This quiz is for registered users only.



These are monthly webinar presentations for the TREAT-MS clinical trial. Clinical site coordinators and investigators are encouraged to attend the live sessions on the 1st Wednesday at 3:00 pm EST or Thursday at 9:00 am EST of each month. The webinar slides and video recordings are posted here within a few days of the live session. 

March 2018 Webinar 1 PDF slides Main Feature: JHM Single IRB Review Process presented by Megan Singleton and Cindy MacInnis
April 2018 Webinar 2 PDF slides Main Feature: 90-day Start Up Overview presented by Karen Lane
May 2018 Webinar 3 PDF slides Main Feature: Protocol Training presented by Ellen Mowry and Scott Newsome
June 2018 Webinar 4 PDF slides Main Feature: Training of Live Database (Live Demo) presented by Steve Mayo 
July 2018 Webinar 5 PDF slides Main Feature: Tips for Success presented by Madiha Qutab, Ellen Mowry, Scott Newsome and Blake Dewey
August 2018 Webinar 6 PDF slides Main Feature: Patient Retention presented by Ellen Mowry and Scott Newsome
September 2018 Webinar 7  PDF slides Main Feature: MRI in the TREAT-MS Study presented by Blake Dewey
October 2018 Webinar 8 PDF slides Main Feature: Clarifications for Case Report forms presented by Scott Newsome, Ellen Mowry, and Madiha Qutab
November 2018 Webinar 9 PDF slides Main Features: The Rowing Competition in Depth presented by Christina Grabarits and Strategies and Tips for Enrollment Success presented by Dr. Tiri Gyang, Victoria Hope and Dr. Dennis Dietrich
December 2018 Webinar 10 PDF slides Main Feature: TREAT-MS EDC Walkthrough: Live Demo by Steve Mayo


The TREAT-MS Clinical Trial for Multiple Sclerosis (MS) Patients

There is an unmet need to identify if specific treatment strategies during the relapsing-remitting phase of multiple sclerosis (MS) can prevent, delay, or reduce longer-term disability. Currently, there is a lack of evidence-based guidelines to help clinicians and patients determine which treatment strategy is best for an individual with MS. In addition, it is unclear when people with MS, in the setting of breakthrough disease activity, should switch therapies and whether to consider a different first-line therapy or if they should escalate immediately to higher-efficacy therapies.

The TRaditional versus Early Aggressive Therapy for Multiple Sclerosis (TREAT-MS) Trial will help inform patients and the broader healthcare community on whether patients would most benefit from early, possibly more risky aggressive therapy or if starting with a less aggressive (and, often, less risky) therapy, followed by a switch if breakthrough disease activity occurs, is warranted. In addition, this study will help identify if there is a specific patient population or short-term biomarker(s) that is strongly predictive of long-term disability that can result from MS.

The TREAT-MS Trial is a randomized controlled trial that will recruit 900 patients across approximately 45 sites within the United States. In order to be eligible, participants must have relapsing-remitting MS and be between the ages of 18 and 60 years. Participants will need to be eligible for at least one of the higher-efficacy therapies based on screening labs. Participants are not eligible if they have had more than 6 months’ exposure to one or more MS disease-modifying therapies or prior treatment with rituximab, ocrelizumab, alemtuzumab, mitoxantrone, cladribine, or an experimental aggressive therapy.

Participants that meet the eligibility criteria will initially be divided into two groups based on suspected risk(s) for long-term disability. The first group will include those with “high-risk” indicators for aggressive disease versus “low-risk.” Within each group, eligible participants will be randomized 1:1, to either a “higher-efficacy” therapy (i.e., infusible therapies) versus traditional, first-line therapy (injectable and oral therapies). Participants and their neurology specialist will choose the therapy within the category that participants are randomized to that is most appropriate for them. Those deemed at low risk for disability who are initially randomized to a traditional therapy and who experience breakthrough disease activity will be re-randomized to a higher-efficacy therapy or to a different traditional therapy. An extremely important goal for any intervention is to help improve or maintain a high quality of life; therefore, in addition to classic clinical endpoints (i.e., slowing disability progression), patient-reported outcomes will be obtained in order to gain a better understanding of the full impact of a treatment. Study participation will range from 42 – 54 months, depending on enrollment date and study related activities will occur around a participant’s standard of care visits.

For more information on the TREAT-MS trial, please email the team at Johns Hopkins at This email address is being protected from spambots. You need JavaScript enabled to view it. and we will connect you with a participating site in your area.

Principal Investigators: Ellen M. Mowry, MD, MCR & Scott D. Newsome, DO

Sponsor: Johns Hopkins University School of Medicine

Application No: IRB00143534 


To know more about Multiple Sclerosis:

Here are the documents for TREAT-MS.