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/II study of chemoprevention with epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor erlotinib (OSI-774, Tarceva) and cyclooxygenase-2 (COX-2) inhibitor (Celecoxib) in premalignant lesions of head and neck of former smokers.

Next Previous
X
Search
Trial Profile

Phase I/II study of chemoprevention with epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor erlotinib (OSI-774, Tarceva) and cyclooxygenase-2 (COX-2) inhibitor (Celecoxib) in premalignant lesions of head and neck of former smokers.

Status: Completed
Phase of Trial: Phase I/II

Latest Information Update: 17 Sep 2021

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 Celecoxib (Primary) ; Erlotinib (Primary)
  • Indications Head and neck cancer
  • Focus Adverse reactions; Therapeutic Use

    • Most Recent Events

    • 22 Feb 2013 Planned end date changed from 1 Oct 2015 to 1 Nov 2013 as reported by ClinicalTrials.gov.
    • 22 Feb 2013 Status changed from recruiting to active, no longer recruiting as reported by ClinicalTrials.gov.
    • 26 May 2011 Status changed from suspended to 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