MetaTarget Therapeutics, Inc.
Redefining targeted solid tumor treatment

Synthetic conjugate platform integrating:
  • Accuracy of antibodies
  • Penetration of peptides
  • 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.
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