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2023-506863-32-00CompletedPhase 1

A Study to Investigate the Safety, Tolerability, Immunogenicity, Pharmacokinetics, and Pharmacodynamics of Ascending Intravenous Doses of Glofitamab, Administered after Ocrelizumab Pretreatment, in Patients with Multiple Sclerosis

Source: EU CTIS (euclinicaltrials.eu) · Last updated 3 Sept 2025

Next steps

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
5 (actual)
First submitted
11 Jun 2024
Start date
25 Jul 2023
Lead sponsor
F. Hoffmann-La Roche AG
EU CT number
2023-506863-32-00
EudraCT number
2022-001209-33

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 5
  • 3 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Sites (3)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Fakultni Nemocnice Hradec KraloveNovy Hradec KraloveCzechiaCompleted
KBC ZagrebGrad ZagrebCroatiaCompleted
Klinicki bolnicki centar Sestre milosrdniceGrad ZagrebCroatiaCompleted

Are you the coordinator? Confirm the details

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