drugset / Trial / NCT03535298

Determining the Effectiveness of earLy Intensive Versus Escalation Approaches for RRMS

NCT03535298

Phase 4 Active not recruiting 800 enrolled The Cleveland Clinic University of Nottingham · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

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.

Timeline

Start
2019-01-03
Primary completion
2027-07-30
Completion
2027-07-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Alemtuzumab Monoclonal antibody
Subject BAF312 Unknown
Subject Cladribine Small molecule
Subject Diroximel fumarate Small molecule
Subject Fingolimod Small molecule
Subject Glatiramer Acetate Small molecule
Subject Interferon-beta Protein / enzyme biologic
Subject Ocrelizumab Monoclonal antibody
Subject Ofatumumab Monoclonal antibody
Subject Ozanimod Small molecule
Subject Ponesimod Small molecule
Subject Rituximab Monoclonal antibody
Subject Teriflunomide Small molecule
Subject Ublituximab Monoclonal antibody
Subject dimethyl fumarate Unknown
Subject monomethyl fumarate Small molecule
Subject natalizumab Monoclonal antibody