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?

An observational study assessing the single-center experience experience with new disease-modifying terapy (DMT) and its clinical outcomes in patients with Multople Sclerosis at the demyelinating diseases unit from the Hospital de Clínicas-UNA

Next Previous
X
Search
Trial Profile

An observational study assessing the single-center experience experience with new disease-modifying terapy (DMT) and its clinical outcomes in patients with Multople Sclerosis at the demyelinating diseases unit from the Hospital de Clínicas-UNA

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 26 Mar 2021

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 Alemtuzumab (Primary) ; Interferon (Primary) ; Ocrelizumab (Primary) ; Rituximab (Primary)
  • Indications Multiple sclerosis
  • Focus Adverse reactions; Therapeutic Use

    • Most Recent Events

    • 26 Mar 2021 New trial record
    • 27 Feb 2021 Results presented at the Americas Committee for Treatment and Research in Multiple Sclerosis Forum 2021

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