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 Randomized, Single-Blind, Parallel Group, Placebo-Controlled, Dose Rate Escalation Study Evaluating the Safety and Effects of MN-221 [bedoradrine] in Subjects Diagnosed With Moderate to Severe Asthma.

Next Previous
X
Search
Trial Profile

A Randomized, Single-Blind, Parallel Group, Placebo-Controlled, Dose Rate Escalation Study Evaluating the Safety and Effects of MN-221 [bedoradrine] in Subjects Diagnosed With Moderate to Severe Asthma.

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 13 Aug 2013

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 Bedoradrine (Primary)
  • Indications Asthma
  • Focus Adverse reactions; Therapeutic Use

    • Most Recent Events

    • 12 Nov 2012 Results published in the the Journal of Asthma, according to a MediciNova media release.
    • 02 Mar 2011 Status changed from active, no longer recruiting to completed.
    • 28 Oct 2010 Data were presented at the 2010 Annual Meeting of the American College of Chest Physicians, according to a MediciNova media release.

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