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 Phase III Study Comparing Low Dose Cyclosporine, Methotrexate And Prednisone Versus Standard Dose Cyclosporine and Methotrexate As Graft Versus Host Disease Prophylaxis In Myeloablative Allogeneic Stem Cell Transplantation (ALLG BM10 trial) in patients with haematological malignancies

Trial Profile

A Phase III Study Comparing Low Dose Cyclosporine, Methotrexate And Prednisone Versus Standard Dose Cyclosporine and Methotrexate As Graft Versus Host Disease Prophylaxis In Myeloablative Allogeneic Stem Cell Transplantation (ALLG BM10 trial) in patients with haematological malignancies

Status: Withdrawn prior to enrolment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

Latest Information Update: 22 Jun 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 Prednisone (Primary) ; Ciclosporin; Ciclosporin
  • Indications Graft-versus-host disease
  • Focus Therapeutic Use

Most Recent Events

  • 18 Jun 2021 Status changed from completed to withdrawn prior to enrolment.
  • 08 Jun 2016 Status changed from not yet recruiting to completed.
  • 14 May 2009 New trial record

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