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-1a Protein / enzyme biologic — —
Subject Interferon beta-1b 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 — —
Subject peginterferon beta-1a Protein / enzyme biologic — —