Accelerating the In Vivo Revolution: Next-Generation CAR-T Preclinical Solutions

Your Integrated Partner, De-Risking the Journey from CAR Molecule Engineering to Clinical Translation.

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(Uscanga-Palomeque et al., 2023)

Redefining Cell Therapy: The Direct-to-Patient Revolution

In vivo CAR-T therapy is redefining the future of cell immunotherapy. Rather than engineering T cells outside the body, this breakthrough approach reprograms a patient’s immune cells in vivo using viral or non-viral vectors. The field is advancing rapidly, with multiple candidates entering clinical development and early data showing highly promising therapeutic efficacy across oncology and emerging autoimmune applications. This momentum is driving strong industry interest and significant investment.

As an off-the-shelf modality, in vivo CAR-T has the potential to overcome major limitations of traditional ex vivo manufacturing-high cost, complex logistics, and lengthy production cycles. However, unlocking its full potential still depends on solving key challenges, including achieving highly specific T-cell targeting and minimizing systemic toxicity caused by off-target biodistribution.

Integrated Preclinical Solutions for In Vivo CAR-T Therapy

Accelerate your journey from concept to IND with a unified preclinical partnership

  • CAR Molecule Engineering
  • Delivery System Development
  • In Vitro Delivery & Efficacy Screening
  • In Vivo Efficacy in Translational Models
  • Pharmacokinetics (PK) & Biodistribution (BD)
  • Safety Assessment

CAR Molecule Engineering

scFv/VHH Screening & Optimization

  • Hybridoma Discovery
  • Single B Cell Screening
  • Human Naïve Library Screening
  • Antibody Affinity Maturation
  • sdAb Immunized Library Screening
  • sdAb Naïve Library Screening
  • Antibody Humanization

Structural Optimization

  • Hinge Region Optimization
  • Transmembrane Domain Optimization
  • Intracellular Signaling Domain Optimization

Delivery System Development

Viral Vector Engineering

Lentiviral Envelope Engineering

  • VSV-G Replacement
  • VSV-G Point Mutation

Lentiviral Tropism Refinement

Lentiviral Safety Engineering

  • MHC Knockout
  • CD47 Overexpression

Lentiviral Vector Structure Optimization

  • Suicide Gene/Safety Switch
  • Regulated Expression Module (RACP)
  • T Cell-Specific Promoter

Non-Viral Delivery Engineering

Sequence Design & Vector Construction

  • Plasmid Construction
  • CAR mRNA Sequence Design & Optimization

LNP Formulation Screening

Targeting Optimization

  • Antibody Design & Optimization
  • Antibody-LNP Conjugation (Ab-LNP)

In Vitro Delivery & Efficacy Screening

  • Validated Target Cell Model Establishment
  • CAR Expression Kinetics & Stability
  • Vector Tropism & Transduction Specificity
  • Vector Screening & Cellular Compatibility
  • Functional Efficacy Evaluation

In Vivo Efficacy in Translational Models

Tumor Models

  • Cell Line-Derived Xenograft (CDX)
  • Syngeneic Mouse Models
  • Metastasis Models
  • Patient-Derived Xenograft (PDX)
  • Orthotopic Models
  • High Stromal Tumor Models

Other Disease Models

Humanized Mouse Models

  • Humanized PBMC Mouse Models
  • Target Humanized Transgenic Mouse Models
  • Humanized CD34+ HSC Mouse Models

Inflammation & Autoimmune Disease Models

  • Multiple Sclerosis (MS) Models
  • Systemic Lupus Erythematosus (SLE) Models

Pharmacokinetics (PK) & Biodistribution (BD)

  • CAR-T Cell Pharmacokinetics (PK)
  • CAR-T Cell Biodistribution (BD)
  • CAR Expression Kinetics & Quantification
  • Vector Pharmacokinetics (PK)
  • Vector Biodistribution (BD)

Safety Assessment

Immunotoxicity

  • Cytokine Release Syndrome (CRS) Assessment
  • Immune Effector Cell-Associated Neurotoxicity (ICANS) Assessment
  • Cytokine Profile Quantification
  • Immune Cell Subset Analysis

Immunogenicity

Vector & Genetic Safety

  • Genetic Integration Site Analysis
  • Insertional Mutation Risk Assessment
  • On-target/Off-target toxicity Assessment

General Toxicology

Why Partner with Us?

More than a CRO, we are your strategic R&D extension

End-to-End Preclinical Solutions

We provide fully integrated preclinical solutions for in vivo CAR-T therapies-from CAR design to vector engineering and in vitro/in vivo evaluation.

Custom Study Strategies

Our team designs flexible, tailored study strategies that adapt to evolving project needs, enabling rapid optimization and adaptive adjustments within our in vivo CAR‑T development platform.

Deep Therapeutic Expertise

Leverage our extensive experience in immuno-oncology and in vivo CAR-T therapy to navigate complex biology, optimize strategies, and advance programs efficiently.

Accelerated Translational Support

We streamline preclinical workflows to reduce turnaround time and support seamless progression from discovery to clinical translation.

Ready to Advance Your In Vivo CAR-T Program?

All inquiries receive a response from a senior scientist within 24 hours.

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