Study Description
Study to evaluate the effectiveness of ofatumumab in Italian RRMS patients in the
real-life setting. Prospective real-world data on ofatumumab is still very limited. For this reason, the
main aim of this study is to investigate the impact of ofatumumab in a population of
Italian RRMS patients in routine clinical practice to evaluate if ofatumumab is able in
these conditions to provide relevant clinical benefits that comprehensively encompass
anti-inflammatory activity (relapses), disability accumulation, cognitive impairment,
fatigue symptoms and quality of life.
This is an observational, multicenter, single-arm, prospective study. Prospective data
will be collected on patients newly treated with ofatumumab over an observational period
of 12 months.
Interventions
Ofatumumab
Eligibility Criteria
Inclusion Criteria:
1. Male or female outpatients ≥18 years old.
2. Patients diagnosed with RRMS (McDonald criteria 2017).
3. Patients newly treated with ofatumumab, for whom the decision to start treatment
with the drug has already been taken independently from study inclusion, based on
clinical practice and according to the SmPC and to AIFA reimbursement criteria and
who already successfully qualified for treatment with ofatumumab (i.e., passed the
screening procedure mandated by the SmPC and the Risk Management Plan (RMP) for this
treatment).
4. Patient or a legal representative of the patient must provide written informed
consent before any study assessment is performed.
Exclusion Criteria:
1. Patients outside the approved label of ofatumumab.
2. Pregnant and lactating women.
3. Patients with any clinical condition that may interfere with the subject's ability
to cooperate and comply with the study procedures based on investigator's judgement.
4. Patients cannot participate in this non-interventional study if they also
participate in an interventional trial.
5. Treatment with ofatumumab prior to inclusion in this study or after 7 days from
baseline visit.
Novartis Investigative Site
Recruiting
Roma,RM,00189,Italy
Novartis Investigative Site
Recruiting
Pozzilli,IS,86077,Italy
Novartis Investigative Site
Recruiting
Sassari,SS,07100,Italy
Novartis Investigative Site
Recruiting
Monza,MB,20900,Italy
Novartis Investigative Site
Recruiting
Trento,TN,38100,Italy
Novartis Investigative Site
Recruiting
Palermo,PA,90127,Italy
Novartis Investigative Site
Recruiting
Ancona,AN,60126,Italy
Novartis Investigative Site
Recruiting
Gallarate,VA,21013,Italy
Novartis Investigative Site
Recruiting
Pavia,PV,27100,Italy
Novartis Investigative Site
Recruiting
Cona,FE,44100,Italy
Novartis Investigative Site
Recruiting
Napoli,80131,Italy
Novartis Investigative Site
Recruiting
Ravenna,RA,48100,Italy
Novartis Investigative Site
Recruiting
Foggia,FG,71122,Italy
Novartis Investigative Site
Recruiting
Roma,RM,00168,Italy
Novartis Investigative Site
Recruiting
Firenze,FI,50134,Italy
Worldwide Contacts
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