Wednesday, 12 February 2014

New Drug Shows Promise for Restless Legs Syndrome: Study

WEDNESDAY Feb. 12, 2014, 2014 -- For relieving symptoms of restless legs syndrome and slowing its progression, the drug pregabalin (Lyrica) outperformed the current standard medication in a head-to-head comparison, a new study found.
Pramipexole (Mirapex), which is commonly used to treat this neurological disease, makes many people worse, said lead researcher Richard Allen, an associate professor of neurology at Johns Hopkins University School of Medicine in Baltimore.
Lyrica works just as well and doesn't worsen the condition, Allen said.
People with restless legs syndrome -- now also known as Willis-Ekbom disease -- feel throbbing, creeping or other unpleasant sensations in the legs and an uncontrollable urge to move them.
Symptoms occur primarily at night, and most people with restless legs syndrome have trouble falling asleep and staying asleep. Moving the legs relieves the discomfort; remaining in a resting position often activates symptoms. Untreated, the condition results in exhaustion and daytime fatigue, experts say.
"When the disease becomes worse it can become really bad," Allen said. Besides disturbing sleep, it affects patients 24 hours a day, he noted.
The report, published Feb. 13 in the New England Journal of Medicine, was funded by Pfizer, the maker of Lyrica.
"Long-term management of restless legs syndrome affecting sleep and quality of life remains problematic," said Dr. Sudhansu Chokroverty, from the New Jersey Neuroscience Institute at JFK Medical Center in Edison. Chokroverty wrote an accompanying journal editorial.
The most commonly used medications, called "dopamine agonists," are associated with worsening of the disease in a large number of patients, he said.
This multicenter study was launched in an attempt to resolve "the vexing problem of long-term issues in restless legs syndrome," Chokroverty said.
Although Allen thinks Lyrica should be seen as a viable treatment for restless legs syndrome based on the current findings, Chokroverty said further studies are still needed. Whether Lyrica's positive effects will be sustained without undesirable side effects and whether the treatment will improve quality of life, including sleep, are among the questions that need to be addressed, he said.
"Many gaps remain in our knowledge about treatment of restless legs syndrome," Chokroverty said. "Hopefully, this recent progress in research will encourage researchers to develop an ideal drug for this common but uncommonly diagnosed condition."
Allen noted that Lyrica is expensive, running to more than $250 for 60 capsules. But there are less expensive alternatives, such as generic gabapentin, which can cost less than $14 for 90 capsules, he said.
For the trial, Allen's team randomly assigned about 720 patients with moderate to severe symptoms of restless legs syndrome to Lyrica versus Mirapex, or Mirapex versus an inactive placebo.
Over 12 weeks of treatment, patients taking Lyrica showed greater improvement in symptoms, compared with those taking placebo (about 71 percent versus 47 percent), the researchers found.
Moreover, over 40 or 52 weeks of treatment, significantly fewer patients taking Lyrica saw their condition worsen compared to those taking Mirapex (2 percent versus nearly 8 percent), the authors noted.
That finding suggests that worsening of the condition is caused by dopamine agonists, not a natural occurrence, the study authors pointed out.
"Restless legs syndrome is a progressive disease. The question is not do people get worse over time -- they do," Allen said. "But dopamine [agonists] make patients worse than they were before. We get people who have symptoms 24 hours a day, which is profoundly disturbing."
In terms of side effects, six of the patients taking Lyrica had suicidal thoughts, as did five taking Mirapex.
More information
For more information on restless legs syndrome, visit the U.S. National Institute of Neurological Disorders and Stroke.

FDA Approves Imbruvica to Treat Chronic Lymphocytic Leukemia

February 12, 2014 -- The U.S. Food and Drug Administration today expanded the approved use of Imbruvica (ibrutinib) for chronic lymphocytic leukemia (CLL) patients who have received at least one previous therapy.
CLL is a rare blood and bone marrow disease that usually gets worse slowly over time, causing a gradual increase in white blood cells called B lymphocytes, or B cells. The National Cancer Institute estimates that 15,680 Americans were diagnosed and 4,580 died from the disease in 2013.
Imbruvica works by blocking the enzyme that allows cancer cells to grow and divide. In November 2013, the FDA granted Imbruvica accelerated approval to treat patients with mantle cell lymphoma, a rare and aggressive type of blood cancer, if those patients received at least one prior therapy.
“Today’s approval provides an important new treatment option for CLL patients whose cancer has progressed despite having undergone previous therapy,” said Richard Pazdur, M.D., director of the Office of Hematology and Oncology Products in the FDA’s Center for Drug Evaluation and Research. “The FDA completed its review of Imbruvica’s new indication under the agency’s accelerated approval process, which played a vital role in rapidly making this new therapy available to those who need it most.”
Under the agency’s accelerated approval process, the FDA may approve a drug based on a surrogate or intermediate endpoint that is reasonably likely to predict clinical benefit. Drugs receiving accelerated approval are usually subject to an agreement to conduct confirmatory trials verifying and describing clinical benefit. Imbruvica for CLL also received priority review and orphan-product designation because the drug demonstrated the potential to be a significant improvement in safety or effectiveness in the treatment of a serious condition and is intended to treat a rare disease, respectively.
The FDA’s accelerated approval of Imbruvica for CLL is based on a clinical study of 48 previously treated participants. On average, participants were diagnosed with CLL 6.7 years prior to the study and had received four previous therapies. All study participants received a 420 milligram orally administered dose of Imbruvica until the treatment reached unacceptable toxicity or the disease progressed. Results showed nearly 58 percent of participants had their cancer shrink after treatment (overall response rate). At the time of the study, the duration of response ranged from 5.6 to 24.2 months. An improvement in survival or disease-related symptoms has not been established.
The most common side effects observed in the clinical study include low levels of platelets in the blood (thrombocytopenia), diarrhea, bruising, a decrease in infection-fighting white blood cells (neutropenia), low red blood cells (anemia), upper respiratory tract infection, fatigue, pain in the muscles and bones (musculoskeletal pain), rash, fever (pyrexia), constipation, swelling of tissues (peripheral edema), joint pain (arthralgia), nausea, mouth sores (stomatitis), sinus infection (sinusitis) and dizziness.
Imbruvica is manufactured by Sunnyvale, Calif.-based Pharmacyclics.
Source: FDA
Posted: February 2014