Accum™ Technology’s proprietary and patented drug delivery platform has 10x the impact on infected cells over other approved solutions.


Focused on broadly improving the therapeutic window of current ADCs based on existing technology.

Aiming for positive outcomes to possibly address cancer cell resistance issues observed previously in the clinic. 

With 100% ownership of findings and outcomes, this platform will fuel all  our future treatment discoveries including our prioritized Cancer Therapeutics and Vaccine Developments.


  • Accum™ Technology is the first-of-its-kind solution solving previous cancer treatment challenges.
  • Our proprietary and US patented tech-platform Accum™, has now solved these problems, and is the first-of-its-kind solution to accomplish a major and relevant milestone.

Accum™ has now proven its’ ability to deliver drugs – to the infected parts of infected cells only – at 10x the rate of current (ADC) solutions by:

  1. Accumulating more ADC’s into a target cell
  2. Breaking the cell membrane
  3. Successfully reaching the intercellular target site
  4. Delivering more of the intended drugs to the intended sites (only)

What does this mean?


Accum™ is a now a scalable global solution 


Accum™ is the most effective partner for current and future drug treatments – for cancer and other infectious diseases.

Watch here to see how it works:

This next-generation platform technology can be leveraged with other approved ADC drugs, while also driving in-house innovations for proprietary vaccines.  

Our process of getting here has involved three steps:

    1. We aimed to solve the problem of ineffective drug delivery
    2. We successfully targeted the nucleus (through Accum™)
    3. We targeted ADC’s and have been successful in delivering drugs to isolated cells. 

    Turning ADC challenges into proven platform solutions

    ACCUM™ Talk-Worthy Results:

    Overcoming problematic cell recycling and rejection patterns, ACCUM™ is the first solution to enable ADCs to control intracellular delivery of chemotherapeutic drugs, resulting in superior preclinical anti-tumor activity.

    By increasing the tumor targeting specificity – due to increased drug accumulation – non-specific toxicity in healthy cells is greatly reduced. 

    RESULT: We have increased intracellular accumulation of delivered drugs by 10x compared to current ADCs.


    ACCUM™ Innovative Approach

    1. Antibody retains tumor cells specificity
    2. Accum enables ADC to escape endosome entrapment
    3. Accum enables ADCs to be transported to the nucleus
    4. The drug is cleaved and release inside the nucleus
    5. Nucleus becomes a reservoir for the drug
    6. The reprogramed delivery system overcomes important resistant mechanisms relevant to ADC effectiveness.

    Highlights & Next Steps

    Completed pilots have proven Accum™ to be very stable, enabling higher drug retention, killing the infectious cell line by +2000x over comparable (approved) ADC, “T-DM1”.

    Recent mice trials have proven the ability of Accum™ to improve results.

    Validating Accum™ as a broad ADC platform technology 

    Building on these recent preclinical results, Dr. Jeffrey Leyton is also leading two additional discovery efforts: 

    • Develop single indication Accum™ modified ADC’s for cancers with unmet needs.
    • Developing Accum™ to enable antibodies to drug ‘undruggable’ targets

    Potential Market Growth

    With positive results, conjugation of Accum could be an important strategy to address cancer cell resistance issues observed in clinical studies.