Laboratory assistant
Medical device
Medical device

ADCs

ADCs

Structurally Informed Liability Analysis

Structurally Informed Liability Analysis
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Identification of chemical liability sites (deamidation, oxidation, and isomerization), aggregation-prone patches, and problematic surface charges (positive, negative, and charge dipoles).

Identification of chemical liability sites (deamidation, oxidation, and isomerization), aggregation-prone patches, and problematic surface charges (positive, negative, and charge dipoles).

Payload Attachment Analysis

Payload Attachment Analysis

Quantitative analysis of ADC properties with different numbers of attached payloads (e.g. DAR) or different payload attachment sites, which exist in the drug product simultaneously.

Quantitative analysis of ADC properties with different numbers of attached payloads (e.g. DAR) or different payload attachment sites, which exist in the drug product simultaneously.

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Payload Property Analysis

Payload Property Analysis
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Surface properties of payloads and/or linkers (without attached protein) are analysed as if they were small molecule drugs.

For quantitative analysis, the properties of a payload of interest are either compared to our internal database of ADC payloads (shown), or our larger database of parenterally administered small molecule drugs.

Surface properties of payloads and/or linkers (without attached protein) are analysed as if they were small molecule drugs.

For quantitative analysis, the properties of a payload of interest are either compared to our internal database of ADC payloads (shown), or our larger database of parenterally administered small molecule drugs.

Quantitative Surface Property Analysis

Quantitative Surface Property Analysis

Over 90 structure- and sequence-derived properties are compared to our internal database. Our database contains the properties of over 900 therapeutic monoclonal antibodies (mAbs) that are already marketed or in clinical trials.

This analysis can be used to compare different linkers or payloads.

Over 90 structure- and sequence-derived properties are compared to our internal database. Our database contains the properties of over 900 therapeutic monoclonal antibodies (mAbs) that are already marketed or in clinical trials.

This analysis can be used to compare different linkers or payloads.

Uploaded

Expert Analysis

Expert Analysis

Data from liabilities, surface properties, and AI predictions are evaluated by our experienced scientists, in the context of the desired target product profile. Their deep expertise in formulation development ensures optimal interpretation of results and formulation strategy design.

Structurally Informed Liability AnalysisIdentification of chemical liability sites (deamidation, oxidation, and isomerization), aggregation-prone patches, and problematic surface charges (positive, negative, and charge dipoles).

Interested in how this can work for your molecule?

FAQ

Which molecule classes do you work with most often?
What is SMART Formulation® and how does it differ from classic screening?
How long does a typical formulation project take?
Can you supply non-GMP material for pre-clinical studies?

FAQ

Which molecule classes do you work with most often?
What is SMART Formulation® and how does it differ from classic screening?
How long does a typical formulation project take?
Can you supply non-GMP material for pre-clinical studies?

FAQ

Which molecule classes do you work with most often?
What is SMART Formulation® and how does it differ from classic screening?
How long does a typical formulation project take?
Can you supply non-GMP material for pre-clinical studies?