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 trial to study efficacy and safety of initial combination therapy with gemigliptin and metformin vs. gemigliptin or metformin monotherapy in drug-naïve patients with type 2 diabetes

X
Trial Profile

A trial to study efficacy and safety of initial combination therapy with gemigliptin and metformin vs. gemigliptin or metformin monotherapy in drug-naïve patients with type 2 diabetes

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 02 Jun 2016

Price : $35 *
  • 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 Gemigliptin/metformin (Primary) ; Gemigliptin; Metformin
  • Indications Type 2 diabetes mellitus
  • Focus Therapeutic Use
  • Most Recent Events

    • 02 Jun 2016 Primary endpoint (change from baseline in HbA1c after 24 weeks) has been met, according to results presented at The 98th Annual Meeting of the Endocrine Society
    • 02 Jun 2016 New trial record
    • 04 Apr 2016 Results presented at The 98th Annual Meeting of the Endocrine Society

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