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 prospectively randomized, phase III, multicenter, controlled trial to evaluate the safety and efficacy of the Zevalin [ibritumomab tiuxetan Y-90] therapeutic regimen plus Rituxan [rituximab] compared with Rituxan alone in patients with relapsed or refractory follicular NHL [non-Hodgkin's lymphoma]

Next Previous
X
Search
Trial Profile

A prospectively randomized, phase III, multicenter, controlled trial to evaluate the safety and efficacy of the Zevalin [ibritumomab tiuxetan Y-90] therapeutic regimen plus Rituxan [rituximab] compared with Rituxan alone in patients with relapsed or refractory follicular NHL [non-Hodgkin's lymphoma]

Status: Discontinued
Phase of Trial: Phase III

Latest Information Update: 03 Nov 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 Ibritumomab tiuxetan (Primary) ; Rituximab (Primary)
  • Indications Non-Hodgkin's lymphoma
  • Focus Therapeutic Use

    • Most Recent Events

    • 02 Oct 2006 Status change
    • 23 Sep 2005 New trial record.

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