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?

Multicenter phase II study evaluating docetaxel, CDDP [cisplatin], and cetuximab as induction regimen prior to surgery in chemo-naive patients with NSCLC [non-small cell lung cancer] stage IB, II and IIIA

Next Previous
X
Search
Trial Profile

Multicenter phase II study evaluating docetaxel, CDDP [cisplatin], and cetuximab as induction regimen prior to surgery in chemo-naive patients with NSCLC [non-small cell lung cancer] stage IB, II and IIIA

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 09 May 2022

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 Cetuximab (Primary) ; Cisplatin (Primary) ; Docetaxel (Primary)
  • Indications Non-small cell lung cancer
  • Focus Therapeutic Use

    • Most Recent Events

    • 28 Apr 2014 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov record.
    • 10 Mar 2011 Planned end date changed from 1 Dec 2009 to 1 Jun 2011 as reported by ClinicalTrials.gov.
    • 26 Aug 2010 Status changed from completed to active, no longer recruiting as reported by 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