Targeted Drug Delivery
AtoCap overcomes the core limitation of low intracellular payload delivery through a technology that enables high local and intracellular drug concentrations and effective entry past cellular barriers.
~90% of drug delivery fails due to inadequate tissue and intracellular penetration now recognised as a major root cause of treatment failure, resistance, and relapse.
Most drugs never reach the true site of disease. They are blocked by biological barriers or absorbed by healthy tissue before acting on the target.
Despite decades of nanoparticle research, only ~0.7% of an injected dose reached target tissue in peer-reviewed analysis, leaving >99% in systemic circulation.
Wilhelm et al., Nature Reviews Materials, 2016The targeted drug delivery market is projected to reach ~$25B by 2030 at a ~16% CAGR, driven by pharma's recognition that delivery is the next frontier.
Pharma recognises that the challenge is no longer discovering molecules but delivering them where they act. Pfizer's $43B Seagen acquisition signals precision delivery is now a strategic imperative.
AtoCap's patented electrohydrodynamic (EHD) encapsulation creates biodegradable microcapsules that protect the drug in transit and release it at high concentration directly at the site of disease.
Our microporous capsules enable a high dose of the drug to penetrate biological barriers, delivering therapeutic concentrations directly at the site of infection.
The capsule surface is engineered to enable drug delivery through biofilms and intracellular reservoirs, reaching sites that conventional antibiotics cannot access.
Localised release minimises systemic exposure, reducing side effects and protecting against the accelerating crisis of antimicrobial resistance.
AtoCap's proprietary process uses precisely controlled electric fields to generate uniform, biodegradable microcapsules. Unlike conventional particle manufacturing methods, EHD encapsulation achieves:
AtoCap's encapsulation technology is designed to create value across multiple therapeutic areas, by enhancing treatment performance in fields such as oncology and hard-to-treat infections. Our lead program focuses on recurrent urinary tract infections (rUTIs), a highly prevalent condition that strains healthcare systems and, most importantly, profoundly affects the lives of patients living with chronic illness.
CapFuran reformulates nitrofurantoin into a targeted, intravesical therapy delivering antibiotic directly into bladder cells and biofilms where oral antibiotics cannot reach.
Urinary tract infections affect over 400 million people every year. For millions, what begins as a routine infection becomes a chronic, untreatable condition.
"I was diagnosed with a UTI in 2016. Nine years later, after being treated with 11 different antibiotics, I still have the same infection. I cannot work. I cannot travel. Every single facet of my life I once took for granted has been taken away." Patient living with recurrent UTIs
Behind every prescription are urologists and GPs doing their best, knowing that each new course of antibiotics carries its own cost and declining odds of success.
Current UTI therapies including antibiotics and vaccines fail to penetrate sufficiently into the bladder wall to kill bacteria embedded inside cells or producing a biofilm.
Symptoms may temporarily subside, but the infection persists. Embedded bacteria survive, later multiply, and produce the same cycle of relapse. The patient appears symptom-free, but the infection is never truly resolved.
Each failed course increases resistance risk and leaves the patient more vulnerable than before.
| Therapy | Limitation | Result |
|---|---|---|
| Oral Antibiotics | Reaches free bacteria only | Relapse |
| IV Treatments | Poor tissue penetration | Resistance |
| Vaccines | Do not eliminate intracellular reservoirs | Inconsistent |
| CapFuran | Reaches biofilms & intracellular reservoirs | >90% Reduction |
% bacterial reduction vs. placebo — human bladder organoid model
CapFuran® substantially improves bacterial killing vs. other treatments. Source: Lau W, Rohn J et al. Journal of Controlled Release, 2020. Human bladder organoid model.
CAPTURE is designed to generate decision-grade safety data and early efficacy signals unlocking early partnering discussions and a clear path into registration-enabling development.
Recurrent UTIs profoundly affect quality of life. These testimonies reflect the lived experience of patients for whom current treatments have not been enough.
A multidisciplinary team translating pioneering science into clinical application, combining deep academic expertise, industry experience, and strategic vision.

World-leading expert in drug delivery systems engineering. Designer of AtoCap's core EHD technology.

Leads the translational science driving CapFuran's development, with deep expertise in bladder biology and recurrent UTI pathology.

Driving company strategy across portfolio, business development and funding, alongside operational execution, grounded in deep pharmaceutical commercial expertise.

Strategic and commercial leadership with experience building and scaling impact-driven life science ventures.

Expert in university technology commercialisation and IP strategy, overseeing AtoCap's licensing and spinout development.

Brings investor perspective and strategic guidance as AtoCap advances toward clinical translation and Series A financing.
AtoCap is initiating a Series A round to fund CAPTURE, our Phase I/IIa first-in-human study. With strong preclinical data, GMP manufacturing established, and MHRA alignment confirmed, we are at the threshold of clinical validation.
This stage represents a favourable risk-adjusted entry point, with core biological, technical, manufacturing and regulatory uncertainties reduced and the company poised for a major value-defining milestone.
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