An update on combination therapies for multiple sclerosis: where are we now?

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Introduction
In theory, combination of two agents, which are suboptimal when given individually, may result in a significant increase in therapeutic effect. Combination therapies have proven particularly effective against infections such as HIV, cancer, and also chronic autoimmune diseases such as rheumatoid arthritis.

Areas covered
The authors review the literature, searching for randomized placebo-controlled or comparative, double-blind or investigator-blinded clinical trials, not including open label clinical trials, of treatment of multiple sclerosis (MS) with combination therapy or add-on therapy, including trials of induction therapy, trials for prevention of disease activity or worsening, amelioration of adverse effects, and treatment of relapses, and trials to increase remyelination.

Expert opinion
Combination of two platform therapies (Interferon-beta or glatiramer acetate) was without additional effect. Clinical trials with add-on, often applying repurposed drugs (e.g. simvastatin, atorvastatin, minocycline, estriol, cyclophosphamide, azathioprine, albuterol, vitamin D), have been negative, apart from monthly methylprednisolone that, however, had low tolerability. Combination therapy for neuroprotection/remyelination showed some interesting results, though we are still awaiting results of phase III trials. The results of combination of anti-inflammatory therapies have in general been disappointing. In the future, combination of new effective neuroprotective/remyelinating drugs and highly effective anti-inflammatory treatments may benefit people with MS.

KEYWORDS: (5-8) Multiple sclerosisdisease-modifying therapycombination therapyadd-on therapytreatment of disease activitytreatment of relapsesneuroprotective therapyremyelinating therapy
OriginalsprogEngelsk
TidsskriftExpert Review of Neurotherapeutics
Vol/bind23
Udgave nummer12
Sider (fra-til)1173-1187
Antal sider15
ISSN1473-7175
DOI
StatusUdgivet - 2023

ID: 387696134