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Preclinical Safety Evaluation and Human Dosimetry of [18F]MK-6240, a Novel PET Tracer for Imaging Neurofibrillary Tangles.
Koole, Michel; Lohith, Talakad G; Valentine, John L; Bennacef, Idriss; Declercq, Ruben; Reynders, Tom; Riffel, Kerry; Celen, Sofie; Serdons, Kim; Bormans, Guy; Ferry-Martin, Sandrine; Laroque, Philippe; Walji, Abbas; Hostetler, Eric D; Briscoe, Richard J; de Hoon, Jan; Sur, Cyrille; Van Laere, Koen; Struyk, Arie.
Afiliação
  • Koole M; Division of Nuclear Medicine, Leuven University Hospitals and UZ Leuven, Leuven, Belgium.
  • Lohith TG; Translational Imaging Biomarkers, Merck & Co., Inc., 770 Sumneytown Pike, Mailstop WP44D-216, West Point, PA, 19486, USA. talakad.lohith@merck.com.
  • Valentine JL; Safety Assessment and Laboratory Animal Research, Merck & Co., Inc., West Point, PA, USA.
  • Bennacef I; Translational Imaging Biomarkers, Merck & Co., Inc., 770 Sumneytown Pike, Mailstop WP44D-216, West Point, PA, 19486, USA.
  • Declercq R; Translational Pharmacology Europe, Merck Sharp & Dohme Inc., Brussels, Belgium.
  • Reynders T; Translational Pharmacology Europe, Merck Sharp & Dohme Inc., Brussels, Belgium.
  • Riffel K; Translational Imaging Biomarkers, Merck & Co., Inc., 770 Sumneytown Pike, Mailstop WP44D-216, West Point, PA, 19486, USA.
  • Celen S; Radiopharmaceutical Research, KU Leuven, Leuven, Belgium.
  • Serdons K; Division of Nuclear Medicine, Leuven University Hospitals and UZ Leuven, Leuven, Belgium.
  • Bormans G; Radiopharmaceutical Research, KU Leuven, Leuven, Belgium.
  • Ferry-Martin S; Safety Assessment and Laboratory Animal Research, Merck Sharp & Dohme, Riom, France.
  • Laroque P; Safety Assessment and Laboratory Animal Research, Merck Sharp & Dohme, Riom, France.
  • Walji A; Discovery Chemistry, Merck & Co., Inc., West Point, PA, USA.
  • Hostetler ED; Translational Imaging Biomarkers, Merck & Co., Inc., 770 Sumneytown Pike, Mailstop WP44D-216, West Point, PA, 19486, USA.
  • Briscoe RJ; Safety Assessment and Laboratory Animal Research, Merck & Co., Inc., West Point, PA, USA.
  • de Hoon J; Center for Clinical Pharmacology, University Hospitals of Leuven, Leuven, Belgium.
  • Sur C; Translational Imaging Biomarkers, Merck & Co., Inc., 770 Sumneytown Pike, Mailstop WP44D-216, West Point, PA, 19486, USA.
  • Van Laere K; Division of Nuclear Medicine, Leuven University Hospitals and UZ Leuven, Leuven, Belgium.
  • Struyk A; Translational Pharmacology, Merck & Co., Inc., North Wales, PA, USA.
Mol Imaging Biol ; 22(1): 173-180, 2020 02.
Article em En | MEDLINE | ID: mdl-31111397
ABSTRACT

PURPOSE:

[18F]MK-6240 is a selective, high-affinity positron emission tomography tracer for imaging neurofibrillary tangles, a key pathological signature that correlates with cognitive decline in Alzheimer disease. This report provides safety information from preclinical toxicology studies and first-in-human whole-body biodistribution and dosimetry studies of [18F]MK-6240 for its potential application in human brain imaging studies. PROCEDURES MK-6240 was administered intravenously (IV) in a 7-day rat toxicity study at × 50, × 100, and × 1000 dose margins relative to projected highest clinical dose of 0.333 µg/kg. The IV formulation of MK-6240 for clinical use and the formulation used in the 7-day rat toxicity study was tested for hemolysis potential in human and Wistar rat whole blood. Sequential whole-body positron emission tomography scans were performed in three healthy young subjects after IV bolus injection of 180 ± 0.3 MBq [18F]MK-6240 to characterize organ biodistribution and estimate whole-body radiation exposure (effective dose).

RESULTS:

MK-6240 administered IV in a 7-day rat toxicity study did not show any test article-related changes. The no-observed-adverse-effect level in rats was ≥ 333 µg/kg/day which provides a margin 1000-fold over an anticipated maximum clinical dose of 0.333 µg/kg. Additionally, the MK-6240 formulation was not hemolytic in human or Wistar rat blood. [18F]MK-6240 activity was widely distributed to the brain and the rest of the body, with organ absorbed doses largest for the gall bladder (202 µGy/MBq). The average (±SD) effective dose was 29.4 ± 0.6 µSv/MBq, which is in the typical range for F-18 radiolabeled ligands.

CONCLUSIONS:

Microdoses of [18F]MK-6240 are safe for clinical positron emission tomography imaging studies. Single IV administration of 185 MBq (5 mCi) [18F]MK-6240 is anticipated to result in a total human effective dose of 5.4 mSv and thus allows multiple positron emission tomography scans of the same subject per year.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Radiometria / Radioisótopos de Flúor / Emaranhados Neurofibrilares / Imagem Corporal Total / Doença de Alzheimer / Tomografia por Emissão de Pósitrons combinada à Tomografia Computadorizada / Isoquinolinas Tipo de estudo: Evaluation_studies Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Radiometria / Radioisótopos de Flúor / Emaranhados Neurofibrilares / Imagem Corporal Total / Doença de Alzheimer / Tomografia por Emissão de Pósitrons combinada à Tomografia Computadorizada / Isoquinolinas Tipo de estudo: Evaluation_studies Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article