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 Placebo Controlled Trial Assessing Effect of Intensive HAART With Raltegravir, and Maraviroc,on HIV-1 Pro-viral DNA and Reservoir Decay in HIV-1-infected Individuals Initiating ART During the Acute Phase of Infection.

Next Previous
Trial Profile

Randomized Placebo Controlled Trial Assessing Effect of Intensive HAART With Raltegravir, and Maraviroc,on HIV-1 Pro-viral DNA and Reservoir Decay in HIV-1-infected Individuals Initiating ART During the Acute Phase of Infection.

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

Latest Information Update: 18 Sep 2021

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 Antiretrovirals; Emtricitabine/tenofovir disoproxil fumarate; Lopinavir/ritonavir; Maraviroc; Raltegravir
  • Indications HIV-1 infections
  • Focus Therapeutic Use

Most Recent Events

  • 05 Apr 2016 Biomarkers information updated
  • 28 May 2013 Status changed from not yet recruiting to active, no longer recruiting as reported by ClinicalTrials.gov.
  • 28 May 2013 Status changed from not yet recruiting to active, no longer recruiting as reported by ClinicalTrials.gov.

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