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 phase II trial of fixed-dose combination of trabodenoson and latanoprost for the treatment of open-angle glaucoma and/or ocular hypertension

Next Previous
X
Search
Trial Profile

A phase II trial of fixed-dose combination of trabodenoson and latanoprost for the treatment of open-angle glaucoma and/or ocular hypertension

Status: Active, no longer recruiting
Phase of Trial: Phase II

Latest Information Update: 17 May 2017

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 Latanoprost/trabodenoson (Primary)
  • Indications Ocular hypertension; Open-angle glaucoma
  • Focus Therapeutic Use
  • Sponsors Inotek Pharmaceuticals

    • Most Recent Events

    • 10 May 2017 According to an Inotek Pharmaceuticals media release, top-line results from this trial are expected in July 2017.
    • 20 Mar 2017 New trial record
    • 16 Mar 2017 According to an Inotek Pharmaceuticals media release, status changed from recruiting to active, no longer recruiting.

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