ITAKOS - Italian Observation, Multicenter, Prospective Study of Ofatumumab in RRMS Patients

NCT06345157 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 379

Last updated 2026-04-13

No results posted yet for this study

Summary

Study to evaluate the effectiveness of ofatumumab in Italian RRMS patients in the real-life setting.

Conditions

  • Multiple Sclerosis, Relapsing-Remitting

Interventions

DRUG

Ofatumumab

This is an observational study. There is no treatment allocation. The decision to initiate treatment with ofatumumab (Kesimpta®) will be based solely on clinical judgement and according to the SmPC and AIFA reimbursement criteria.

Sponsors & Collaborators

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-07-30
Primary Completion
2026-06-30
Completion
2026-06-30

Countries

  • Italy

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06345157 on ClinicalTrials.gov