 Last Update: Jul 07, 2026 

 Ofatumumab in Portuguese Multiple Sclerosis Patients - an Observational Study 

ClinicalTrials.gov Identifier: [NCT05809986](https://clinicaltrials.gov/ct2/show/NCT05809986)

 

Novartis Reference Number:COMB157GPT04

 

 [See if you Pre-qualify](#trial-eligibility "See if you Pre-qualify") 

 All compounds are either investigational or being studied for (a) new use(s). Efficacy and safety have not been established. There is no guarantee that they will become commercially available for the use(s) under investigation. 

 

##  Study Description 

This non-interventional study will compare the effect of Ofatumumab treatment between patients that began Ofatumumab within the 3 years after Multiple Sclerosis diagnosis and patients that began Ofatumumab with more than 3 years of Multiple Sclerosis diagnosis in a real-world setting in Portugal. This is a 2 cohort, multi-center, observational study carried out in Portugal that aims to describe the effectiveness of Ofatumumab in a setting of routine medical care. Primary data will be collected from Multiple Sclerosis patients who initiate Ofatumumab early and later in their disease (cohorts 1 and 2, respectively).

Data will be collected during 3 visits distributed over a maximum period of 24 months. Exceptionally, if the patient shows Expanded Disability Status Scale (EDSS) worsening in visit 2 or 3 (12 and 24 months after Ofatumumab initiation, respectively), there will be an additional visit 6±1 months after visit 2 or 3 for EDSS confirmation.

The study includes patients that have initiated Ofatumumab up to 12 months prior inclusion in the study OR Patients that are initiating Ofatumumab at the moment of study inclusion.

Patients in both cohorts will have to be treated with Ofatumumab for at least two years to compare No Evidence of Disease Activity (NEDA)-3 at 12 to 24 months, respectively.



 

 Condition Relapsing Multiple Sclerosis 

 

 Overall Status Recruiting 

 

 Number of Participants174

 

 

 Start Date Nov 27, 2023 

 

 Completion Date Dec 31, 2026 

 

 Gender All 

 

 Age(s) 18 Years - 99 Years (Adult, Older Adult) 

 

 

 

##  Interventions 

Other

### Ofatumumab



There is no treatment allocation. Ofatumumab will be prescribed by the physician as per locally approved label. No drug will be dispensed from Novartis

 



 

 

 

##  Eligibility Criteria 

Inclusion Criteria:

To participate in the study, all the following inclusion criteria must be met:

\* Patients aged 18 years or older  
\* Written informed consent obtained before participating in the study.  
\* Patient is willing and able to complete the assessments, including PRO questionnaires, as outlined in this study.  
\* Diagnosis of RMS per McDonald Criteria (2017) occurred prior to initiation of Ofatumumab.  
\* Treatment with Ofatumumab is in accordance with the Portuguese indication of Kesimpta® (i.e., treatment of adult patients with relapsing multiple sclerosis (RMS) with active disease defined by clinical or imaging features).  
\* Patients that have initiated Ofatumumab up to 12 M prior inclusion in the study OR Patients that are initiating Ofatumumab at the moment of study inclusion.

Exclusion Criteria:

To participate in the study, none of the following exclusion criteria must be met:

\* Use of investigational drugs during the study, OR between Ofatumumab initiation and inclusion into the study, OR within 5 half-lives of investigational drug before Ofatumumab initiation, OR until the expected pharmacodynamic effect has returned to baseline, whichever is longer.  
\* Use of high efficacy therapy (including Ocrelizumab, Natalizumab, Mitoxantrone, Rituximab and Alemtuzumab) in both cohorts prior to the initiation of Ofatumumab.



 

 Portugal 

####  Novartis Investigative Site 

Recruiting

 Amadora,2720-276,Portugal

 

 

 

 

####  Novartis Investigative Site 

Recruiting

 Porto,4200 319,Portugal

 

 

 

 

####  Novartis Investigative Site 

Recruiting

 Guimarães,4835-044,Portugal

 

 

 

 

####  Novartis Investigative Site 

Recruiting

 Lisbon,1349-019,Portugal

 

 

 

 

####  Novartis Investigative Site 

Recruiting

 Leiria,2410-197,Portugal

 

 

 

 

####  Novartis Investigative Site 

Recruiting

 Lisbon,1169-050,Portugal

 

 

 

 

####  Novartis Investigative Site 

Recruiting

 Lisbon,1649-035,Portugal

 

 

 

 

####  Novartis Investigative Site 

Recruiting

 Matosinhos Municipality,4454-513,Portugal

 

 

 

 

####  Novartis Investigative Site 

Recruiting

 Ponte de Lima,4990-041,Portugal

 

 

 

 

####  Novartis Investigative Site 

Recruiting

 Setúbal,2910-549,Portugal

 

 

 

 

 

 

 

 

 

##  Worldwide Contacts 

If the location of your choosing does not feature any contact detail, please reach out using the information below.

#### Novartis Pharmaceuticals

Phone: [ +41613241111](tel:+41613241111) 

Email: <novartis.email@novartis.com>