Trials / Active Not Recruiting
Active Not RecruitingNCT03535298
Determining the Effectiveness of earLy Intensive Versus Escalation Approaches for RRMS
Determining the Effectiveness of earLy Intensive Versus Escalation Approaches for the Treatment of Relapsing-Remitting Multiple Sclerosis
- Status
- Active Not Recruiting
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 800 (estimated)
- Sponsor
- The Cleveland Clinic · Academic / Other
- Sex
- All
- Age
- 18 Years – 60 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Early Highly Effective Therapies Group | Highly Effective MS Therapy group of medications |
| DRUG | Escalation Therapies Group | Escalation MS Therapy group of medications |
Timeline
- Start date
- 2019-01-03
- Primary completion
- 2027-07-30
- Completion
- 2027-07-30
- First posted
- 2018-05-24
- Last updated
- 2025-08-28
Locations
30 sites across 2 countries: United States, United Kingdom
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT03535298. Inclusion in this directory is not an endorsement.