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 I Dose-Escalation Study to Determine the Safety and Tolerability of an Intratumoural Injection of EBC-46

Trial Profile

Phase I Dose-Escalation Study to Determine the Safety and Tolerability of an Intratumoural Injection of EBC-46

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 05 Jun 2023

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 Tigilanol tiglate (Primary)
  • Indications Solid tumours
  • Focus Adverse reactions; First in man
  • Sponsors QBiotics

Most Recent Events

  • 31 May 2023 According to a QBiotics Group Limited media release, the safety and efficacy data from this study will be presented at the Sachs 9th Annual Immuno-Oncology Innovation Forum and the BIO International Convention, both being held in the US through June 2023, by Richard Godfrey.
  • 12 Aug 2020 Results published in the QBiotics Media Release
  • 09 Dec 2019 According to a QBiotics media release, results from this trial have been published in the journal EBioMedicine (a peer-reviewed research journal by The Lancet.)

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