Last Update: Jun 02, 2025
Multiple Sclerosis Patient Experience on Kesimpta and Ocrevus Subcutaneous Formulation (MS-PEKOS)
ClinicalTrials.gov Identifier:
Novartis Reference Number:COMB157AUS25
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

The study aims to compare the experiences, including injection-related reactions (IRRs) of patients newly receiving ofatumumab to those starting to receive ocrelizumab SC formulation

Multiple Sclerosis
Recruiting
100
Nov 15, 2024
Aug 29, 2025
All
18 Years - 99 Years (Adult, Older Adult)

Eligibility Criteria

Inclusion Criteria:

1. Ability to use a mobile device or computer with broadband internet access (or data streaming available)
2. Ability to read, understand, and respond in English
3. Adult aged 18 years of age or over at the time of the survey
4. Self-confirmed diagnosis of MS
5. Prescribed either OMB or OCR SC and will receive their first injection (Day 0) followed by completing the study survey between Day 1 and Day 7

Exclusion Criteria:

1. Participated in an OMB or OCR randomized clinical trial
2. Previously treated with OMB or OCR SC
3. Cognitive impairment that impacts the patient's ability to participate in a survey study

Novartis Investigative site

Recruiting

East Hanover,New Jersey,07936,United States

Worldwide Contacts

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Novartis Pharmaceuticals