Mabqi

LiteMab© Neo
Affinity Maturation

Seeking to turn your antibody candidates into more effective, safer and easier‑to‑develop assets?
  • Need to humanize your drug candidate?
  • Need to increase affinity of your binder at physiological pH?
  • Add additional characteristics to address other modalities or indications?
    • While maintain binding to the same epitope on the antigen, we can introduce additional species cross reactivty, internationalizing properties
  • Need to increase the therapeutic window of your binder / antibody
    • Preserve binding to the original epitope on the antigen
    • Reduce on-target / off-tumor toxicity in healthy tissues

How can we support the development of your next-generation biologics?

Benefit of Mabqi’s expertise in library design, extensive know-how in affinity and pH-sentivity maturation workflows to push your drug candidates toward higher potency, cleaner safety profiles, and better odds of regulatory and commercial success.

Based on your parental clone, different options are available (can be also combined )

  • LiteMab© Neo for Affinity maturation :
    • Increase binding strength
    • Sharpen specificity, reducing off‑target binding and improving both safety and therapeutic window.
    • De‑risk development by reducing the chance of late‑stage failures due to weak potency or poor target engagement.
  • LiteMab© Neo Sense for pH‑sensitivity maturation :
    • Optimize antigen binding in the tumor microenvironment environment (TME) while favoring weaker binding or even release in normal‑pH tissues to reduce on‑target off‑tissue toxicity.
    • Improve pharmacokinetics and tissue penetration, for example by enabling “pH‑dependent” recycling or release in endosomal compartments.
    • Enhance manufacturability and stability: understanding and controlling pH sensitivity helps formulation scientists design buffers that minimize degradation, aggregation, and loss of activity over shelf life.

How does it work?

  • Program based on your parental clone (discovery, preclinical, clinical stages or on the market)
  • Design of a customized library based on the parental sequenceDiversity is introduced at selected and variablepositions and destabilizing positions are avoided.
  • AI-powered dual display platform
  • Functionality-driven discovery workflow
  • Comprehensive characterization and functional validation of the binders

Expand your pipeline with next-gen drug candidates!

Curious to explore your challenges with a specialized discovery partner? 
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