New phase 3, randomized, double-blind clinical trial was conducted to know the safety and efficacy of teriflunomide, an oral immunomodulatory drug approved for the treatment of adults with relapsing multiple sclerosis.
Teriflunomide was recently approved by the European Commission for children aged 10–17 years with a diagnosis of relapsing remitting multiple sclerosis, based on the trial’s results in Lancet Neurology Multiple sclerosis is a condition in which the immune system attacks the protective covering of nerves in the brain and spinal cord—and most therapies for the disease have not been tested in children.
‘New phase 3 clinical trial results did not show a slowdown of relapses of multiple sclerosis with teriflunomide, which could be due to the study design.’
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In TERIKIDS, 109 children were randomized to receive teriflunomide and 57 were randomized to receive placebo for up to 96 weeks.Read More..
Open-label extension phase entry was possible before the end of the double-blind period for patients who experienced a relapse or demonstrated high disease activity on MRI imaging tests.
More patients in the placebo group entered the open-label extension phase than anticipated, with 26% of patients switching from placebo to teriflunomide before 96 weeks.
After 96 weeks, there was no difference in time to first clinical relapse of multiple sclerosis with teriflunomide compared with placebo.
Teriflunomide was well tolerated—serious adverse events occurred in 11% of patients in the teriflunomide group and 11% of patients in the placebo group.
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“The trial did not meet its primary endpoint—delaying time to the next clinical relapse—possibly because of more frequent switches to the open-label arm due to high MRI activity.
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Chitnis notes that an ongoing open-label treatment extension study is continuing to evaluate the long-term effects of teriflunomide in young patients.
Source-Medindia