tuesday that tries a new method of attacking multiple sclerosis, an incurable disease of the central nervous system that affects 350,000 Americans.
The drug — a monoclonal antibody produced by Cambridge, Mass.- based Biogen Idec Inc. and Irish drug maker Elan Corp. — is known chemically as natalizumab. During clinical trials, it was called Antegren, but in the Food and Drug Administration announcement, the name was changed to Tysabri.
Earlier this month, the drug makers reported that 942 MS patients who took the drug for one year had a 66 percent reduction in relapses, compared with the placebo. That compares with a 30 percent to 35 percent reduction in relapses for products currently on the market. The first-year glance at the study will be followed by second-year results in early 2005.
A second trial looked at MS patients who had one or more relapses with the drug Avonex. Some received Tysabri or placebo along with Avonex. The Tysabri-Avonex treatment reduced relapse frequency by 54 percent, compared with placebo. The most frequent serious side effects were pneumonia, rash, fever, low blood pressure and chest pain.
The company said the MS patients in the second trial had had the disease longer and were harder to treat. Most of those in the first group had been recently diagnosed.
All told, 2,800 patients with multiple sclerosis and Crohn’s disease received Tysabri in placebo-controlled clinical trials. The most frequent side effects were headache, fatigue and inflammation of the nose and pharynx.
Antibodies are proteins that the body’s immune system uses to fight infection. Monoclonal antibodies are made in the lab and act just like people’s own antibodies to attack foreign substances.
The FDA has approved monoclonal antibodies to battle other ailments, including cancer.
But Tuesday’s approval of the monoclonal antibody treatment Tysabri was the first time the government approved the targeted therapy to treat multiple sclerosis. The approval covers intravenous delivery of the drug once a month in a doctor’s office.
“It’s exciting news for patients with MS,” said Dr. David Ross, a supervisory reviewer in the FDA’s Center for Drug Evaluation and Research. “There are no cures for MS, but it does reduce the frequency of relapses … a significant manifestation of the disease.”
Dr. J. Theodore Phillips, an MS expert, said the relapses are devastating for patients who often were perfectly healthy before developing the chronic ailment.
Without warning, a relapse can erase vision, turn a working arm or leg useless or numb feeling below the waist.
In the study Phillips led, Tysabri performed twice as well.
Jardann Moad, who has taken Tysabri since June, said this year marks the first time her MS didn’t flare up in October. Year in, year out, since her diagnosis in 1995, the disease would strike, numbing her right side, causing a leg to drag, anesthetizing most of her body.
“I’ve been feeling great,” said the 46-year-old mother of three who lives near Dallas.