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 randomized, multicenter open label phase II study to determine the safety and efficacy of induction therapy with imatinib in comparison with standard induction chemotherapy in elderly (>55 years) patients with Ph positive acute lymphoblastic leukemia (ALL)

X
Trial Profile

A randomized, multicenter open label phase II study to determine the safety and efficacy of induction therapy with imatinib in comparison with standard induction chemotherapy in elderly (>55 years) patients with Ph positive acute lymphoblastic leukemia (ALL)

Status: Completed
Phase of Trial: Phase II

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 Imatinib (Primary) ; Cyclophosphamide; Cytarabine; Dexamethasone; Dexamethasone; Idarubicin; Methotrexate; Vincristine
  • Indications Precursor cell lymphoblastic leukaemia-lymphoma
  • Focus Therapeutic Use
  • Most Recent Events

    • 11 Apr 2007 Status changed to completed.
    • 22 Feb 2006 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