Your browser doesn't support javascript.
loading
Long-term electrocardiographic safety monitoring in clinical drug development: A report from the Cardiac Safety Research Consortium.
Piccini, Jonathan P; Clark, Richard L; Kowey, Peter R; Mittal, Suneet; Dunnmon, Preston; Stockbridge, Norman; Reiffel, James A; Turakhia, Mintu P; Ziegler, Paul D; Kleiman, Robert B; Ismat, Fraz; Sager, Philip.
Afiliación
  • Piccini JP; Duke University Medical Center & Duke Clinical Research Institute, Durham, NC. Electronic address: jonathan.piccini@duke.edu.
  • Clark RL; Medtronic Diagnostics and Monitoring Research, Mounds View, MN.
  • Kowey PR; Lankenau Heart Institute and Jefferson Medical College, Philadelphia, PA.
  • Mittal S; The Valley Health System, Ridgewood, NJ.
  • Dunnmon P; Division of Cardiovascular and Renal Products, US Food and Drug Administration.
  • Stockbridge N; Division of Cardiovascular and Renal Products, US Food and Drug Administration.
  • Reiffel JA; Division of Cardiology, Columbia University, Medical Center, New York, NY.
  • Turakhia MP; VA Palo Alto Health Care System and Stanford University, Palo Alto, CA.
  • Ziegler PD; Medtronic Diagnostics and Monitoring Research, Mounds View, MN.
  • Kleiman RB; eResearch Technology, Inc. (ERT), Philadelphia, PA.
  • Ismat F; Bristol-Myers Squibb, Princeton, NJ.
  • Sager P; Stanford University, Stanford, CA.
Am Heart J ; 187: 156-169, 2017 May.
Article en En | MEDLINE | ID: mdl-28454799
ABSTRACT
This white paper, prepared by members of the Cardiac Safety Research Consortium (CSRC), discusses important issues regarding scientific and clinical aspects of long-term electrocardiographic safety monitoring during clinical drug development. To promote multistakeholder discussion of this topic, a Cardiac Safety Research Consortium-sponsored Think Tank was held on 2 December 2015 at the American College of Cardiology's Heart House in Washington, DC. The goal of the Think Tank was to explore how and under what circumstances new and evolving ambulatory monitoring technologies could be used to improve and streamline drug development. This paper provides a detailed summary of discussions at the Think Tank it does not represent regulatory guidance.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Monitoreo de Drogas / Evaluación de Medicamentos / Electrocardiografía Tipo de estudio: Guideline Límite: Humans Idioma: En Revista: Am Heart J Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Monitoreo de Drogas / Evaluación de Medicamentos / Electrocardiografía Tipo de estudio: Guideline Límite: Humans Idioma: En Revista: Am Heart J Año: 2017 Tipo del documento: Article