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 high-dose, intermittent sunitinib in patients with solid tumors

Next Previous
X
Search
Trial Profile

A phase I study of high-dose, intermittent sunitinib in patients with solid tumors

Status: Completed
Phase of Trial: Phase I/II

Latest Information Update: 08 Apr 2022

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 Sunitinib (Primary)
  • Indications Solid tumours
  • Focus Adverse reactions
  • Acronyms SUNRISE

    • Most Recent Events

    • 25 Oct 2020 Results evaluating tumor- and skin tissue drug concentrations of patients participating in this trial and related them to the plasma concentrations and clinical outcome presented at the 32nd EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics
    • 26 Dec 2018 Status changed from recruiting to completed, as reported in an article published in the Journal of Clinical Oncology.
    • 26 Dec 2018 Results published in the Journal of Clinical Oncology

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