Precision Gene-Silencing Therapeutics

Silencing the source
of lipid disease

A first-in-class RNA therapy targeting the liver to simultaneously address fatty liver disease and cardiovascular lipid risk, with a single injection every 3 to 6 months.

Lead selection complete  ·  2026
IND enabling  ·  mid 2026 – 2027
Phase 2a PoC  ·  anticipated 2030–2031
Belgium  ·  Founded 2025
~1.54B
Adults affected globally by cardiometabolic disease
$115B
Cardiometabolic treatment market, 2025
$36B+
M&A in cardiometabolic in 2025 alone
The Lipid Problem

A convergent cardiometabolic epidemic

Most MASLD/MASH patients don't have "just liver disease." They carry cardiometabolic risk that kills first.

Dyslipidemia, T2D, MASLD and MASH share the same upstream drivers: caloric excess, insulin resistance, adipose dysfunction, and chronic inflammation. The result is a single connected epidemic affecting 1.54 billion adults.
MASLD affects ~38% of the global population, with a meaningful subset progressing to MASH and fibrosis.
Cardiovascular disease is the #1 cause of death globally. Dyslipidemia amplifies both ASCVD risk and MASLD/MASH progression.
70% of T2D patients have fatty liver. 80%+ of patients with MASH have obesity. These conditions are biologically inseparable.
Younossi et al. 2025; Betlejewska et al. 2025
The metabolic cascade
Competitive Positioning

The only therapy with full dual benefit

Existing therapies treat one axis. SIG-001 is the only approach designed to simultaneously address MASLD/MASH and atherogenic dyslipidemia.

Liver / MASH benefit ↑
Liver-focused / limited CV
FGF21
THRβ (P3)
Full dual benefit
SIG-001
Limited benefit
GLP-1 (M)
CV-focused / limited liver
Statins (M)
PCSK9 inhib. (M)
ApoB-ASO (M)
← Low Cardiovascular / lipid benefit (ApoB, TG, LDL) High →
M = Marketed  |  P3 = Phase 3  |  Strong overlap: 70% of T2D patients have fatty liver. 80%+ of MASH patients have obesity. 2025 saw $36B+ in M&A concentrated in these two areas.
Mechanism of Action

Three synergistic pathways.
One injection.

1
Reduces hepatic lipid accumulation
Shifts hepatocytes from storing lipids to burning them via autophagy and beta-oxidation, directly addressing MASLD/MASH progression from fibrosis stage F1.
2
Cuts export of harmful lipids
Degrades ApoB100 before VLDL assembly. Fewer VLDL particles released, lower blood triglycerides, improved atherogenic lipid profile.
3
Supercharges lipid clearance
Activates the LPL pathway, accelerating the breakdown of triglyceride-rich lipoprotein particles and reducing atherogenic remnant cholesterol and cardiovascular risk.

SIG-001 uses GalNAc-conjugated siRNA, the same validated delivery platform as inclisiran and givosiran, to silence a novel liver-expressed gene with a central role in lipid metabolism.

01
Built on validated biology
SIG-001's target was identified in our scientific founder's laboratory, the same group that underpinned the development of landmark lipid-lowering medicines now on the multibillion pharma market.
02
De-risked delivery platform
GalNAc conjugation targets ASGPR on hepatocytes for selective liver delivery. Multiple approved drugs have established the safety, manufacturing, and regulatory pathway.
03
Human genetic validation
Hundreds of human homozygous loss-of-function individuals identified, all healthy, with demonstrated protection against MASH. This de-risks the target before the first patient is dosed.
Programs

Development pipeline

Pre-clinical work runs through mid-2026, followed by IND-enabling studies through 2027. Phase 1 is planned for 2028–2029, with Phase 2a proof-of-concept anticipated 2030–2031.

Program
Pre-Clinical
IND Enabling
Phase 1
Phase 2
SIG-001
Novel liver target · GalNAc-siRNA
Lead Program
2025 – mid 2026
mid 2026 – 2027
2028 – 2029
2030 – 2031
SIG-002
Undisclosed target
Discovery
In progress
TBD
TBD
TBD
Complete
Active
Planned
The Team

Built to execute

A multidisciplinary team combining industry, clinical, scientific, and financial expertise with direct ties to the biology underpinning SIG-001.

L. Matonog
Chief Executive Officer

Industry experience across Sanofi, AstraZeneca and early-stage start-ups, with consulting at PwC. R&D, CMC and regulatory strategy background spanning first-in-class cardiovascular drugs, fitusiran, mRNA therapeutics, and GalNAc-siRNA.

Undisclosed
Scientific Founder

Internationally recognised authority on a therapeutically relevant enzyme family, the same group that underpinned the development of landmark lipid-lowering medicines now on the multibillion pharma market. 800+ peer-reviewed publications and major national scientific honours.

D. Côté-Vaillancourt
Chief Financial Officer

Previous roles as Chief of Staff, CFO, CTO and Head of M&A following his career at McKinsey. Proven track record in capital allocation and strategic transactions.

Mark V.S.
Chief Operating Officer

20+ years of operational leadership across 250+ client sites. Program management and operational excellence in complex multi-site R&D organisations.

Scientific Team

Our in-house scientific team brings hands-on experience in metabolic disease and immuno-oncology from leading European biotech, currently advancing SIG-001 through lead selection.

Julie Chesné
Principal Scientist  ·  Ex-iTeos, Metabolic & IO
Thibaut Janss
Senior Scientist  ·  Ex-iTeos, Metabolic & IO
Scientific Advisors

SIG-001 is supported by world-class scientific expertise across enzyme biology, hepatology, and RNA therapeutics.

Prof. E. Sokal
Hepatology Advisor
Hepatologist and ex-CEO of Promethera and Cellaion. Clinical expert in liver diseases with extensive CMO and medical advisory experience across clinical-stage biotech.
Undisclosed
RNA & Oligo Specialist
Expert in functional genomics and oligonucleotide translation, with a Harvard RNA Institute Fellowship. Brings direct GalNAc-siRNA platform expertise to SIG-001's development.
Strategic & Business Advisors

Silengenics is building a board of strategic and business advisors spanning biotech investment, regulatory affairs, and commercial development. Full advisory board announcement forthcoming.

Investors

Investor materials

Access our full product overview including pipeline, mechanism of action, market opportunity, and financing plan. Available to qualified investors upon request.

Company & Investment Overview
Pre-clinical stage, lead program, IP, headquarters and inception details.
Pipeline & Development Plan
SIG-001 roadmap, milestones, regulatory strategy and Phase 1/2 design.
Market & Financing
TAM/SAM/SOM analysis, use of proceeds and financing requirements 2026–2030.
View Product Overview

Password-protected. Available to qualified and accredited investors only.

Contact

Partner with Silengenics

We are engaging with qualified investors, clinical collaborators, and potential strategic partners as we advance SIG-001 toward the clinic.

General Enquiries
Headquarters
Belgium