Related Experiment Video
Updated: Apr 14, 2026

Determining Immune System Suppression versus CNS Protection for Pharmacological Interventions in Autoimmune Demyelination
Published on: September 12, 2016
The transition from first-line to second-line therapy in multiple sclerosis
1NeuroCure Clinical Research Center and Clinical and Experimental Multiple Sclerosis Research Center, Charité-Universitätsmedizin Berlin, Charitéplatz 1, 10117, Berlin, Germany, jan-markus.doerr@charite.de.
Optimizing multiple sclerosis (MS) treatment involves switching therapies due to inadequate response or tolerability issues. Decisions on transitioning from first-line to second-line therapies should consider individual patient profiles and risk factors for better outcomes.
Area of Science:
- Neurology
- Immunology
- Pharmacology
Background:
- Effective management of multiple sclerosis (MS) activity, especially early on, is vital to prevent long-term disability.
- Current disease-modifying drugs (DMDs) are categorized as first- or second-line, but real-world guidelines for switching therapies are lacking.
- The landscape of MS treatment strategies, including first- and second-line approaches, is continually evolving.
Purpose of the Study:
- To provide evidence-based guidance on optimizing multiple sclerosis (MS) treatment by switching from first-line to second-line therapies.
- To outline decision-making criteria for initiating treatment transitions in MS patients.
- To summarize data supporting treatment optimization based on response, tolerability, safety, and adherence.
Main Methods:
- Review and synthesis of existing data on switching disease-modifying drugs (DMDs) in multiple sclerosis (MS).
- Analysis of reasons for treatment switching, including inadequate response, tolerability, safety concerns, and adherence issues.
- Examination of different therapeutic strategies, such as intra-class switching and escalation to more potent agents.
Main Results:
- Switching from first-line to second-line therapy in MS is motivated by inadequate response, tolerability, safety, or adherence.
- Intra-class switching (e.g., interferon beta to glatiramer acetate) or switching to oral medications (dimethylfumarate, teriflunomide) can be options for tolerability issues.
- Escalation to more potent therapies (natalizumab, fingolimod, alemtuzumab) is suggested for treatment failure, though with potential risk-benefit considerations.
Conclusions:
- Treatment decisions for switching MS therapies must be individualized, considering patient-specific factors and risk profiles.
- While some drugs have varying approval statuses across regions (e.g., fingolimod), direct efficacy comparisons among second-line options are limited.
- A personalized approach is essential for optimizing MS treatment outcomes when transitioning between therapy lines.
Related Concept Videos
Drug Therapy
Antianxiety Medications
Drug Administration and Therapy Phases: Overview
The pharmaceutical phase focuses on leveraging the physicochemical properties of the drug to design and manufacture an effective product. Variants include orally administered tablets or capsules, topical creams or ointments, and parenteral-delivery solutions or emulsions.
The pharmacokinetic phase...
IV Infusion to Oral Dosing: Conversion Methods
Pulmonary Tuberculosis V
Latent tuberculosis infection occurs when TB bacteria are present in a person's body, but are not causing illness or symptoms. It is not contagious, and preventive treatment is crucial to avoid the...
Treatment Resistant Cancers
Treatment Resistent Cancers

