Drug Tolerance in ADA Analysis

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Drug Tolerance in ADA Analysis Matthew Bentley www.eurofins.com

DRUG TOLERANCE What is Drug Interference and Why an issue in ADA analysis? Methodologies to overcome Drug Interference Acid Dissociation Affinity Capture Elution (ACE) Solid Phase Elution with Acid Dissociation (SPEAD) Case Studies Herceptin Avastin Summary

DRUG TOLERANCE The maximum amount of free drug in a study sample that allows detection of ADA at an acceptable sensitivity Why an issue? the presence of high drug levels in study samples can interfere with detection of ADA, especially in bridging assay formats Particularly relevant in multiple dose studies where drug concentrations may remain high for a significant period of the study Can interfere with PK and PD evaluations

DRUG TOLERANCE Compound Type MW (Kda) Test Method Drug Tolerance (µg/ml) Drug Tolerance (nm) Sensitivity (ng/ml Peptide ELISA 8.1 566 PEG-peptide RIPA 2.5 11 Peptide 3 RIPA 1.0 333 69 PEG-peptide ACE ECL 0.002 69 Fusion protein ECL 0.5 22 Fusion protein ACE ECL 0.46 94 Enzyme ECL 102 195 MAb 150 ACE elisa 500 3333 8 MAb 150 ECL 200 1333 63 PEG-peptide ECL 0.08 127 Peptide ECL 20 10

DRUG TOLERANCE Addressing Drug Tolerance First line approach often taken : Acid dissociation using Acetic Acid between 300 and 600mM

DRUG TOLERANCE One Size Does not fit all Optimisation Acid Concentration? Dissociation / Neutralisation Time? Temperature? Acid type e.g. Acetic, Glycine? Alternative formats ACE Acid Capture Elution: Several variations SPEAD Solid phase extraction with acid dissociation

Comparison of three assay formats Case Study: Anti-Avastin Three different formats developed for Avastin Bridging ECL with Acetic Acid Dissociation ACE SPEAD Early in development, the impact of added drug was evaluated on these formats Most promising format was to be chosen for further development 7

Bridging ECL format 1. Acid dissociate and neutralize 2. Incubate with biotin- and ruthenium-labeled drug 3. Capture on streptavidin ECL plate Ruthenium-labeled drug Sulfo- Tag H + OH - Free drug Anti-drug antibody B Biotinylated drug SA Streptavidin ECL Plate 8

ACE assay format (1) H + 1. Acid dissociate and neutralize 2. Capture on drug-coated plate OH - Free drug Anti-drug antibody 9

ACE assay format (2) 3. Elute using acid 4. Neutralize and coat on second plate 5. Detect with biotinylated drug and SA-HRP Streptavidin HRP HRP SA Biotinylated drug Anti-drug antibody H + OH - ECL Plate 10

SPEAD assay format (1) Free drug H + Anti-drug antibody 1. Acid dissociate and neutralize 2. Incubate with biotin-drug 3. Capture on streptavidin plate B Biotinylated drug B SA 11

SPEAD assay format (2) 4. Elute using acid 5. Neutralize and coat on ECL plate 6. Detect with ruthenylated drug Free drug Ruthenium-labeled drug Anti-drug antibody Sulfo- Tag Biotinylated drug H + SA Streptavidin Plate ECL Plate 12

Comparison of three assay formats Three different formats developed for Avastin Signal-to-noise ration (S/N) was used to compare methods. 15 or 150 µg/ml of unlabeled drug with an ADA level of 500 ng/ml (required sensitivity level) was examined All three formats had S/N close to 1.0 at 150 µg/ml drug = not tolerant to this level of drug Since bridging ECL assay had the highest S/N at 15 µg/ml drug, this was deemed the most promising format and chosen for further optimization 13

Comparison of three assay formats S/N at 500ng/mL ADA Method [Drug] (µg/ml) ACE SPEAD ECL 0 20.7 78.4 23.7 15 1.4 3.2 5.9 150 1 1.3 1.2 30 25 S/N (% of S/N without drug) 20 15 10 5 ACE SPEAD ECL 0 15 150 Drug added (ug/ml) 14

Optimization of ECL format 500 ng/ml of biotin- and ruthenium labeled drug gave best combination of sensitivity and drug tolerance 15

Optimization of ECL format After establishment of cut point, drug tolerance determined to be 150 µg/ml at 500 ng/ml ADA 16

CASE STUDY Case Study: Herceptin ADA - ACE Format comparison ACE selected Optimisation of Acid conditions Different concentrations and acids compared

HERCEPTIN ADA ACE Acids Compared: Acetic Acid (300 mm)! ph: 3.4 Acetic Acid (600 mm)! ph: 3.24 Glycine-HCl (100 mm)! ph: 3.02

HERCEPTIN ADA ACE 1 OD 0.1 0.3M Hac 0.6M Hac 0.1M Glycine cutpoint 0.01 0.1 1 10 100 1000 ug/ml trastuzumab 0.3M Acetic Acid 0.6M Acetic Acid 0.1M Clycine- HCl Drug Tolerance 9 µg/ml 30 µg/ml 150 µg/ml

Summary One size does not fit all Optimisation for method and compound of interest essential Method format: Conventional Acid dissociation ACE SPEAD ph, Concentration, Acid