- Mary Elizabeth Dallas
- Posted May 18, 2018
FDA Approves First Drug Aimed at Preventing Migraines
FRIDAY, May 18, 2018 (HealthDay News) -- The millions of Americans who suffer from migraine may have a new source of hope -- the first drug aimed at preventing the headaches gained U.S. Food and Drug Administration approval on Thursday.
Researchers have found that the injected drug, called Aimovig (erenumab), can prevent migraines if other treatments have failed to do so.
"Aimovig provides patients with a novel option for reducing the number of days with migraine," Dr. Eric Bastings, deputy director of the division of neurology products in the FDA's Center for Drug Evaluation and Research, said in an agency news release.
"We need new treatments for this painful and often debilitating condition," he said.
Millions of people suffer from the throbbing pain, light and sound sensitivity, and nausea that can come with migraines.
Aimovig works by blocking a key brain "neurotransmitter" chemical that sends out pain signals, explained a team of researchers who presented their study findings last month at the annual meeting of the American Academy of Neurology (AAN) in Los Angeles.
Working with a group of people with tough-to-treat migraine, the "study found that [Aimovig] reduced the average number of monthly migraine headaches by more than 50 percent for nearly a third of study participants," lead researcher Dr. Uwe Reuter, of The Charite University Medicine Berlin in Germany, said in an AAN news release.
The FDA's approval on Thursday was spurred by the results of studies just like that one.
One study involved 955 people with episodic migraine who were given either Aimovig or a placebo for six months. In that trial, use of the drug was tied to one to two fewer migraine days per month.
In the second study, 577 patients with episodic migraine were given Aimovig or a placebo for three months. Again, those on the drug had at least one less day of headache in a month. Similar results were found in a third, three-month study involving 667 patients -- this time, Aimovig users had 2.5 fewer migraine days per month, the FDA said.
The most common side effects were some injection-site reactions and constipation.
The estimated cost of the drug is $7,000 annually and may be covered by insurance, according to published reports.
One U.S. migraine specialist was enthusiastic about Aimovig's potential.
"We have a new class of drugs -- [Aimovig] likely to be the first to be on the market -- that are showing great promise in preventing migraine attacks," said Dr. Randall Berliner. He's an adjunct neurologist at Lenox Hill Hospital in New York City.
As Berliner explained, it's been a long, tough road to find medicines that provide reliable relief to migraine sufferers.
Twenty years ago, a group of drugs called triptans was introduced, and have since become the standard of care, he said. But they don't work for everyone.
Aimovig, and meds like it, target "calcitonin gene-related peptide" (CGRP). Aimovig acts to stop this neurotransmitting chemical from binding to a nerve and sending out migraine pain signals.
"Our bodies typically produce antibodies to fight off infections, cancers and other foreign agents that the immune system deems harmful. But physicians and scientists have learned to develop antibodies that can target agents that cause disease: tumors, abnormal immune cells, and now CGRP," Berliner explained.
"In so doing, [Aimovig ] very safely blocks a good deal of the migraines from occurring in the first place," Berliner said.
In the study by Reuter and colleagues, which was funded by drug maker Novartis, the investigators tested Aimovig on 246 people with treatment-resistant migraine.
Of these participants, 39 percent had already failed to respond to two available migraine medications, 38 percent were treated with three other medications and 23 percent had tried four different medications to help control their migraines.
On average, these migraine sufferers experienced nine migraine headaches each month and took an acute migraine drug to stop an attack five times each month.
During the study, each person received injections of either 140 milligrams of Aimovig or a "dummy" placebo once per month for three months.
After three months, those treated with Aimovig were almost three times as likely to have fewer days with migraine pain, compared to people who'd only gotten the placebo. Days with migraine headaches were reduced by at least 50 percent compared to those who were given the placebo. In addition to fewer days with headaches, these patients also took acute migraine drugs less often.
Of all the participants, 30 percent treated with Aimovig said their migraine frequency dropped by half. The same was true for only 14 percent in the placebo group. The drug was also not associated with significant side effects.
All of this "can greatly improve a person's quality of life," Reuter said. "Our results show that people who thought their migraines were difficult to prevent may actually have hope of finding pain relief."
What's the next step? According to Reuter, "more research is now needed to understand who is most likely to benefit from this new treatment."
The researchers added that larger studies are also needed to evaluate the long-term safety and effectiveness of the medication.
Dr. Noah Rosen directs the Headache Center at Northwell Health's Neuroscience Institute in Great Neck, N.Y. He agreed that "too many people have suffered because a lack of good migraine-specific prevention and from the side effects of many of the currently available options. If we are able to figure out which migraine sufferers are most likely to benefit from this treatment, it will also let us provide care more effectively."
The American Academy of Family Physicians has more on migraine.
SOURCES: U.S. Food and Drug Administration, news release, May 17, 2018; Randall Berliner, M.D., adjunct neurologist, Lenox Hill Hospital, New York City; Noah Rosen, M.D., director, Headache Center, Northwell Health's Neuroscience Institute, Great Neck, N.Y.; American Academy of Neurology, news release, April 17, 2018
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