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 phase I/II safety, tolerability, and pharmacokinetic study of high dose lopinavir/ritonavir with or without saquinavir in HIV-infected pediatric subjects previously treated with protease inhibitors

Next Previous
X
Search
Trial Profile

A phase I/II safety, tolerability, and pharmacokinetic study of high dose lopinavir/ritonavir with or without saquinavir in HIV-infected pediatric subjects previously treated with protease inhibitors

Status: Completed
Phase of Trial: Phase I/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 Lopinavir/ritonavir (Primary) ; Saquinavir (Primary)
  • Indications HIV infections
  • Focus Adverse reactions; Therapeutic Use

    • Most Recent Events

    • 03 Apr 2012 Actual patient number is 26 according to ClinicalTrials.gov.
    • 28 Sep 2008 The actual trial end date is 1 Dec 2006 according to ClinicalTrials.gov record.
    • 28 Sep 2008 Status changed from active, no longer recruiting to completed according to ClinicalTrials.gov 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