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?

Phase I Evaluation of Sodium Stibogluconate [VQD 001; VioQuest Pharmaceuticals] in Combination With Interferon alpha-2b for Solid Tumors, Lymphoma or Myeloma.

X
Trial Profile

Phase I Evaluation of Sodium Stibogluconate [VQD 001; VioQuest Pharmaceuticals] in Combination With Interferon alpha-2b for Solid Tumors, Lymphoma or Myeloma.

Status: Completed
Phase of Trial: Phase I

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 Interferon alpha-2b (Primary) ; Sodium stibogluconate (Primary)
  • Indications Lymphoma; Multiple myeloma; Solid tumours
  • Focus Adverse reactions; Therapeutic Use
  • Most Recent Events

    • 21 Nov 2009 Planned number of patients changed from 24 to 54 as reported by M.D. Anderson Cancer Center record.
    • 30 Jun 2009 Trial phase changed from I/II to I and additional lead trial centre as reported by ClinicalTrials.gov.
    • 11 Jun 2008 Status changed from in progress to completed as reported by VioQuest Pharmaceuticals.

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