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, Randomized, Double-blind, Placebo-controlled, Single Ascending Dose Study to Assess the Safety, Tolerability, and Pharmacokinetics of Apramycin Administered Intravenously in Healthy Adults.

Next Previous
Trial Profile

A Phase I, Randomized, Double-blind, Placebo-controlled, Single Ascending Dose Study to Assess the Safety, Tolerability, and Pharmacokinetics of Apramycin Administered Intravenously in Healthy Adults.

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 26 Jul 2022

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 Apramycin (Primary)
  • Indications Gram-negative infections
  • Focus Adverse reactions; First in man
  • Sponsors Juvabis Therapeutics

Most Recent Events

  • 18 Jul 2022 Results evaluating a population pharmacokinetic (PPK) analysis and predict an efficacious dose, published in the Journal of Antimicrobial Chemotherapy.
  • 10 Nov 2020 Status changed from recruiting to completed.
  • 02 Jul 2020 Planned number of patients changed from 32 to 40.

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