KOP Therapeutics is seeking strategic partners and investors to advance its knockdown oncology platform toward IND-enabling development and clinical proof-of-concept. Biostatistician-confirmed preclinical results. Modular pipeline. Capital-efficient architecture.
95%
Peak Knockdown
Next-gen sequences, preclinical
Confirmed
Tumor Growth Inhibition
Charles River · p=0.049
4
Pipeline Programs
Prostate · Breast · Brain · Ovarian
0
Observed Toxicity
In preclinical in vivo work
KOP Therapeutics is developing a differentiated precision-oncology platform designed to deliver gene-silencing therapeutics directly to cancer cells. By combining targeted delivery, modular payload flexibility, a favourable early safety profile, and a scalable development strategy, KOP aims to unlock the therapeutic potential of RNA-based medicines across multiple cancer indications.
KOP's proprietary platform combines a tumour-targeting peptide with therapeutic oligonucleotides designed to silence cancer-driving genes directly within tumour cells. The platform has demonstrated strong gene knockdown and anti-tumour activity across multiple cancer cell lines, supporting its potential to address validated oncology targets with precision.
KOP's tumour-directed approach is designed to concentrate therapeutic activity within cancer cells while minimizing exposure to healthy tissue. Early preclinical studies have demonstrated anti-tumour activity without observed systemic toxicity, supporting the potential for an improved therapeutic window compared with less-targeted treatment approaches.
KOP is building a modular, plug-and-play delivery platform capable of supporting multiple nucleic-acid payloads, including antisense oligonucleotides, siRNA, mRNA therapeutics and potentially gene-editing technologies. This flexibility creates opportunities to generate multiple therapeutic candidates, expand across cancer indications and establish strategic partnerships around a common delivery engine.
KOP's technology is supported by a growing body of scientific and preclinical evidence, including tumour-targeting confirmation, gene knockdown, cancer-cell killing and in-vivo anti-tumour activity. Ongoing third-party studies, human-tissue testing and collaborations with recognized research and development partners are designed to further validate the platform and advance lead candidates toward clinical development.
Completed
In Vitro Validation
Up to 95% knockdown · 95 constructs screened · 4 cancer types
Completed
In Vivo PoC (Charles River)
Statistically significant TGI · p=0.049 · PC3 xenograft · no observed toxicity
Next Milestone
96-hr Kill Study
ED50 / ED90 · Galenvs Sciences CRO · Montreal, QC
Target
IND-Enabling Studies
GLP tox · CMC · FDA pre-IND meeting
96-hr Kill Study (ED50/ED90)
30%Galenvs Sciences CRO — next immediate milestone
Lead Optimization
25%Next-gen sequence advancement and construct refinement
IND-Enabling Studies
30%GLP toxicology, CMC, regulatory preparation
Operations & IP
15%Patent prosecution, team, and corporate development
INVESTOR INQUIRIES
We welcome discussions with institutional investors, family offices, strategic pharma/biotech partners, and accredited investors. Our corporate development team responds within one business day.
PHONE
604.771.8332