Supporting the Future of Therapeutics: Novel Drug Modalities
At Axela Biosciences, we provide high-quality support for various drug modalities, including small molecules, antibodies/ADCs, peptides, protein degraders (PROTACs, molecular glues, etc.), cell therapy (CAR-T, CAR-NK), gene therapy (gene-editing), mRNA therapies, RNA interference (RNAi), and nanoparticle-based therapies, etc. Our deep expertise, highly sensitive assay platforms, and ready-to-use reagents enable smarter, faster, and more predictive preclinical and translational insights—accelerating your path from discovery to development.
Partial sample studies listed:
Antibody-Drug Conjugates (ADCs):
Internalization and trafficking studies
Target binding and specificity
Cytotoxicity and efficacy assays
Biomarker profiling and mechanism-of-action studies
Peptides:
Peptide stability in plasma, serum, and simulated GI fluids
Permeability and uptake studies across epithelial barriers
Receptor binding, signaling, and activity assays
Cell viability, apoptosis, and functional response readouts
In vivo-like potency and half-life prediction assays
Immunogenicity risk profiling
Targeted Protein Degraders (TPDs):
We provide tailored assay platforms for:
Screening degrader libraries
Monitoring target degradation kinetics
Evaluating selectivity and cellular context
Exploring downstream signaling and phenotypic outcomes
Cell Therapy:
Phenotypic characterization of immune and stem cell populations
Cytokine release profiling and immune activation assays
Cell viability, proliferation, and apoptosis analysis
Cytotoxicity and target cell killing assays (e.g., tumor cell lysis)
Transduction efficiency and expression verification
T cell exhaustion and memory marker profiling
Host immune response and cytokine storm risk assessment
Multiplex gene and protein expression analysis
In vitro potency assays aligned with intended MoA
Custom assay development tailored to specific cell products
Gene Therapy:
Directly profile 800 genes across 40 pathways Study processes known to impact gene therapy development and manufacturing • Cell State • Host-Vector Interactions • Innate Immune Response • Systemic Immunity • Toxicity