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 randomized, single-dose, double-blind, crossover study to evaluate safety, tolerability, pharmacodynamics, and pharmacokinetics of IMB-115 alone and in combination with alcohol in healthy subjects

X
Trial Profile

A randomized, single-dose, double-blind, crossover study to evaluate safety, tolerability, pharmacodynamics, and pharmacokinetics of IMB-115 alone and in combination with alcohol in healthy subjects

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 02 Sep 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 Sunobinop (Primary) ; Alcohol
  • Indications Insomnia
  • Focus Adverse reactions; Pharmacodynamics; Pharmacokinetics
  • Sponsors Imbrium Therapeutics
  • Most Recent Events

    • 28 Aug 2020 According to an Imbrium Therapeutics media release, data from this study were shared at the 34th Annual Meeting of the Associated Professional Sleep Societies (SLEEP 2020).
    • 01 Jul 2019 New trial record
    • 25 Jun 2019 Results published in the Media Release

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