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, Double-Blind, Placebo-Controlled, Single Ascending Dose Study to Describe Pharmacokinetics/Pharmacodynamics, and the Safety and of SPH3127 Tablet in Chinese Healthy Volunteers

Next Previous
X
Search
Trial Profile

A Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Study to Describe Pharmacokinetics/Pharmacodynamics, and the Safety and of SPH3127 Tablet in Chinese Healthy Volunteers

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 28 Mar 2022

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 SPH 3127 (Primary)
  • Indications Hypertension
  • Focus Adverse reactions
  • Sponsors Shanghai Pharmaceuticals Holding

    • Most Recent Events

    • 27 Feb 2021 Results of single and multiple ascending dose studies (NCT03128138 and NCT0325599), published in the Clinical Therapeutics
    • 27 Feb 2021 Status changed from recruiting to completed, as per results published in the Clinical Therapeutics.
    • 16 Jul 2017 Planned End Date changed from 1 Jul 2017 to 1 Jul 2018.

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