Targeted Therapy

YanHua Target

Precision-engineered exosome therapeutics for disease-specific intervention. Leveraging our targeted delivery platform to treat oncology, autoimmune, and rare diseases with unmatched specificity.

Precision Delivery to
Disease Sites

Our proprietary surface engineering platform equips exosomes with disease-specific targeting ligands, achieving precise tissue and cell-type selectivity.

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Active Targeting

Ligand-Receptor Mediated

Engineered surface ligands bind specifically to overexpressed receptors on diseased cells, achieving >90% targeting accuracy in validated models. Each indication uses a unique ligand cocktail optimized through high-throughput screening.

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Cargo Loading

Therapeutic Payload

Proprietary electroporation and incubation methods achieve high-efficiency loading of siRNA, mRNA, CRISPR components, or small molecule drugs with >80% encapsulation efficiency and preserved biological activity.

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Biodistribution

In Vivo Tracking

Near-infrared fluorescence and bioluminescence imaging confirm targeted accumulation at disease sites with minimal off-tissue distribution, typically achieving 15-25x enrichment at target vs. healthy tissue.

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Dose Optimization

PK/PD Modeling

Population pharmacokinetic modeling guides dose selection and treatment frequency, maximizing therapeutic index while minimizing potential adverse effects across diverse patient populations.

Clinical Development
Programs

YH-T01 — Solid Tumor Microenvironment Modulation

Targeted exosomes delivering immune checkpoint modulators to tumor-associated macrophages. IND-enabling studies completed. Phase I preparation underway.

Phase I ReadyOncology

YH-T02 — Autoimmune Disease Intervention

Exosomes engineered to deliver antigen-specific tolerance signals in rheumatoid arthritis and lupus models. Preclinical validation showing 70%+ disease activity reduction.

PreclinicalAutoimmune

YH-T03 — Neurodegenerative Disease

BBB-penetrant exosomes delivering neuroprotective cargo for Alzheimer's disease. Demonstrated 45% reduction in amyloid plaque burden in transgenic mouse models.

PreclinicalNeurology

YH-T04 — Rare Genetic Disorders

Gene-correcting exosomes for monogenic diseases. Proof of concept demonstrated in Duchenne muscular dystrophy cell models with restored dystrophin expression.

DiscoveryRare Disease
Clinical Partners

Partnered with Leading
Medical Institutions

Our clinical research network spans 9 top-tier hospitals across China, providing access to diverse patient populations and world-class clinical research infrastructure.

  • 9 Class-A tertiary hospitals in clinical network
  • Multi-center trial infrastructure established
  • IRB-approved protocols for investigator-initiated studies
  • Real-world evidence collection framework

Explore Clinical
Partnership Opportunities

Join us in advancing targeted exosome therapeutics from bench to bedside.

Partner With Us