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?

Study assessing mechanisms of resistance to almonertinib and characterize clinically patients with EGFR-mutant lung cancers who had next-generation sequencing performed on tumor tissue or plasma after developing acquired resistance to almonertinib

Next Previous
Search
Trial Profile

Study assessing mechanisms of resistance to almonertinib and characterize clinically patients with EGFR-mutant lung cancers who had next-generation sequencing performed on tumor tissue or plasma after developing acquired resistance to almonertinib

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 28 Oct 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 Aumolertinib (Primary)
  • Indications Non-small cell lung cancer
  • Focus Therapeutic Use

    • Most Recent Events

    • 28 Oct 2022 New trial record
    • 13 Sep 2022 Results presented at the 47th European Society for Medical Oncology Congress

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