๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2025-08-22

Determining the Effectiveness of earLy Intensive Versus Escalation Approaches for RRMS (NCT03535298)

Determining the Effectiveness of earLy Intensive Versus Escalation Approaches for the Treatment of Relapsing-Remitting Multiple Sclerosis

๐Ÿ”ต Active, Not Recruiting Phase4 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: The Cleveland Clinic

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

The DELIVER-MS study seeks to answer the question: Does early treatment with highly effective DMT improve the prognosis for people with MS? This is an area of significant controversy and no data currently exist to guide treatment choices for patients and clinicians. The study results will help guide overall treatment philosophy and will be applicable not only to a wide range of existing therapies but also to new therapies, meeting a significant unmet need in patient decision making and aiding the decision for medication approval by third parties.

Who can join: Review the eligibility criteria below.

Location: University of Colorado-Anschutz Medical Campus โ€” Aurora, Colorado

Age range: 18 Years to 60 Years

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (30 Sites)

Showing the first 25 of 30 sites.

  • University of Colorado-Anschutz Medical Campus โ€” Aurora, Colorado
  • University of Minnesota โ€” Minneapolis, Minnesota
  • Mayo Clinic โ€” Rochester, Minnesota
  • Cleveland Clinic Lou Ruvo Center for Brain Health โ€” Las Vegas, Nevada
  • University of Buffalo โ€” Buffalo, New York
  • University Rochester Medical Center โ€” Rochester, New York
  • University of Cincinnati โ€” Cincinnati, Ohio
  • Cleveland Clinic โ€” Cleveland, Ohio
  • Ohio Health โ€” Columbus, Ohio
  • UT-Austin โ€” Austin, Texas
  • Baylor College of Medicine, Houston โ€” Houston, Texas
  • UTHealth-Houston โ€” Houston, Texas
  • University of Virginia โ€” Charlottesville, Virginia
  • Virginia Commonwealth University โ€” Richmond, Virginia
  • University of Wisconsin-Madison โ€” Madison, Wisconsin
  • University Hospitals Coventry and Warwickshire โ€” Coventry, England
  • The Leeds Teaching Hospitals NHS Trust, Leeds General Infirmary โ€” Leeds, England
  • University Hospitals Leicester โ€” Leicester, England
  • Imperial College Healthcare NHS Trust, Charing Cross Hospital โ€” London, England
  • University College London Hospitals NHS Foundation Trust, University College Hospital โ€” London, England
  • Salford Royal NHS Foundation Trust, Salford Hospital โ€” Manchester, England
  • Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital โ€” Oxford, England
  • University Hospitals Plymouth NHS Trust, Derriford Hospital โ€” Plymouth, England
  • Sheffield Teaching Hospitals โ€” Sheffield, England
  • University Hospitals of North Midlands โ€” Stoke, England

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Review the official NIH record below to find the coordinating site.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—