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 Randomized, Phase III Study of Fotemustine Versus the Combination of Fotemustine and Ipilimumab or the Combination of Ipilimumab and Nivolumab in Patients With Metastatic Melanoma With Brain Metastasis

Trial Profile

A Randomized, Phase III Study of Fotemustine Versus the Combination of Fotemustine and Ipilimumab or the Combination of Ipilimumab and Nivolumab in Patients With Metastatic Melanoma With Brain Metastasis

Status: Discontinued
Phase of Trial: Phase III

Latest Information Update: 11 Mar 2024

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 Ipilimumab (Primary) ; Fotemustine; Nivolumab
  • Indications Brain metastases; Malignant melanoma
  • Focus Therapeutic Use
  • Acronyms NIBIT-M2

Most Recent Events

  • 08 Mar 2024 Status changed from recruiting to discontinued.
  • 24 Oct 2023 Results (As of May 1, 2023, n=80; 7-year outcomes) assessing efficacy of Nivolumab plus ipilimumab in melanoma patients with asymptomatic brain metastases presented at the 48th European Society for Medical Oncology Congress
  • 10 Jun 2021 Results of an interim analysis published in the Clinical Cancer Research

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

Request demo (opens in a new window)
If your organization or you do not have a subscription, try one of the following: 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