Proarrhythmia liability assessment and the comprehensive in vitro Proarrhythmia Assay (CiPA): An industry survey on current practice

• Published in: Journal of pharmacological and toxicological methods 2017-07, Vol.86, p.34-43
• Main Authors: Authier, Simon, Pugsley, Michael K., Koerner, John E., Fermini, Bernard, Redfern, William S., Valentin, Jean-Pierre, Vargas, Hugo M., Leishman, Derek J., Correll, Krystle, Curtis, Michael J.
• Format: Article
• Language: English
• Subjects: Animals; Arrhythmias, Cardiac - chemically induced; Calcium Channel Blockers - pharmacology; Computer Simulation; Drug Industry; Electrocardiography - drug effects; Humans; Induced Pluripotent Stem Cells; Ion Channels; Long QT Syndrome - chemically induced; Myocytes, Cardiac - drug effects; Sodium Channel Blockers - pharmacology; Surveys and Questionnaires; Telemetry
• ISSN: 1056-8719; 1873-488X
• DOI: 10.1016/j.vascn.2017.02.021

The Safety Pharmacology Society (SPS) has conducted a survey of its membership to identify industry practices related to testing considered in the Comprehensive In vitro Proarrhythmia Assay (CiPA). Survey topics included nonclinical approaches to address proarrhythmia issues, conduct of in silico studies, in vitro ion channel testing methods used, drugs used as positive controls during the conduct of cardiac ion channel studies, types of arrhythmias observed in non-clinical studies and use of the anticipated CiPA ion channel assay. In silico studies were used to evaluate effects on ventricular action potentials by only 15% of responders. In vitro assays were used mostly to assess QT prolongation (95%), cardiac Ca2+ and Na+ channel blockade (82%) and QT shortening or QRS prolongation (53%). For de-risking of candidate drugs for proarrhythmia, those assays most relevant to CiPA including cell lines stably expressing ion channels used to determine potency of drug block were most frequently used (89%) and human stem cell-derived or induced pluripotent stem cell cardiomyocytes (46%). Those in vivo assays related to general proarrhythmia derisking include ECG recording using implanted telemetry technology (88%), jacketed external telemetry (62%) and anesthetized animal models (53%). While the CiPA initiative was supported by 92% of responders, there may be some disconnect between current practice and future expectations, as explained. Proarrhythmia liability assessment in drug development presently includes study types consistent with CiPA. It is anticipated that CiPA will develop into a workable solution to the concern that proarrhythmia liability testing remains suboptimal.