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?

Phase 1 Clinical trial of MAN-19 intended to treat complications caused by COVID-19

Trial Profile

Phase 1 Clinical trial of MAN-19 intended to treat complications caused by COVID-19

Status: Planning
Phase of Trial: Phase I

Latest Information Update: 31 Dec 2021

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 MAN-19 (Primary)
  • Indications COVID 2019 infections; SARS-CoV-2 acute respiratory disease
  • Focus Adverse reactions

Most Recent Events

  • 29 Dec 2020 According to a Q BioMed media release, the Investigational New Drug (IND) application (or similar clinical trial proposal) to regulators is planned for the first quarter of 2021. This trial is planned to commencing in the first half of 2021.
  • 26 Aug 2020 According to a Q BioMed media release, the Phase 1 clinical trial is slated to begin patient enrollment in February 2021 supported by Canadian Government
  • 30 Jun 2020 According to a Q BioMed media release, an Investigational New Drug (IND) application (or similar clinical trial proposal) to regulators are planned for late 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