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 retrospective, cohort study comparing the hematologic safety profile of linezolid versus tedizolid for the treatment of Nontuberculous Mycobacteria in solid organ transplant (SOT) recipients

Next Previous
Trial Profile

A retrospective, cohort study comparing the hematologic safety profile of linezolid versus tedizolid for the treatment of Nontuberculous Mycobacteria in solid organ transplant (SOT) recipients

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 17 Dec 2020

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 Linezolid (Primary) ; Tedizolid (Primary)
  • Indications Nontuberculous mycobacterium infections
  • Focus Adverse reactions

Most Recent Events

  • 17 Dec 2020 New trial record
  • 25 Oct 2020 Results (n=12) assessing clinical efficacy of tedizolid for the treatment of mycobacterium abscessus complex infections in solid organ transplant recipients, presented at the IDWeek 2020
  • 25 Oct 2020 Primary endpoint . (the hematologic effects of linezolid versus tedizolid from therapy initiation to week seven) has not been met as per results presented at the IDWeek 2020

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