Strategies for Identity Testing of Therapeutic Oligonucleotide Drug Substances and Drug Products.

GMP controls identification intact mass measurement oligonucleotides risk assessment sequence confirmation

Journal

Nucleic acid therapeutics
ISSN: 2159-3345
Titre abrégé: Nucleic Acid Ther
Pays: United States
ID NLM: 101562758

Informations de publication

Date de publication:
10 2020
Historique:
pubmed: 29 8 2020
medline: 21 10 2021
entrez: 29 8 2020
Statut: ppublish

Résumé

A risk-based approach for routine identity testing of therapeutic oligonucleotide drug substances and drug products is described. Risk analysis of solid-phase oligonucleotide synthesis indicates that intact mass measurement is a powerful technique for confirming synthesis of the intended oligonucleotide. Further risk assessment suggests that the addition of a second, sequence-sensitive identity test, which relies on a comparison of some property of the sample to a reference standard of proven identity, results in a sufficient test of identity for most oligonucleotide drug substances and products. Alternative strategies for drug product identity testing are presented. The analysis creates a common way to communicate risk and should result in a harmonized approach to identity testing that avoids the unnecessary analytical burden associated with routine

Identifiants

pubmed: 32857010
doi: 10.1089/nat.2020.0878
doi:

Substances chimiques

Oligonucleotides 0
Pharmaceutical Preparations 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

249-264

Auteurs

Daniel Capaldi (D)

Development Chemistry, Ionis Pharmaceuticals Inc., Carlsbad, California, USA.

Nadim Akhtar (N)

New Modalities and Parenteral Development and Pharmaceutical Technology & Development, Operations, AstraZeneca, Macclesfield, United Kingdom.

Tom Atherton (T)

Structure and Function Characterization, CMC Analytical, GlaxoSmithKline, Stevenage, United Kingdom.

David Benstead (D)

Chemical Development, Pharmaceutical Technology & Development, Operations, AstraZeneca, Macclesfield, United Kingdom.

Ayman Charaf (A)

Research and Development Tides, Pharmaceutical Development Platform, Sanofi-Aventis GmbH, Frankfurt am Main, Germany.

Thomas De Vijlder (T)

Analytical Development, Small Molecule Development, Janssen Pharmaceutical Companies of Johnson and Johnson, Beerse, Belgium.

Carl Heatherington (C)

Drug Substance and Product Analysis UK, CMC Analytical, GlaxoSmithKline, Stevenage, United Kingdom.

Joerg Hoernschemeyer (J)

F. Hoffmann-La Roche, Global Supplier Quality, Basel, Switzerland.

Hong Jiang (H)

Analytical Development, Biogen, Cambridge, Massachusetts, USA.

Ulrike Rieder (U)

Technical Research and Development, Global Drug Development, Novartis Pharma, Basel, Switzerland.

Francis Ring (F)

Development Chemistry, Ionis Pharmaceuticals Inc., Carlsbad, California, USA.

Robert Peter (R)

Analytical Research and Development, Synthetic Molecules Technical Development, F. Hoffmann-La Roche, Basel, Switzerland.

Jessica A Stolee (JA)

Analytical Development, Biogen, Cambridge, Massachusetts, USA.

Rainer Wechselberger (R)

Analytical Development, Small Molecule Development, Janssen Pharmaceutical Companies of Johnson and Johnson, Beerse, Belgium.

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Classifications MeSH