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NCT07168694Completed

A Real-world Study About the Impact of Siponimod Treatment on Secondary Progressive Multiple Sclerosis Patients in Russia

Retrospective, Multicenter, Non-interventional (Observational) Study With the Aim to Describe the Impact of Siponimod Treatment in a Real-world SPMS Population in Russia

Source: ClinicalTrials.gov · Last updated 11 Sept 2025

Brief summary (registry, in English)

The main aim of the study was to describe the demographic and clinical characteristics of patients with secondary progressive multiple sclerosis (SPMS) who were receiving siponimod therapy in Russia. This study analyzed data from outpatient records/medical records collected across 11 Russian multiple sclerosis (MS) centers. Data collection was carried out from April 16, 2024 to September 26, 2024.

Status (registry)
Completed
Study type
Observational
Enrollment
606 (actual)
First submitted
4 Sept 2025
Start date
16 Apr 2024
Primary completion date
26 Sept 2024
Lead sponsor
Novartis Pharmaceuticals
NCT number
NCT07168694

What you commit to

  • Study type: Observational
  • Participants enrolled: 606
  • From 16 Apr 2024 to the primary completion date, 26 Sept 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • None.

Who the study is looking for

  • Documented diagnosis of SPMS, with or without relapses.
  • Treatment with siponimod for at least 6 months.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Novartis
Coordinator of this site? Confirm its status
East HanoverUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.