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Study identifier: NCT05344469 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A NIS Evaluating Various Injectable and Oral Treatments in Patients With Relapsing Multiple Sclerosis

Condition: Relapsing Multiple Sclerosis  ·  Sponsor: Novartis Pharmaceuticals

PhaseN/A
Planned participants800
Who can joinAll sexes, 18 Years to 100 Years
Healthy volunteersNo

About this study

This is an observational, non-interventional, multicenter, open-label study in patients being treated with any approved injectable or selected oral DMT for RMS in Germany. Prospective, primary data will be collected via questionnaires and an electronic case report form (eCRF) over a period of up to four years. Additionally, medical history of participants will be collected including disease duration, laboratory values, EDSS, MRI parameters and relapses.

This description comes directly from the study's public registry record.

Talk to the study team

Novartis Pharmaceuticals  ·  +41613241111  ·  novartis.email@novartis.com

Novartis Pharmaceuticals

Always discuss trial participation with your own doctor first.

Locations (138)

Novartis Investigative SiteAlbstadt, Baden-Wurttemberg, GermanyRecruiting
Novartis Investigative SiteHettingen, Baden-Wurttemberg, GermanyCompleted
Novartis Investigative SiteHettingen, Baden-Wurttemberg, GermanyRecruiting
Novartis Investigative SiteMannheim, Baden-Wurttemberg, GermanyRecruiting
Novartis Investigative SiteNagold, Baden-Wurttemberg, GermanyRecruiting
Novartis Investigative SiteSchwäbisch Hall, Baden-Wurttemberg, GermanyRecruiting
Novartis Investigative SiteSchwetzingen, Baden-Wurttemberg, GermanyRecruiting
Novartis Investigative SiteBamberg, Bavaria, GermanyActive Not Recruiting
Novartis Investigative SiteDillingen an der Donau, Bavaria, GermanyActive Not Recruiting
Novartis Investigative SiteMunich, Bavaria, GermanyWithdrawn
Novartis Investigative SiteMunich, Bavaria, GermanyWithdrawn
Novartis Investigative SiteNeuburg A.d. Donau, Bavaria, GermanyActive Not Recruiting

+ 126 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05344469