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Intellectual Property
Securing the Future: Building a Strong IP Estate in RNAa and Oligonucleotide Delivery 

Intellectual Property

At the heart of Ractigen Therapeutics lies a strong intellectual property (IP) foundation, notably in the fields of RNA activation (RNAa) and oligonucleotide delivery. Central to our innovation is a high-throughput discovery engine, expertly designed for the swift identification of small activating RNAs (saRNAs). Our IP portfolio is strategically constructed upon both the composition of matter and methods of use, encompassing an expanding library of therapeutic oligonucleotides. The development of proprietary medicinal chemistries and delivery platforms, all created in-house, further solidifies our IP estate, providing a robust platform for advanced drug development

High-Throughput
Process

Our Discovery Engine

It features a highly-refined bioinformatics algorithm integrating epigenetic datasets, design rules, and genome-wide on-target prediction tethered to in-house oligonucleotide manufacturing for saRNA synthesis followed by automated experimental validation of saRNA activity.

Labeled arrows: Genetic Sequence, Target Identification, saRNA Synthesis, and HTS
Target Gene Locus icon

Target Gene Locus

Rapidly identify all saRNAs for any single target gene

Search Algorithm icon

Search Algorithm

Highly-refined
bioinformatics algorithm

In-House Synthesis icon

In-House Synthesis

Oligonucleotide manufacturing for in-house saRNA synthesis

In vitro Screening & Gene Expression icon

In vitro Screening & Gene Expression

Automated rounds of dose-dependent gene expression

3-4 Weeks Start to Finish (All In-House)

Start to finish underline

Screen Hundreds of saRNA Candidates

Automated rounds of dose-dependent gene expression analytics and integrated de-risking safety assays allow for the screening of hundreds of saRNA candidates within 30-45 days.

Honing the Process

We are continually honing the process in pursuit of full-automation and continue to add to our ever-growing list of therapeutic genes expanding our IP estate and feeding our drug development pipeline.

Want to Discover More?

Check out our News. Below are some highlights to get you started.

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November 19, 2024 in Homepage News, News Highlight

Ractigen Therapeutics Announces FDA Orphan Drug Designation for RAG-21 for the Treatment of ALS

NANTONG and SUZHOU, China, Nov. 19, 2024 — Ractigen Therapeutics, a clinical-stage pharmaceutical company dedicated…
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October 11, 2024 in Presentations, RAG-01 Presentation

Development and Clinical Progress of RAG-01, a Novel saRNA Targeting p21 for Non-Muscle Invasive Bladder Cancer Treatment. (Abstract)

Event: 2024 Oligonucleotide Therapeutics Society Meeting (Montreal) View Abstract
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September 10, 2024 in Company News, RAG-17

Ractigen Announces Positive Clinical Data for RAG-17 in ALS-SOD1 Treatment from Investigator-Initiated Trial

NANTONG and SUZHOU, China, Sep.10, 2024 — Ractigen Therapeutics, a clinical-stage pharmaceutical company dedicated to…
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August 22, 2024 in Company News

Ractigen Therapeutics Announces U.S. FDA Orphan Drug Designation (ODD) granted to RAG-18 for the treatment of Duchenne Muscular Dystrophy and Becker Muscular Dystrophy

JIANGSU, China, August 22, 2024 – Ractigen Therapeutics, a pioneering developer of small activating RNA…
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