Anti-drug Antibody Magnitude and Clinical Relevance Using Signal to Noise (S/N): Bococizumab Case Study

AAPS J. 2023 Sep 2;25(5):85. doi: 10.1208/s12248-023-00846-x.

Abstract

Historically, the biopharmaceutical industry has used titer to characterize the magnitude of an anti-drug antibody (ADA) response. While reporting levels of antibodies in terms of titer is generally understood and accepted by regulatory and medical communities, titer values are inherently variable given the multiple serial dilutions and reporting a value either directly before or interpolated at the assay cut point on the lower plateau of the assay curve range. Using S/N is an appealing alternative approach to titer as it simplifies analysis with less dilutions, significantly reducing testing, time, and resources and provides a more precise value potentially differentiating low-level ADA responses. Current bridging electrochemiluminescence (ECL) ADA assays using Meso Scale Discovery (MSD) platform are also significantly more sensitive and drug tolerant with wider assay ranges compared to historic ELISA platforms; therefore, ADA response based on S/N may help differentiate and identify those ADA samples that are more likely to be clinically relevant. Bococizumab is a humanized monoclonal antibody targeting proprotein convertase subtilisin-kexin type 9 (PCSK9), which reduces plasma levels of low-density lipoprotein (LDL) cholesterol. Bococizumab was discontinued during Phase 3 clinical development based in part on the high rate of ADA and wide variation in LDL cholesterol responses among patients. The impact of anti-bococizumab antibodies on pharmacokinetic (PK) and pharmacodynamic (PD) endpoints was originally assessed using titer. Retrospective analysis of anti-bococizumab ADA responses using S/N ratios illustrates that S/N is an acceptable alternative to titer for characterizing the magnitude of ADA response and interpretation of clinically relevant ADA.

Trial registration: ClinicalTrials.gov NCT01968954 NCT01968967 NCT01968980 NCT02100514.

Keywords: anti-drug antibodies (ADA); clinical relevance; immunogenicity; signal-to-noise ratio (S/N); titer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Clinical Relevance*
  • Enzyme-Linked Immunosorbent Assay
  • Humans
  • Proprotein Convertase 9*
  • Retrospective Studies

Substances

  • PCSK9 protein, human
  • Proprotein Convertase 9

Associated data

  • ClinicalTrials.gov/NCT01968954
  • ClinicalTrials.gov/NCT01968967
  • ClinicalTrials.gov/NCT01968980
  • ClinicalTrials.gov/NCT02100514