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?

An Alternative Phase I Clinical Trial to Evaluate Tegoprazan Tablets in the U.S.

X
Trial Profile

An Alternative Phase I Clinical Trial to Evaluate Tegoprazan Tablets in the U.S.

Status: Planning
Phase of Trial: Phase I

Latest Information Update: 03 Jul 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 Tegoprazan (Primary)
  • Indications Gastro-oesophageal reflux
  • Focus Adverse reactions
  • Sponsors HK inno.N
  • Most Recent Events

    • 03 Jul 2020 New trial record
    • 18 Jun 2020 According to a RaQualia Innovations media release, the U.S. Food and Drug Administration (FDA) has approved the Investigational New Drug (IND) application for tegoprazan (RQ-00000004/CJ-12420/K-CAB, hereinafter called tegoprazan) for the treatment of gastroesophageal reflux disease.HK inno.N plans to conduct an alternative Phase I clinical trial to facilitate the development in the U.S. by using tegoprazan tablets that have been already marketed in Korea.

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