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Participate in a Clinical Trial

Without the participation of people with MS, it would be impossible to develop new and better therapies and other interventions.

Clinical Trials in MS


The latest clinical research in MS, including trials funded by the Society and trials in progressive MS.

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Posting a Trial

If you would like us to post a study on these pages, please email studies@nmss.org to find out what information you need to submit for review.

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Clinical trials help to determine if treatments are safe and effective. Studies are monitored to ensure that the rights and safety of all participants are protected. Make an informed decision before agreeing to participate. Read more in our Guide to Participating in Clinical Trials.

Clinical Trials In Your Area

Interested in clinical trials? Simply search by state, type of MS or keyword and see what’s going on in your area.

  1. Clinical Trial: Arbaclofen extended release tablets

    Researchers are recruiting men with MS and spasticity to determine the effects of Arbaclofen extended release tablets on sperm.
  2. Clinical Trial: ALKS 8700 vs. Dimethyl Fumarate

    Investigators are recruiting 420 people with relapsing-remitting MS for a phase 3 study comparing gastrointestinal side effects experienced during treatment with oral ALKS 8700 (Alkermes, Inc.) or Tecfidera ®  (dimethyl fumarate, Biogen, Inc.). The study is funded by Alkerm...
  3. Clinical Trial: ALKS 8700

    This study will evaluate the long-term safety and tolerability of oral ALKS 8700 for the treatment of RRMS
  4. Clinical Trial: ALKS 8700

    A phase 3 open label study to evaluate the long term safety and tolerability of ALKS-8700 in adults with Relapsing and Remitting Multiple Sclerosis.
  5. Clinical Trial: Spasticity Management Program

    Participants will be placed randomly into one of two groups and will receive one of two different spasticity management programs. Each program consists of education and exercise training intended to help reduce spasticity. All participants will attend two 2-hour group se...

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