It has been found that a commonly-prescribed multiple sclerosis (MS) infusion medication, linked to a rare but serious side effect, is safer to use when dosing intervals are extended.

According to a new study led by MS specialists NYU Langone Health, changing the dosing from 4 weeks to 5-12 weeks reduces the risk for Progressive Multifocal Leukoencephalopathy (PML). PML is a rare but potentially fatal brain infection. The findings could influence how neurologists prescribe the medication. "Neurologists have been looking for safer ways to administer natalizumab infusions to their patients, but there hasn't been clear data on whether decreasing dosing frequency improves safety", said first author Lana Zhovtis Ryerson.

Lana continued, "Our safety findings are clinically and statistically significant, and we believe that extending the dosing schedule of natalizumab is practice changing and may save lives". Natalizumab, a monoclonal antibody, is used to prevent MS relapses, improve quality of life, and slow worsening disability. The medication is indicated to be prescribed in 300-milligram infusion doses every 4 weeks. Taking the medication longer than two years, however, may increase risk PML, which is caused by the John Cunningham virus (JCV).

There have been 756 PML cases reported worldwide as of January 2018, with a global incidence rate of 4.19 per 1,000 PML cases in people treated with natalizumab. Patients who test JCV antibody-positive are typically either told to not to start natalizumab, or have had treatment stopped after two years when risk was deemed to be too high. The new study, however, reported safety data through up to 6 years, when the extended dosing regimens were applied, with risk reduction for PML as high as 94 percent.

Researchers reviewed data on all patients who have been exposed to JCV who are enrolled in TOUCH, the U.S. Food and Drug Administration-mandated Risk Evaluation and Mitigation Strategy (REMS) program for natalizumab that requires manufacturers to document all uses of a medication to ensure that the benefits of a drug outweigh its risks. Since the optimal extended dose schedule is not known, researchers chose to look at the data in multiple ways – with the primary definition looking at extended dose history in the last 18 months, the secondary definition looking at extended dose occurring at any time in the dosing history, and for tertiary definition looking primarily at how extended dose history affects PML risk.

The results showed clinically and statistically significant risk reductions with all definitions. The new study did not look at drug efficacy comparing extended to standard doses. However, previous research led by Dr Zhovtis-Ryerson's group found extending the dose up to 8 weeks did not negatively affect the medication's efficacy in a retrospective sample of 2,000 people.

The authors are planning prospective efficacy studies of extended dose natalizumab. The study was presented at the Americas Committee for Treatment and Research in Multiple Sclerosis (ACTRIMS) Forum 2018 in San Diego.