A Study to Investigate Effects of Ocrelizumab Treatment on Neurofilament Light Chain (NfL)
The main purpose of the study is to evaluate participant satisfaction after administration of ocrelizumab subcutaneous (SC) after 12 months using the therapy administration satisfaction questionnaire subcutaneous (TASQ-SC).
| Condition(s) | Multiple Sclerosis |
|---|---|
| Status | Recruiting |
| Study type | Observational |
| Summary | The main purpose of the study is to evaluate participant satisfaction after administration of ocrelizumab subcutaneous (SC) after 12 months using the therapy administration satisfaction questionnaire subcutaneous (TASQ-SC). |
| Who can participate | Inclusion Criteria: * Diagnosis of MS * RMS and PPMS participants diagnosed according to the McDonald criteria of 2017 * First treatment during the course of MS therapy with ocrelizumab SC according to the local prescribing information, regardless of the reason for starting treatment with ocrelizumab Exclusion Criteria: * Participation in interventional studies investigating DMTs for MS * Prior or simultaneous participation in CONFIDENCE or MoOzaRt (ISRCTN55332718) non interventional study (NIS) at the same study site * Prior treatment with rituximab (MabThera®) or ublituximab (Briumvi®) * Severe psychiatric disability * Pregnant women |
| Ages | 18 Years |
| Sex | All |
| Lead sponsor | Hoffmann-La Roche |
| Locations | Aachen, Germany; Amberg, Germany; Arnsdorf, Germany; Aschaffenburg, Germany; Bad Soden, Germany; Bamberg, Germany (+84 more sites) |
| Start date | 2024-09-26 |
| NCT ID | NCT06780150 |
| Official listing | https://clinicaltrials.gov/study/NCT06780150 |