What We Do
Antibody Discovery
Our antibody drug discovery platforms, utilizing Ablexis’ AlivaMab® Mouse, are optimized for the discovery of therapeutic antibodies that move seamlessly into development. Accelerated timelines and reduced developability risks are achieved with naturally selected fully human variable domains, advanced antibody discovery workflows, integration of reliable, predictive screening cascades, and rapid identification of candidates that meet target product profile requirements.
AlivaMab Mouse
- Transgenic animal with a differentiated design for diversity, speed, developability, and freedom to operate
- Adopted by 12 of the top 25 global pharmaceutical companies
- Multiple AlivaMab antibodies have entered clinical trials, both as standard antibodies and as advanced therapeutic modalities
Immunizations
- Fit-for-target immunization strategies
- Breaking immune tolerance
- Strong, fast, molecularly diverse, high-affinity IgG responses
- Elicit antibodies that meet design goals, including for challenging targets such as GPCRs and other membrane multi-spanning targets
Fit-for-Purpose Screening
- Custom-designed screening cascades, including function-first cell-based assays
- Reliable, predictive high-throughput screens quickly identify the best candidates for progression
- Diversity and developability screens early in the process
- Processes scalable up to >105 cells for deep screening of the immune repertoire
Antibody Engineering
We have extensive experience in bispecific and CAR antibody engineering. We believe the best biologic drugs are selected from panels of antibodies with diverse sequences, broad epitope coverage, a range of affinities, and favorable biophysical properties. By coupling our discovery workflows with engineering pipelines, we ensure that high-quality antibody variable domains are employed. We leverage assay experience gained during discovery to rapidly evaluate engineered antibody activity.
Bispecific Engineering
- Diverse, clinically validated formats offer geometry and valency that mimic target geometry and drives desired biology
- Large lead matrices designed with productivity, product quality, activity, and stability in mind
- Robust functional assays identify leads with desired biological activity and de-risk potential off-mechanism liabilities
CAR Engineering for Cell-Based Therapies
- Evaluation of lead sequence and domain order to drive desired affinity while selecting high thermostability and avoiding self-interaction and polyreactivity/non-specific binding
- Cell-based reporter screening of lead sequences
- Ability to optimize hinge and linker composition
Reformatting
- Desired isotype, effector function, and half-life
Developability
- Stage-appropriate developability analysis incorporated throughout discovery and engineering of candidates to ensure the best molecules are carried forward