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?

Phase I Study of CCI-779 (NSC 683864, IND 61010) in Combination With Carboplatin and Paclitaxel in Patients With Advanced Solid Tumours

Next Previous
X
Search
Trial Profile

Phase I Study of CCI-779 (NSC 683864, IND 61010) in Combination With Carboplatin and Paclitaxel in Patients With Advanced Solid Tumours

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 21 Mar 2016

Price : $35 *
  • 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 Temsirolimus (Primary) ; Carboplatin; Paclitaxel
  • Indications Endometrial cancer; Ovarian cancer; Solid tumours
  • Focus Adverse reactions

    • Most Recent Events

    • 08 Aug 2011 Planned end date changed from 1 Apr 2009 to 1 Nov 2011 as reported by ClinicalTrials.gov.
    • 08 Apr 2009 Status changed from recruiting to active, no longer recruiting as reported by ClinicalTrials.gov.
    • 21 Jan 2009 Status changed from suspended to recruiting according to both the ClinicalTrials.gov record and the National Cancer Institute of Canada record.

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