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?

An efficacy and safety study of Pixavir

Trial Profile

An efficacy and safety study of Pixavir

Status: Planning
Phase of Trial: Phase I

Latest Information Update: 31 Jul 2025

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 Pixavir (Primary)
  • Indications Influenza virus infections
  • Focus Adverse reactions; Therapeutic Use

Most Recent Events

  • 31 Jul 2025 New trial record
  • 20 Jun 2025 According to the TaiGen Biotechnology Media Release, the company announced on the evening of the 19th that it received a notice from its partner Jianxingyuan Pharmaceutical Group that the new influenza antiviral drug Pixavir marboxil (TG-1000) has passed the clinical trial review (IND) of pediatric dosage forms of the National Medical Products Administration (NMPA) of Chinese mainland and will start clinical trials soon.
  • 20 Jun 2025 According to the TaiGen Biotechnology Media Release, efficacy and safety trial planned for Q4 2025.

You need to be a logged in or subscribed to view this content

Request demo (opens in a new window)
If your organization or you do not have a subscription, try one of the following: 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