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 I study of the combination of daily oral pazopanib with intravenous ifosfamide in patients with advanced solid malignancies.

Trial Profile

A phase I study of the combination of daily oral pazopanib with intravenous ifosfamide in patients with advanced solid malignancies.

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 29 Jan 2025

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 Ifosfamide (Primary) ; Pazopanib (Primary)
  • Indications Solid tumours
  • Focus Adverse reactions; Biomarker
  • Acronyms Pazi

Most Recent Events

  • 01 Jan 2025 Results (n=49) from two different studies The patients investigated were drawn from two studies on IFO with coadministration of pazopanib or sunitinib conducted in Erasmus University Medical Center, Erasmus MC Cancer Institute, Rotterdam, assessing peripheral and central neurotoxicity, caused by this drug combination published in the Biomedicine and Pharmacotherapy
  • 16 Nov 2015 Status changed from recruiting to completed.
  • 06 Nov 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