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 1, Multicenter, Randomized, Double-blind, Placebo- Controlled, Parallel Group Study to Evaluate the Safety of RQ-01 in SARS-CoV-2 Positive Subjects

Trial Profile

A Phase 1, Multicenter, Randomized, Double-blind, Placebo- Controlled, Parallel Group Study to Evaluate the Safety of RQ-01 in SARS-CoV-2 Positive Subjects

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 04 Dec 2024

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 RQ 01 (Primary)
  • Indications COVID 2019 infections
  • Focus Adverse reactions; First in man
  • Sponsors Red Queen Therapeutics

Most Recent Events

  • 03 Dec 2024 According to Red Queen Therapeutics media release, based on results from this study company has been working with the U.S. Food and Drug Administration (FDA) on a clinical development/registration plan for RQ-01 focused on treatment in combination with standard-of-care therapy, including antivirals, in high-risk immunocompromised patients.
  • 06 Aug 2024 Results presented in the Apple Tree Partners Media Release.
  • 16 Jun 2024 According to an Apple Tree Partners media release, the results from this trial were presented at the American Society for Microbiology (ASM) Microbe annual meeting.

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