
The drug Benlysta, developed by Human Genome Sciences (HGS) in Rockville, Md., is promising, particularly for African American women, who are three times more likely than white woman to develop the disease, experts say. Additionally, black women tend to get the disease at a younger age and have more severe symptoms than their white counterparts.
Lupus is a chronic and sometimes fatal autoimmune disorder that affects more than 1.5 million Americans, mostly women of childbearing age, rendering some disabled. According to the Lupus Foundation of America, patients can develop fatigue, cardiovascular disease, kidney disorder, kidney failure, arthritis and rashes.
"The findings are remarkable," says Dr. Nathaniel Neal, a clinical practicing rheumatologist at the Valerius Medical Group in Long Beach, Calif. "It's the first drug to significantly impact the course of the disease. This is a breakthrough treatment."
Dr. Neal, who has been working to treat lupus patients for 26 years, says the most exciting part about Benlysta is that it allows doctors to minimize the dose of steroids, which lead to massive weight gain, high blood pressure, diabetes and other side effects in patients. "We now have one agent that really has been shown to be effective with minimum side effects."
Benlysta, given by monthly infusions, is generally well tolerated, according to a 52-week study of 865 Asian, Eastern European and South American patients. The medicine works by inhibiting the B-lymphocyte stimulator, which produces B blood cells that help the body fight infection. In lupus, elevated levels of B-lymphocyte stimulator are believed to produce antibodies that attack and destroy the body's own healthy tissue.
Findings from the trial showed that 57.3 percent of patients on a higher dose of Benlysta and 51.7 percent of those on a lower dose had a meaningful improvement in their symptoms, compared with 43.6 of those taking a placebo.
Benlysta has yet to be approved. HGS, which is working to develop and market the drug with GlaxoSmithKline, will apply for approval later this year.
Tomiko Frasier Hines, a board member and spokeswoman for the National Lupus Foundation of America in Los Angeles, is optimistic about the potential bright spot for lupus patients. In the past, clinical trials conducted by other drug companies have all but failed in their efforts to develop a new medicine to treat the disease.
"It's very hopeful," says Hines, whose sister died in March after a 12-year battle with lupus. "There hasn't been a new medication approved in years. I'm sure that everyone is quite pleased with the news."

Comments: (26)
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By: John Lindsay on 9/01/2009 2:48PM
"particularly for African American women, who are three times more likely than white woman to develop the disease, experts say"
JL: Lupus is RARE on the continent of Africa.
Hence, why are the numbers like they are in America?
There's an unknown factor that's not "race"-related.
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By: Claude Parker on 9/01/2009 2:49PM
Wow! Hopefully this treatment will drastically reduce the pain for Lupus patients. They suffer so much. My wife has had it for 30 years. I just made a film on how they deal with it. To them discribe what they go through is gut-wrenching. You can see it at www.claudeparker.com/lupus.php Thanks for sharing this story, Lynette.
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By: biglisa on 9/01/2009 2:00PM
i think this is great. i recently lost my best friend. and then not even a year later we lost her daughter any kind of help that they find is wonderful they both suffered so much. i dont ever wanna this to happen to another family.
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By: selah65 on 9/01/2009 2:51PM
This is wonderful news!! I lost my mom two year ago and I know her treatment at times was very limited. Anything that can help or possibly cure this disease is progress!
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By: Cynthia on 9/04/2009 7:20PM
I will talk to my doctors about this new medication. I hope I will be able to get the help that I really need with this medication. Visit www.cynthiafights.com to read my story.
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By: Michelle on 9/01/2009 11:48PM
Wow!I wasn't even sure that there would be many responses, and the little there are, as opposed to what is normally seen on the "gossip/celebrity" related stories. But I am overwhelmed, as a lupus fighter/survivor, and can't even wrap my emotions around this enough to describe what this means to me, both Lynette's story and everyone else's. For those that listed your own stories, thank you as I know I will be looking forward to reading more, I also offer my sincerity, hope, understanding, commraderie, and most of all thoughts and prayers for all of us affected past,present & future. I look forward to hearing more about this new treatment and pray for many more treatments to come out of the shadows and into our light. It's way too overdue! Bless us all.
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By: kj on 9/02/2009 11:06AM
This is great. My mom n law died from it over 10 years and back then they had no idea how to not only treat but, even diagnose it especially in a black woman.
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By: Pat Tetterton on 9/02/2009 1:54AM
I too shall talk to my physician about this new med. I wonder how to get into a trial.
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By: The Missing Link on 9/02/2009 7:18AM
This is very good news, but for far too many very late, I lost my Mom in Nov, 1979 and in a few months it'll be 30 years to Lupus,just reading this story took me back to another time and place you kinda wish time could of frozen.
My prayers are with you all.
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By: dorothy holland on 9/02/2009 12:31PM
The is excellent new. My sister has been suffering with lupus for over 30 years. By the grace of God and her wonderful doctors, she has been able to live a good quality of life. I will share this information with her.
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