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?

Romiplostim for Thrombocytopenia Induced by Lomustine at First Progression of MGMT Promoter-methylated Glioblastoma: a Randomized Phase II Open Label Multicenter Study

X
Trial Profile

Romiplostim for Thrombocytopenia Induced by Lomustine at First Progression of MGMT Promoter-methylated Glioblastoma: a Randomized Phase II Open Label Multicenter Study

Status: Withdrawn prior to enrolment
Phase of Trial: Phase II

Latest Information Update: 25 Sep 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 Romiplostim (Primary) ; Lomustine
  • Indications Chemotherapy-induced damage; Thrombocytopenia
  • Focus Therapeutic Use
  • Acronyms RIGOLETTO
  • Most Recent Events

    • 24 Sep 2023 This trial has been discontinued in Spain.
    • 13 Aug 2023 This trial has been discontinued in Italy (Date of the global end of the trial: 19 Dec 2022).
    • 23 May 2023 Status changed from recruiting to withdrawn prior to enrolment because Amgen withdrew interest in providing further financial support.

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