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 Retrospective Study to Evaluate the Safety and Efficacy of Paclitaxel Combined with Ramucirumab as Second Line Therapy in Japanese Patients with Advanced Gastric Cancer

Next Previous
X
Search
Trial Profile

A Retrospective Study to Evaluate the Safety and Efficacy of Paclitaxel Combined with Ramucirumab as Second Line Therapy in Japanese Patients with Advanced Gastric Cancer

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 26 Jun 2018

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 Paclitaxel (Primary) ; Ramucirumab (Primary)
  • Indications Gastric cancer
  • Focus Adverse reactions; Therapeutic Use

    • Most Recent Events

    • 05 Jun 2018 Results comparing paclitaxel combined with ramucirumab as the second-line chemotherapy in younger patients versus elderly patients with advanced gastric cancer, presented at the 54th Annual Meeting of the American Society of Clinical Oncology.
    • 21 Jun 2017 New trial record
    • 06 Jun 2017 Results (n=18) presented at the 53rd Annual Meeting of the American Society of Clinical Oncology.

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