Increased tumor retention needed for maximum therapeutic impact
Founding Team
Askar Kuchumov, Ph.D.
15 years of hands-on entrepreneurial experience building innovative drug development companies starting as a VC investor.
Co-founder of several startups in oncology, having taken two programs from discovery stage to Phase II clinical.
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Morten Meldal, Ph.D.
2022 Nobel Laureate in Chemistry
Co-inventor of click chemistry’s copper-catalyzed azide–alkyne cycloaddition (CuAAC), a reaction that reshaped bioconjugation, diagnostics, and drug discovery.
He is a Professor at the University of Copenhagen, Denmark, and a pioneer of modern combinatorial and solid-phase peptide synthesis.
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A New Class in Tumor-Targeted Therapy
Solid tumor treatment has reached a turning point.
Antibody-drug conjugates have proven that precision targeting works — but their size limits how deeply they can penetrate tumors, and their complexity drives high cost and safety trade-offs.
Peptide-drug conjugates can go deeper, yet lose impact by washing out too quickly.
Our answer is Tumor-Anchored ConjugatesTM — a proprietary, fully synthetic conjugate platform designed from the ground up to overcome these barriers. TACs unite three critical capabilities in one construct: the precision of antibodies, the penetration of peptides, and engineered tumor retention that keeps potent payloads active where they matter most.
The Unsolved Challenges in Solid Tumor Drug Delivery
Antibody-Drug Conjugates (ADCs)
Clinically validated, but large size limits penetration into solid tumors; complex and costly to manufacture; long circulation time leads to increased off-target toxicities.
Peptide-Drug Conjugates (PDCs)
Excellent penetration but short tumor dwell time; payload clears too quickly to achieve full therapeutic effect.
Unmet Need
A delivery system with the precision of antibodies, the deep reach of peptides, and the anchoring power to stay in tumors long enough to maximize therapeutic impact - without antibody complexity.
Our Solution: Tumor-Anchored ConjugatesTM
TACs are built to rival ADCs in precision while surpassing them in penetration, safety, and scalability.
Engineered Anchoring Mechanism
Keeps the drug localized, increasing dwell time and therapeutic index.
High-affinity / High-avidity binding
to tumor-associated or tumor microenvironment markers ensures high tumor specificity and increased retention time.
Optional Conditional Activation
within the tumor microenvironment using validated approaches for better safety profile.
Built-in Dual Payload Delivery Mechanism
via target-dependent and target-independent pathways: broad range of targets / tumors / indications which can be accessed via TAC.
Why Now
ADC Market Momentum
$20B+ and growing; pharma is actively searching for alternatives with better penetration and lower cost.
Advances in Technology
AI/in silico cyclic peptide design now enables antibody-like affinity, enhanced stability with non-natural amino acids, and modular binders tailored to different tumor targets.
Demand for Safer, More Potent Platforms
Market pressure for higher therapeutic index, fewer side effects, and scalable and cost-effective manufacturing.
We are fundraising and building.
Let’s shape the future of tumor-targeted therapeutics - together.