Targeted Drug Delivery

Unlocking the Full Potential of Treatments Through 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.

The Efficacy Gap

~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.

~90%
of drug delivery fails

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.

<1%
of injected dose reaches target tissue

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, 2016
$25B
global market by 2030

The 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.

Why Conventional Treatments Fail

Biological Barriers

Cell membranes, biofilms and tissue layers block drugs from reaching intracellular infection sites.

Systemic Toxicity

Drugs distributed throughout the body expose healthy tissue to high concentrations, causing side effects.

Repeated Treatment Cycles

Insufficient penetration means infections persist, driving chronic relapse, escalating resistance, and rising healthcare costs.

Antimicrobial Resistance

Persistent sub-therapeutic exposure accelerates AMR, projected to cause up to 10 million deaths annually by 2050.

" Up to 80% of the targets we are seeking to reach are inside cells. AstraZeneca, 2024

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.

A Technology Platform Designed to
Overcome Biological Barriers

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.

Protect

Our microporous capsules enable a high dose of the drug to penetrate biological barriers, delivering therapeutic concentrations directly at the site of infection.

Deliver

The capsule surface is engineered to enable drug delivery through biofilms and intracellular reservoirs, reaching sites that conventional antibiotics cannot access.

Reduce

Localised release minimises systemic exposure, reducing side effects and protecting against the accelerating crisis of antimicrobial resistance.

EHD cone-jet process — AtoCap laboratory footage

Electrohydrodynamic (EHD) Encapsulation

AtoCap's proprietary process uses precisely controlled electric fields to generate uniform, biodegradable microcapsules. Unlike conventional particle manufacturing methods, EHD encapsulation achieves:

  • Ultra-high encapsulation efficiency to maximise drug loading
  • Tunable, uniform capsule size and structure
  • GMP-compliant and scaleable manufacturing (Bionanopharma partnership)
  • Versatile platform technology adaptable for multiple therapeutics
🔒
Patent-Protected Platform Exclusive worldwide licence from UCL Business. Granted process patents and pending filings for CapFuran.

A Technology Designed to Transform
Drug Delivery in High-Impact Diseases

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.

Lead Program
Recurrent UTI
CapFuran®
Phase I/IIa
Bladder Cancer
Encapsulated chemo
Preclinical
Key Genitourinary Infections
Platform extension
Discovery
Skin Infections
Platform extension
Discovery
Infected Joints
Platform extension
Discovery
Lead Program (Phase I/IIa)
Preclinical
Discovery
Bladder cells microscopy

AtoCap's Lead Program for
Recurrent Urinary Tract Infections

CapFuran reformulates nitrofurantoin into a targeted, intravesical therapy delivering antibiotic directly into bladder cells and biofilms where oral antibiotics cannot reach.

CapFuran biofilm penetration
CapFuran microparticles penetrating bladder biofilm

A Common Infection Turned Lifelong Struggle

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.

400M+
UTI cases annually worldwide
Women experience recurrence within 6 months
50%+
Pathogens resistant to first-line antibiotics
Infections per year for chronic sufferers

Existing Treatments Cannot Reach Embedded Infections

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
CapFuran substantially improves bacterial killing vs. other treatments

% bacterial reduction vs. placebo — human bladder organoid model

Placebo
0%
0%
Oral Nitrofurantoin Standard of care
38%
CapFuran® AtoCap lead program
>90%

CapFuran® substantially improves bacterial killing vs. other treatments. Source: Lau W, Rohn J et al. Journal of Controlled Release, 2020. Human bladder organoid model.

>90%
Bacterial reduction with CapFuran®
2.4×
More effective than standard oral antibiotics
No Observed Toxicity
CapFuran® demonstrated no cytotoxicity in human bladder organoid models at therapeutic doses.
Peer-Reviewed Publication
Journal of Controlled Release, 2020
Positive MHRA Engagement
Regulatory alignment confirmed. Advancing toward first-in-human study.
GMP Manufacturing Complete
Technology transfer with Bionanopharma (Insud Pharma Group), Spain

CAPTURE: Phase I/IIa First-in-Human Study

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.

IndicationRecurrent UTI (≥3/year or ≥2 in 6 months)
SiteUniversity College London Hospital (UCLH)
Design20 patients, 4 sequential cohorts
DosingIntravesical escalation 1 to 7 daily instillations
Primary EndpointSafety
Secondary EndpointsTolerability, microbiology and recurrence signals

CAPTURE Trial Timeline

2024–2026
Preclinical
GMP manufacturing, organoid efficacy data, MHRA alignment confirmed
2026 Q3
Site Activation
UCLH contracting, pharmacy & clinical facility readiness
Next Step
2027 Q3
First Patient Dosed
Sequential 4-patient cohort dosing begins
2028 Q3
Dosing Complete
All cohorts dosed. Early BD discussions enabled.
2029 Q3–Q4
CAPTURE Complete
Primary readout. Safety, tolerability & efficacy data. Partnering discussions unlocked.
2030 Q1–Q2
Phase IIb Initiation
Next-stage efficacy study commences

Voices From the Patient Community

Recurrent UTIs profoundly affect quality of life. These testimonies reflect the lived experience of patients for whom current treatments have not been enough.

Coming Soon

Scientific and Commercial
Leadership

A multidisciplinary team translating pioneering science into clinical application, combining deep academic expertise, industry experience, and strategic vision.

Prof Eleanor Stride

Prof Eleanor Stride

Founder & Non-Executive Director
Statutory Professor of Biomaterials
University of Oxford
OBE, FREng, FIET

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

Dr Jennifer Rohn

Prof Jennifer Rohn

Chief Scientific Officer
Head of Urological Biology
Division of Medicine, UCL

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

María José Baixauli

María José Baixauli

General Manager
Former Novartis and Johnson & Johnson
15+ years pharma leadership

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

Alex Pitt

Alex Pitt

Non-Executive Director
Founder, Mustardseed Impact

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

Dr Weng Sie Wong

Dr Weng Sie Wong

Non-Executive Director
Senior Business Manager, UCL Business

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

Cristina Diaz-Dickson

Cristina Diaz-Dickson

Non-Executive Director
Lead Investor

Brings investor perspective and strategic guidance as AtoCap advances toward clinical translation and Series A financing.

Join Us at a Strategic
Inflection Point

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.

Get in Touch

Investor enquiries, partnership discussions, and press contact.