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 Rollover Study to Evaluate Safety and Therapeutic Effect of Re-Infusing Subjects Who Completed Participation in the VRX496-USA-05-002 Trial With Autologous T Cells Transduced With VRX496 [lexgenleucel-T].

Next Previous
X
Search
Trial Profile

A Rollover Study to Evaluate Safety and Therapeutic Effect of Re-Infusing Subjects Who Completed Participation in the VRX496-USA-05-002 Trial With Autologous T Cells Transduced With VRX496 [lexgenleucel-T].

Status: Active, no longer recruiting
Phase of Trial: Phase II

Latest Information Update: 05 Jun 2023

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 Lexgenleucel T (Primary)
  • Indications HIV infections
  • Focus Adverse reactions; Therapeutic Use

    • Most Recent Events

    • 05 Oct 2010 Planned end date changed from 1 Mar 2010 to 1 Jun 2023 as reported by ClinicalTrials.gov.
    • 05 Oct 2010 Status changed from recruiting to active, no longer recruiting as reported by ClinicalTrials.gov.
    • 04 Mar 2008 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