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?

Randomized Phase II Trial of S-1 Versus S-1 plus Oxaliplatin (Sox) in Patients with Gemcitabine Refractory Pancreatic Cancer

Trial Profile

Randomized Phase II Trial of S-1 Versus S-1 plus Oxaliplatin (Sox) in Patients with Gemcitabine Refractory Pancreatic Cancer

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 27 Jun 2017

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 Oxaliplatin (Primary) ; Gimeracil/oteracil/tegafur
  • Indications Adenosquamous carcinoma; Pancreatic cancer
  • Focus Therapeutic Use
  • Sponsors Yakult Honsha

Most Recent Events

  • 06 Jun 2017 Results of pooled analysis of three studies including this study presented at the 53rd Annual Meeting of the American Society of Clinical Oncology
  • 31 May 2013 According to a Yakult Honsha media release, the company has submitted supplemental new drug applications relating to an additional indication for pancreatic cancer, with respect to its products, Campto (40mg and 100mg), Elplat (50mg, 100mg and 200mg), and Levofolinate [Yakult] (25mg and 100mg), to the Japanese Ministry of Health, Labor and Welfare (MHLW).
  • 30 Oct 2012 New trial record

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