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 single-center, randomized, double-blind, placebo-controlled multiple-ascending dose study of QX002N injection in subjects with ankylosing spondylitis

X
Trial Profile

A single-center, randomized, double-blind, placebo-controlled multiple-ascending dose study of QX002N injection in subjects with ankylosing spondylitis

Status: Not yet recruiting
Phase of Trial: Phase I

Latest Information Update: 04 Aug 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 QX 002N (Primary)
  • Indications Ankylosing spondylitis
  • Focus Adverse reactions; Pharmacokinetics
  • Most Recent Events

    • 03 Aug 2020 As per Clinical trial registry front page of this trial, date of first enrolment is given as 1 Aug 2020 (no clear info if this is the date when actual enrolment has begin), while as per inside view of trial record, Overall status is not yet recruiting (last updated on June 2020).Retaining status as not yet recruiting based on this for now.Pls update further.
    • 03 Aug 2020 New trial record

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