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Published on: February 28, 2021
Diroximel fumarate to treat multiple sclerosis
Y Wang1, P Bhargava2
1Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Diroximel fumarate (DRF), a new oral fumarate treatment for multiple sclerosis, is bioequivalent to dimethyl fumarate (DMF). This review examines DRF's pharmacology, pharmacokinetics, and clinical data, comparing it to the established DMF.
Area of Science:
- Neuroscience
- Pharmacology
- Clinical Therapeutics
Background:
- Multiple sclerosis (MS) is a chronic neurological disease.
- Oral fumarates, such as dimethyl fumarate (DMF), are established treatments for relapsing MS.
- Diroximel fumarate (DRF) is a newer oral fumarate recently approved for relapsing MS.
Purpose of the Study:
- To review the pharmacology, pharmacokinetics, metabolism, clinical studies, and drug safety of diroximel fumarate (DRF).
- To provide a comprehensive overview of DRF as a treatment for relapsing forms of multiple sclerosis.
- To compare DRF with dimethyl fumarate (DMF) based on available data.
Main Methods:
- Literature review of published studies on DRF and DMF.
- Analysis of pharmacological and pharmacokinetic data for DRF.
- Examination of clinical trial data (Phase III) for DRF's safety, tolerability, and efficacy.
Main Results:
- Diroximel fumarate (DRF) is bioequivalent to dimethyl fumarate (DMF), sharing the same active metabolite, monomethyl fumarate.
- DMF has a well-established profile of efficacy, safety, and tolerability.
- DRF has completed one Phase III study, with another ongoing, to further assess its clinical profile.
Conclusions:
- Diroximel fumarate (DRF) represents a new therapeutic option for relapsing multiple sclerosis.
- Understanding DRF's pharmacological and clinical characteristics is crucial for its application in MS treatment.
- Further studies will continue to elucidate the long-term safety and efficacy of DRF compared to DMF.
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