Chinese
Japan
English
Solving the AIDD validation bottleneck, closing the gap to pre-clinical development
Artificial intelligence is transforming antibody discovery, but success depends on more than generating large numbers of candidates. As AI increasingly produces molecules with novel and non-natural architectures, rapid validation and early developability assessment have become critical to identifying molecules with the optimal balance of functionality, manufacturability, and clinical potential.
At ProBio, we bridge this gap by combining over 20 years of antibody discovery expertise with integrated validation and developability strategies. Through customized screening cascades and our PrepCMC™ platform, we evaluate functional performance, biophysical properties, and CMC readiness in parallel, enabling earlier risk reduction, faster candidate selection, and accelerated progression to IND-enabling studies.
By incorporating CMC developability assessment during late discovery and advancing key development activities ahead of traditional timelines, ProBio helps clients identify the right candidate with greater confidence and achieve toxicology drug substance production in as little as 4.5 months, even for complex molecules and high-concentration formulations.
Smarter Screening for Better Candidates
Move beyond high-volume testing to rapidly identify molecules with the greatest chance of success.
Validation Backed By Real Drug Discovery Expertise
Identify true functionalleads early.
From Better Candidates to Faster IND Readiness
Optimize PCC selection with early CMC confidence.
The path between AI design and therapeutic reality
Integrated Platform
Fast & High-Throughput
AI-Ready Data
Proven Discovery Expertise
Years of deep expertise in biologics discovery
Projects in therapeutic antibody
Projects in the clinical phase and marketed
√ BVP/DNA/LPS/Insulin/KLH/Heprain ELISA
√ AC-SINS
√ DSF/DLS/iclEF
From transfection to Tox DS ready in as fast as 4.5 months
PrepCMC™ Fast Sample Preparation
PrepCMC™ Developability Study
ExpressCMC™ with PrepCMC™
Out of over 400 expressed bispecific constructs screened by FACS within three days, target A yielded 6 weak dual binders (n=176) and target B yielded 12 (n=193). In the nonspecific binding assay, 59 out of 336 hits registered below the BMK cutoff.
ProBio's integrated high-throughput screening platform enables rapid functional validation of large bispecific antibody libraries, helping AI-driven and conventional discovery programs quickly identify high-quality lead candidates. In this study, more than 400 expressed bispecific constructs were screened using a streamlined FACS-based workflow, progressing from antibody expression to data delivery within days.
The platform successfully identified target-specific dual binders against two antigens, while simultaneously assessing nonspecific binding liabilities to improve candidate quality. By combining automated expression, functional screening, and early developability assessment in a single workflow, ProBio helps clients reduce false positives, prioritize the most promising candidates earlier, and accelerate progression toward lead optimization and IND-enabling development.