Long Term Special Drug Use-results Surveillance for Mayzent in SPMS Patients
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- STATUS
- Recruiting
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- End date
- Feb 28, 2025
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- participants needed
- 330
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- sponsor
- Novartis Pharmaceuticals
Novartis Pharmaceuticals
Primary Contact
Novartis Investigative Site (5.1 mi away) Contact
+167 other locationSummary
This study is a single cohort, central registration system, all-case, open-label, multicenter observational study in patients using Mayzent for the indication of secondary progressive multiple sclerosis.
Description
This is a non-interventional study, and as such there is no binding treatment strategy, diagnosis/treatment procedures or visit schedule. The investigator should administer Mayzent as labelled. Routine medical practice will apply to visit frequency and evaluation variables, and only these data will be collected by the sponsor as part of the study procedures. The investigator should record data in the applicable CRFs at every visit if possible.
Details
| Condition | Secondary Progressive Multiple Sclerosis (SPMS) |
|---|---|
| Treatment | Mayzent |
| Clinical Study Identifier | NCT04593927 |
| Sponsor | Novartis Pharmaceuticals |
| Last Modified on | 5 May 2022 |
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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