NEW YORK (Reuters Health)—Romosozumab improves bone mineral density (BMD) in men with osteoporosis, but safety concerns are holding up its approval in the U.S.
“One of the big concerns in the osteoporosis world is the very large osteoporosis treatment gap,” Dr. E. Michael Lewiecki of the New Mexico Clinical Research & Osteoporosis Center, Albuquerque, the study’s first author, tells Reuters Health in a telephone interview. “Unfortunately, most people with osteoporosis who are at high risk for fracture are not currently being treated, and the treatment gap is even worse in men than it is in women.”
Dr. Lewiecki and colleagues wanted to know if the effect of the drug on BMD in men would be similar to its effect in earlier trials in women, i.e., the FRAME study, reported in 2016, and the ARCH trial, reported in 2017.
“If the improvement in bone density with men is similar to what it is in women, then the assumption is that fracture risk is reduced similarly in men as it is in women,” he says.
The 245 men in the study, ages 55–90, all had low baseline BMD and a history of fragility fracture. They were randomly assigned 2:1 to receive 210 mg romosozumab subcutaneously once a month or placebo.
Romosozumab binds sclerostin, increasing bone formation and decreasing resorption.
After 12 months of treatment, lumbar spine BMD had increased by 12.1% in patients on active treatment versus 1.1% for those on placebo. Total hip BMD increased 2.5% with romosozumab and declined 0.5% with placebo.
Although adverse events and serious adverse events were similar with romosozumab and placebo, there were eight positively adjudicated cardiovascular serious adverse events in patients on romosozumab (4.9%) vs. two in the placebo group (2.5%).
In 2017, the U.S. Food and Drug Administration rejected Amgen’s application to approve romosozumab, after safety data suggested a link between the drug and cardiovascular adverse events.
The original FRAME study, which compared romosozumab to placebo, had been free of cardiovascular concerns but missed its secondary endpoint of nonvertebral fractures. In the ARCH trial, serious cardiovascular adverse events were observed more often with romosozumab than with alendronate.
“Amgen is carefully analyzing all of the clinical trial data and will submit a letter of response to the FDA sometime this summer, and then the FDA will respond to that and we’ll see what happens,” Dr. Lewiecki says. “It’s too early to speculate on whether it’s going to be approved or exactly what the indications for the treatment will be.”