Our Vision
Red Queen Therapeutics is a clinical-stage company working to deliver important and accessible treatment options for a broad range of virus-borne illnesses including influenzas, coronaviruses, and other current and emerging pathogens.
Red Queen develops therapeutics based on a novel stapled lipopeptide platform technology that blocks virus-cell fusion—the way in which all enveloped viruses, including many of the most dangerous human pathogens, enter cells. As the viral load increases, illness ensues and the likelihood of transmission to others grows. Our stapled lipopeptides are designed to arrest this process, thereby halting disease progression, decreasing transmission and ultimately hastening viral clearance.
Red Queen’s stapled lipopeptide fusion inhibitors represent a new mode of early intervention that offers important advantages beyond available therapies. Our antiviral therapies are designed to:
Our novel antiviral platform is built on pioneering research conducted at the Walensky Lab at the Dana-Farber Cancer Institute under the leadership of Red Queen scientific co-founder Loren Walensky, MD, PhD and translated into a clinically tested therapeutic solution by Red Queen scientists.
Phase 1 trial results for Red Queen’s lead program RQ-01, administered intranasally in COVID-19 patients, showed placebo-like safety and evidence of efficacy, with accelerated viral clearance across multiple SARS-CoV-2 variants. These results offer proof-of-concept in humans for Red Queen’s antiviral platform.
Our platform, based on stapled lipopeptide mimics, can be rapidly customized and deployed against a broad range of viruses.
Our therapeutic platform is built on novel stapled helical peptide chemistry
2. Insert non-natural
amino acids
3. Chemically "staple" the peptide
1. Unstructured peptide
4. Stapled peptide
Hydrocarbon double-stapling remedies the proteolytic instability of a lengthy peptide therapeutic (Proceedings of the National Academy of Sciences, July 2010)
Distinct BimBH3 (BimSAHB) stapled peptides for structural and cellular studies (ACS Chemical Biology, January 2014)
Hydrocarbon-stapled peptides: principles, practice, and progress (Journal of Medicinal Chemistry, March 2014)
Mucosal delivery of a double-stapled RSV peptide prevents nasopulmonary infection (Journal of Clinical Investigation, April 2014)
A stapled lipopeptide platform for preventing and treating highly pathogenic viruses of pandemic potential (Nature Communications, January 2024)
Phase 1 Study of Intranasal Fusion Inhibitor RQ-01 for the Treatment of COVID-19 (ASM Microbe 2024 poster presentation, June 2024)
Red Queen is advancing programs across a range of viral diseases.
PROGRAM
INDICATION
DISCOVERY
PRECLINICAL
PHASE 1
PHASE 2
RQ-01
SARS-CoV-2
RQ-02
RSV / hMPV / PIV*
RQ-03**
Pan-Influenza
RQ-04
Herpes
* PIV-1, PIV-2, PIV-3, PIV-4, RSV (A and B), hMPV (A and B)
** BARDA-supported program
Red Queen lipopeptides are designed to be used as monotherapy or in combination with each other and/or other antivirals. They are amenable to a variety of administration routes including, among others, nasal and pulmonary.
November 22, 2024
If you are interested in learning more about Red Queen or would like to collaborate with us, please reach out below.
Please be aware that emails from any domain other than @redqueentx.com purporting to be from Red Queen Therapeutics (whether “job offers” or other communications) were not sent by Red Queen Therapeutics and are likely scams. Please do not reply to such messages or provide any personal information in response to them. There is no need to report the messages to Red Queen Therapeutics.
* All fields are required