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 1 open-label study of the safety and feasibility of ZYC300 administration with cyclophosphamide pre-dosing.

X
Trial Profile

A phase 1 open-label study of the safety and feasibility of ZYC300 administration with cyclophosphamide pre-dosing.

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 17 May 2013

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 ZYC 300 (Primary) ; Cyclophosphamide
  • Indications Breast cancer; Colon cancer; Ovarian cancer; Prostate cancer; Renal cancer; Various toxicities
  • Focus Adverse reactions
  • Most Recent Events

    • 12 May 2009 Actual patient number (22) added as reported by ClinicalTrials.gov.
    • 12 May 2009 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.
    • 24 Oct 2008 Study sponsor changed from MGI Pharma to Eisai Medical Research, based on information from ClinicalTrials.gov.

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