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Multiple Sclerosis Patient Experience on Kesimpta and Ocrevus Subcutaneous Formulation

Multiple Sclerosis Patient Experience on Kesimpta and Ocrevus Subcutaneous Formulation

Non Recruiting
18-99 years
All
Phase N/A

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Overview

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

Eligibility

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

Study details
    Multiple Sclerosis

NCT06668324

Novartis Pharmaceuticals

21 October 2025

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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