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?

Multicenter Retrospective Study of the Effectiveness and Safety of Darunavir/Cobicistat (DRV/c) Containing Regimens in Routine Clinical Practice

X
Trial Profile

Multicenter Retrospective Study of the Effectiveness and Safety of Darunavir/Cobicistat (DRV/c) Containing Regimens in Routine Clinical Practice

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 05 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 Cobicistat/darunavir (Primary) ; Dolutegravir; Rilpivirine
  • Indications HIV-1 infections
  • Focus Therapeutic Use
  • Acronyms CoDAR
  • Most Recent Events

    • 27 Jan 2021 Results (n=725) assessing changes in creatinine estimated glomerular filtration rate, published in the Journal of Antimicrobial Chemotherapy.
    • 05 Oct 2019 Results determining the characteristics of darunavir/cobicistat use in HIV-infected adults in Spain published in the Journal of Antimicrobial Chemotherapy
    • 24 Jun 2019 Results published in the Journal of Antimicrobial Chemotherapy

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