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COMPANY RESEARCH

Ractigen Therapeutics

Develops RNA-activation and siRNA medicines. RAG-17 targets SOD1; its April 21, 2026 release reports Phase 1/2 and Phase 2 dosing, whereas its undated pipeline still says Phase 1.

Company at a glance

Corporate information

Company entity
Ractigen Therapeutics
Headquarters / principal office
Suzhou, China; company description ↗
Founded
2017 ↗
Ownership / capital status
PrivateCompany states over RMB350 million in venture capital, without an as-of date; not treated as its latest round. ↗
Official corporate reference
https://www.ractigen.com/ ↗
LinkedIn company page
Independent company page not verified

Profile review: 2026-11-07 · Fields retain their individual source dates. Undisclosed values are not zero; early or historical events do not establish the latest financing. Awards and acquisitions are distinguished from equity rounds.

Disease tags match recorded text mentions and require program-level verification.

Technology, programs & evidence

Founded in 2017; the company lists Suzhou headquarters, Rudong manufacturing and a Shanghai business office.

RNAa uses small activating RNA; saRNA here does not mean self-amplifying mRNA.

Program / serviceTarget / indicationRepresentative stageEvidence & scope
RAG-17SOD1 · SOD1-associated ALSPhase 1/2;2026-04-21Company announcement称II期给药中Investigational human study

Related news & literature

Company-name matches are discovery leads; verify entity identity and transaction roles in the original source.

No cataloged update explicitly mentions this company.

Same-field reading (not company-specific)
Vir Biotechnology / Business Wire

Vir schedules Phase 3 elebsiran–tobevibart results for The Liver Meeting

Vir Biotechnology announced that Phase 3 ECLIPSE 1 results for elebsiran plus tobevibart in chronic hepatitis delta will be presented on November 8, with an investor discussion on November 9. Elebsiran is an HBV-targeting siRNA; tobevibart is an antibody. The release announces the forthcoming readout and expanded Phase 2 presentations but does not disclose the Phase 3 numerical results.

Nitto Denko Avecia

Avecia and EnPlusOne agree to evaluate enzymatic RNA manufacturing

Nitto Denko Avecia and EnPlusOne signed an evaluation agreement for the ezRNA enzymatic synthesis platform. The phased program covers proof-of-concept studies, laboratory process evaluation, and technology transfer at Avecia facilities. The platform uses a water-based, template-free process. The agreement evaluates manufacturing feasibility; it does not announce a completed commercial manufacturing contract or a definitive platform license.

Integrated DNA Technologies

IDT and Aldevron launch research-grade base and prime editing RNA tools

IDT and Aldevron launched PE Ultra prime-editor mRNA, chemically modified pegRNAs, and six ABE8e-based editor mRNAs with a parallel screening kit. The companies also described guide-design support and stocked quantities from 20 micrograms to 1 milligram. These are research-use products; the announcement does not establish clinical safety, efficacy, or approval.

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Sources & open questions

  • Pipeline and dated release differ; registry status and clinical efficacy were not independently established. Logo and latest financing round remain unverified.
  1. Ractigen overview and locations ↗Ractigen Therapeutics · Undated
  2. Ractigen pipeline ↗Ractigen Therapeutics · Undated
  3. RAG-17 AAN company update ↗Ractigen Therapeutics · 2026-04-21

Inclusion is not endorsement or partner qualification. Assess company claims, clinical evidence, and project-specific capabilities separately.

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