Lead ProgramRBX-101 · NSCLC · STAT3
TechnologyGYM-siRNA Architecture · MERIT-Guided Design
TargetsSTAT3 · MYC · MDM2 · NF-κB
PipelineOncology · NSCLC · Sarcoma
Status● Discovery Stage · Active Programs
Modalityss-siRNA · TME-Responsive Nanoparticle
Lead ProgramRBX-101 · NSCLC · STAT3
TechnologyGYM-siRNA Architecture · MERIT-Guided Design
TargetsSTAT3 · MYC · MDM2 · NF-κB
PipelineOncology · NSCLC · Sarcoma
Status● Discovery Stage · Active Programs
Modalityss-siRNA · TME-Responsive Nanoparticle
NORA: Novel Onco RNAi Adventure

Rewriting the Rules of RNA Medicine SolRiNA™ GYM-siRNA Platform

A tumor microenvironment-responsive single-stranded RNA platform engineered to deliver tunable modulation of oncogenic transcription factors — designed for locoregional precision delivery where conventional therapies fail.

QSP
Systems Model
ss-siRNA
Single-strand
MERIT
Design Framework
Oncology Partnerships · Academic Collaborations · IP Portfolio
Platform Overview

SolRiNA™ in Action

A closer look at the GYM-siRNA platform — from structural design to locoregional delivery.

Explore Ribonabiologics Inc.

The SolRiNA™

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In-depth platform presentations, pipeline updates, and investor briefings — available exclusively to registered participants.

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SolRiNA™ Technology

The SolRiNA™ Platform

GYM-siRNA is engineered to deliver tunable modulation of oncogenic transcription factors —
combining structural RNA precision with tumor microenvironment-responsive delivery.

GYM-siRNA
Core Modality
5-Step
Pharmacological Cascade
TME-Gated
Conditional Activation
Network-Level
Pharmacodynamics

This page contains forward-looking statements regarding preclinical research programs. All platform descriptions reflect proprietary technology subject to pending patent protection. Programs have not received regulatory approval. For investigational use only.

Pharmacological Cascade

From RNA Exposure
to Sustained Target Suppression

Unlike conventional inhibitors that block a single molecular node, SolRiNA GYM-siRNA operates through a multi-stage pharmacological cascade. Each stage is modeled quantitatively, allowing prediction and optimization of downstream network responses.

The cascade bridges structural RNA engineering with network-level pharmacodynamics — translating a single RNA molecule into a network-level therapeutic effect.

01
Delivery
TME-Triggered Uptake
Acidic tumor microenvironment-responsive nanoparticles release payload selectively within the low-pH intratumoral environment
02
Loading
Argonaute Incorporation & RISC Assembly
Boltzmann-weighted conformational ensemble design engineered to optimize AGO2 loading efficiency; GYM architecture promotes strand selection
03
Silencing
Catalytic mRNA Cleavage
Sequence-specific target transcript degradation through Argonaute-2-mediated catalytic cleavage
04
Modulation
Transcription Factor Network Rebalancing
Attenuation of transcriptional activity — enabling tunable, non-binary suppression
05
Response
Sustained Transcription Factor Suppression
Progressive attenuation of oncogenic transcription factor activity — modeled by QSP-guided pharmacodynamic prediction

Ready to go deeper?

Explore the scientific foundation behind SolRiNA's network pharmacology approach.

Scientific Foundation

Modulating Oncogenic
Transcription Networks

Cancer is a network disease. SolRiNA is built on the principle that durable therapeutic responses require multi-node transcription factor modulation — not single-target inhibition.

GYM-siRNA
Core Molecule
MERIT
Design Framework
QSP
Modeling Framework
ACS
Compatibility Score

This page contains forward-looking statements regarding preclinical research programs. All platform descriptions reflect proprietary technology subject to pending patent protection. Programs have not received regulatory approval. For investigational use only.

Oncogenic Network Pharmacology

Why Tumors Are Resistant
to Single-Target Drugs

Oncogenic transcription networks exhibit complex regulatory dynamics — maintained by positive feedback and multi-node interactions — that allow them to sustain high-activity disease states resistant to single-agent intervention.

Conventional inhibitors that block a single node rarely achieve durable network-level responses. Tumor transcription factor networks adapt through compensatory rewiring, rendering monotherapy transiently effective at best. This is the fundamental problem the SolRiNA platform is designed to address.

By applying tunable RNA-mediated perturbations — calibrated through MERIT-based QSP modeling — the platform aims to produce sustained suppression of oncogenic transcription factor activity with durable pharmacodynamic effect.

Quantitative Systems Pharmacology

Modeling the Network,
Not Just the Target

The SolRiNA platform integrates RNA structural engineering with QSP modeling to predict and optimize therapeutic response at the molecular and network level. Models describe the full pharmacological cascade — from intracellular RNA exposure and RISC formation to transcription factor modulation and downstream gene silencing.

This computational layer enables rational dose regimen design, prediction of pharmacodynamic response profiles, and system-level simulation of how RNA perturbations propagate through oncogenic transcription factor networks over time.

Boltzmann-weighted conformational ensemble analysis identifies structurally optimal RNA candidates — enabling rational, ACS-guided selection and ranking of therapeutic sequences prior to experimental synthesis.

RNA Kinetics
Intracellular RNA exposure dynamics, RISC loading rates, catalytic turnover modeling
Network Dynamics
Nonlinear network modeling, feedback loop architecture, bifurcation analysis
PK/PD Integration
Dose-response prediction, temporal response profiles, PD modeling
Biomarker Linkage
TF activity as pharmacodynamic endpoint, translational biomarker correlation
Boltzmann Design
Boltzmann-weighted conformational ensemble approach to RNA structure optimization for AGO2 loading efficiency
Network Targeting
Multi-node transcription factor targeting enables adaptive, noise-resistant pharmacodynamic control

See the Pipeline

Explore how SolRiNA's scientific foundation translates into active therapeutic programs.

Therapeutic Pipeline

Targeting Convergent
Regulatory Nodes

active programs applying SolRiNA GYM-siRNA to oncogenic transcription circuits across cancer.

RBX-101
Lead: NSCLC
STAT3
Lead Target

This page contains forward-looking statements regarding preclinical research programs. All platform descriptions reflect proprietary technology subject to pending patent protection. Programs have not received regulatory approval. For investigational use only.

Program Overview

Programs

ProgramTarget CircuitIndicationModalityDiscoveryPreclinicalIND
RBX-101
Central NSCLC
STAT3Non-small cell lung cancerGYM-siRNA
RBX-201
MDM2-Amp Sarcoma
MDM2 · p53 PathwayDDLPS / Soft tissue sarcomaGYM-siRNA
Indication Rationale

Precision RNAi Oncology

RBX-101
Non-Small Cell Lung Cancer (NSCLC)
STAT3 hyperactivation drives tumor cell survival and immune evasion in NSCLC. High unmet need in centrally-located disease where systemic delivery is limited.
RBX-201
MDM2-Amplified Sarcoma (DDLPS)
Dedifferentiated liposarcoma is driven by MDM2 amplification suppressing p53 tumor suppressor function. Direct MDM2 knockdown via GYM-siRNA restores p53 pathway activity in a tumor type with no approved targeted therapy.
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IR Announcements

Latest Announcements

April 5, 2026 Press Release

Ribonabiologics Inc. Debuts with Next-Generation RNA Interference Platform Technologies

Siheung, S. Korea, April 5, 2026 — Ribonabiologics Inc. today announced its official launch, establishing a strategic focus on the development of next-generation RNA interference (RNAi) therapeutics.

Headquartered in Siheung, South Korea, Ribonabiologics is built on a foundation of advanced RNA engineering and structure-guided design. The company is developing its proprietary SolRiNA™ and GYM-siRNA™ platforms, designed to enhance Argonaute (RISC) loading efficiency and improve intracellular delivery — two of the most critical challenges in RNA therapeutics.

Ribonabiologics' lead programs are focused on solid tumor indications, with an initial emphasis on intratumoral delivery approaches. The company's integrated platform combines computational modeling with precision molecular design to optimize therapeutic performance and safety profiles.

Ribonabiologics is currently advancing its discovery pipeline and is actively seeking strategic partnerships to expand the application of its platform technologies globally.

Siheung, Republic of Korea IR Inquiry →
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