Abstract
There are currently six disease-modifying drugs approved for relapsing forms of multiple sclerosis. Their efficacy has been proven in multiple clinical trials. The four therapies licensed as first-line agents (three formulations of interferon-beta and one of glatiramer acetate) have well-established short-term and long-term safety profiles, with manageable adverse events. Results of recent trials suggest that current disease-modifying drugs may have better on-treatment disease suppression than was predicted by the results of the original pivotal studies. Although these therapies are all parenterally administered, a number of technological advances have improved various aspects of injection tolerability and enhanced acceptability, so that the impact of self-injection on the patient's life is minimized. Several promising oral disease-modifying drugs are now in phase III development. However, as these drugs are new to multiple sclerosis therapy, their short-term and long-term safety profiles are unknown. Although novel therapies for multiple sclerosis, particularly orally administered drugs, are eagerly awaited, they will not immediately replace the tried and trusted options.
| Original language | English |
|---|---|
| Pages (from-to) | S4-S9 |
| Journal | Current Opinion in Neurology |
| Volume | 22 |
| Issue number | SUPPL. 1 |
| DOIs | |
| State | Published - Mar 2009 |
Keywords
- Disease-modifying drug
- Glatiramer acetate
- Interferon-beta
- Multiple sclerosis
- Parenteral therapy
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