Either you have JavaScript disabled or your browser does not support Javascript . To work properly, this page requires JavaScript to be enabled.
How to enable JavaScript in your browser?

A prospective nonrandomized controlled observational multicenter trial of mRNA vaccination in ocrelizumab-treated multiple sclerosis patients

Next Previous
X
Search
Trial Profile

A prospective nonrandomized controlled observational multicenter trial of mRNA vaccination in ocrelizumab-treated multiple sclerosis patients

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 14 Nov 2023

Price :

$35 *

Note:
  • Adis is an information provider.
  • Final gross price and currency may vary according to local VAT and billing address.
  • Your purchase entitles you to full access to the information contained in our trial profile at the time of purchase.
  • A link to download a PDF version of the trial profile will be included in your email receipt.

At a glance

  • Drugs Tozinameran (Primary)
  • Indications COVID 2019 infections
  • Focus Pharmacodynamics

    • Most Recent Events

    • 01 Nov 2023 Results assessing correlation between clinical outcomes with the humoral and cellular response, published in the Journal of Neurology, Neurosurgery and Psychiatry.
    • 16 Jun 2023 New trial record
    • 27 Apr 2023 Results presented at the 75th Annual Meeting of the American Academy of Neurology 2023

You need to be a logged in or subscribed to view this content Request demo

If your organization or you do not have a subscription, try one of the following:
  • Contacting your organization’s admin about adding this content to your AdisInsight subscription
  • Buying a PDF version of any individual profile
  • Request a free trial
If your organization has a subscription, there are several access options, even while working remotely:
  • Working within your organization’s network
  • with username/password or try to via your institution
  • Persisted access using your organization’s identifier stored in your user browser for 90 days
Back to top