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 1b clinical study of ICP-189 combined with furmonertinib in patients with advanced non-small cell lung cancer (NSCLC)

Trial Profile

A phase 1b clinical study of ICP-189 combined with furmonertinib in patients with advanced non-small cell lung cancer (NSCLC)

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 21 Nov 2024

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 Firmonertinib (Primary) ; ICP-189 (Primary)
  • Indications Non-small cell lung cancer
  • Focus Adverse reactions; Therapeutic Use

Most Recent Events

  • 14 Nov 2024 According to ArriVent Biopharma media release, initiation of dose expansion cohort for the ongoing Phase 1b trial evaluating firmonertinib in combination with SHP2 inhibitor ICP-189 by InnoCare in patients with classical EGFR mutations expected in the fourth quarter of 2024.
  • 29 Mar 2024 Status changed from planning to recruiting, according to an InnoCare Pharma media release.
  • 29 Mar 2024 According to an InnoCare Pharma media release, first patient in China has been dosed.

You need to be a logged in or subscribed to view this content

Request demo (opens in a new window)
If your organization or you do not have a subscription, try one of the following: 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