Skip to main content
NIH Record - National Institutes of Health

New MS Treatment Trial Compares Stem Cell Transplant to Best Available Drugs

A clinical trial has begun testing an experimental stem cell treatment against the best available biologic therapies for severe forms of relapsing multiple sclerosis (MS). The trial, sponsored by NIAID, will compare the safety, efficacy and cost-effectiveness of the two approaches.

MS is an autoimmune disease in which a person’s own immune cells attack the central nervous system. The experimental treatment involves using a mixture of four chemical agents to remove these immune cells. Some of the person’s own blood-forming stem cells, which were extracted before treatment, are then infused back into the individual. These cells repopulate the immune system, allowing it to reset itself so that the new immune cells no longer attack the central nervous system. This form of treatment is called autologous hematopoietic stem cell transplantation, or AHSCT. 

“For many people with MS—a chronic, debilitating, unpredictable and currently incurable disease—daily life can be a challenge,” said NIAID director Dr. Anthony Fauci. “AHSCT has the potential to halt the progress of relapsing MS, eliminate the need for a person to take lifelong medication and allow the body to partially regain function. However, we need to be certain that the benefits of this form of treatment outweigh its serious risks.”  

It is estimated that MS affects more than 2.3 million people worldwide, mostly women, including more than 1 million people in the United States. Symptoms of the disease vary widely and may include motor and speech difficulties, weakness, fatigue and chronic pain. The most common form of the disease is relapsing-remitting MS, which is characterized by periods of mild or no symptoms interspersed with symptom flare-ups, or relapses. Incomplete recovery from relapses often leads to increasing disability. Over years, the disease can worsen and shift to a progressive form that may also include relapses. 

The Food and Drug Administration has approved more than a dozen drugs for the treatment of relapsing forms of MS. These drugs vary in efficacy, safety and cost. For many people with severe forms of relapsing MS, first- and second-line drugs fail to adequately control the disease. Previous studies have suggested that AHSCT may be an effective and durable treatment for these individuals. But it has never been formally compared head-to-head with the available third-line drugs, which are highly effective but can have harsh side effects. AHSCT also carries the risks of serious side effects, and even death.

Given these risks and benefits, investigators aim to determine whether AHSCT is an appropriate treatment option for people with severe forms of relapsing MS who would otherwise receive one of the best available third-line biologic drugs. 

The NIH Record

The NIH Record, founded in 1949, is the biweekly newsletter for employees of the National Institutes of Health.

Published 25 times each year, it comes out on payday Fridays.

Associate Editor: Carla Garnett
Carla.Garnett@nih.gov

Staff Writers:

Eric Bock
Eric.Bock@nih.gov

Dana Talesnik
Dana.Talesnik@nih.gov

Back to Top