Trials / Completed
CompletedNCT00472797
Rebif New Formulation (RNF) Quality of Life (QOL) Study
A Randomized, Multicenter, Two-arm, 12 Week Phase IIIb Study to Evaluate Quality of Life (QOL) Measures in Subjects With Relapsing Forms of Multiple Sclerosis (MS) Who Are Transitioning From Rebif® (Interferon Beta-1a) to Rebif New Formulation (RNF)
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 232 (actual)
- Sponsor
- EMD Serono · Industry
- Sex
- All
- Age
- 18 Years – 60 Years
- Healthy volunteers
- Not accepted
Summary
To evaluate the impact on Quality of Life (QOL), tolerability, treatment satisfaction, and injection site redness Rebif treated subjects with relapsing forms of MS who transition to a new formulation of Rebif (RNF).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Rebif New Formulation Non Titrated | human interferon beta 1a - Rebif New Formulation |
| DRUG | Rebif New Formulation Titrated | Human interferon beta 1a Rebif New Formulation |
Timeline
- Start date
- 2007-04-01
- Primary completion
- 2009-02-01
- Completion
- 2009-11-01
- First posted
- 2007-05-14
- Last updated
- 2013-08-07
- Results posted
- 2009-09-02
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00472797. Inclusion in this directory is not an endorsement.