Industry Perspective on the Pharmacokinetic and Absorption, Distribution, Metabolism, and Excretion Characterization of Heterobifunctional Protein Degraders.


Journal

Drug metabolism and disposition: the biological fate of chemicals
ISSN: 1521-009X
Titre abrégé: Drug Metab Dispos
Pays: United States
ID NLM: 9421550

Informations de publication

Date de publication:
Jul 2023
Historique:
received: 24 02 2023
accepted: 05 04 2023
medline: 19 6 2023
pubmed: 12 4 2023
entrez: 11 4 2023
Statut: ppublish

Résumé

Targeted protein degraders (TPDs), specifically the bifunctional protein degraders discussed in this manuscript, consist of two linked ligands for a protein of interest and an E3 ligase, resulting in molecules that largely violate accepted physicochemical limits (e.g., Lipinski's Rule of Five) for oral bioavailability. In 2021, the IQ Consortium Degrader DMPK/ADME Working Group undertook a survey of 18 IQ member and nonmember companies working on degraders to understand whether the characterization and optimization of these molecules were different from any other beyond the Rule of Five (bRo5) compounds. Additionally, the working group sought to identify pharmacokinetic (PK)/absorption, distribution, metabolism, and excretion (ADME) areas in need of further evaluation and where additional tools could aid in more rapid advancement of TPDs to patients. The survey revealed that although TPDs reside in a challenging bRo5 physicochemical space, most respondents focus their efforts on oral delivery. Physicochemical properties required for oral bioavailability were generally consistent across the companies surveyed. Many of the member companies used modified assays to address challenging degrader properties (e.g., solubility, nonspecific binding), but only half indicated that they modified their drug discovery workflows. The survey also suggested the need for further scientific investigation in the areas of central nervous system penetration, active transport, renal elimination, lymphatic absorption, in silico/machine learning, and human pharmacokinetic prediction. Based on the survey results, the Degrader DMPK/ADME Working Group concluded that TPD evaluation does not fundamentally differ from other bRo5 compounds but requires some modification compared with traditional small molecules and proposes a generic workflow for PK/ADME evaluation of bifunctional TPDs. SIGNIFICANCE STATEMENT: Based on an industry survey, this article provides an understanding of the current state of absorption, distribution, metabolism, and excretion science pertaining to characterizing and optimizing targeted protein degraders, specifically bifunctional protein degraders, based upon responses by 18 IQ consortium members and non-members developing targeted protein degraders. Additionally, this article puts into context the differences / similarities in methods and strategies utilized for heterobifunctional protein degraders compared to other beyond Rule of Five molecules and conventional small molecule drugs.

Identifiants

pubmed: 37041086
pii: dmd.122.001154
doi: 10.1124/dmd.122.001154
doi:

Substances chimiques

Ubiquitin-Protein Ligases EC 2.3.2.27

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

792-803

Informations de copyright

Copyright © 2023 by The American Society for Pharmacology and Experimental Therapeutics.

Auteurs

Laurie P Volak (LP)

Janssen Research & Development, LLC, San Diego, California (L.P.V.); The Healthcare Business of Merck KGaA, Darmstadt, Germany (H.M.D.); Amgen Inc, San Francisco, California (S.H.); Novartis Institutes for Biomedical Research, Cambridge, Massachusetts (D.N.); AbbVie Inc, North Chicago, Illinois (C.P.); AstraZeneca, Cambridge, United Kingdom (A.P.); Roche pRED, Basel, Switzerland (C.R.); GlaxoSmithKline, Stevenage, United Kingdom (P.S.-S.); Genentech, San Francisco, California (D.Z.); and Takeda Development Center Americas, San Diego, California (M.Z.) lvolak@rapportrx.com.

Heide Marika Duevel (HM)

Janssen Research & Development, LLC, San Diego, California (L.P.V.); The Healthcare Business of Merck KGaA, Darmstadt, Germany (H.M.D.); Amgen Inc, San Francisco, California (S.H.); Novartis Institutes for Biomedical Research, Cambridge, Massachusetts (D.N.); AbbVie Inc, North Chicago, Illinois (C.P.); AstraZeneca, Cambridge, United Kingdom (A.P.); Roche pRED, Basel, Switzerland (C.R.); GlaxoSmithKline, Stevenage, United Kingdom (P.S.-S.); Genentech, San Francisco, California (D.Z.); and Takeda Development Center Americas, San Diego, California (M.Z.).

Sara Humphreys (S)

Janssen Research & Development, LLC, San Diego, California (L.P.V.); The Healthcare Business of Merck KGaA, Darmstadt, Germany (H.M.D.); Amgen Inc, San Francisco, California (S.H.); Novartis Institutes for Biomedical Research, Cambridge, Massachusetts (D.N.); AbbVie Inc, North Chicago, Illinois (C.P.); AstraZeneca, Cambridge, United Kingdom (A.P.); Roche pRED, Basel, Switzerland (C.R.); GlaxoSmithKline, Stevenage, United Kingdom (P.S.-S.); Genentech, San Francisco, California (D.Z.); and Takeda Development Center Americas, San Diego, California (M.Z.).

David Nettleton (D)

Janssen Research & Development, LLC, San Diego, California (L.P.V.); The Healthcare Business of Merck KGaA, Darmstadt, Germany (H.M.D.); Amgen Inc, San Francisco, California (S.H.); Novartis Institutes for Biomedical Research, Cambridge, Massachusetts (D.N.); AbbVie Inc, North Chicago, Illinois (C.P.); AstraZeneca, Cambridge, United Kingdom (A.P.); Roche pRED, Basel, Switzerland (C.R.); GlaxoSmithKline, Stevenage, United Kingdom (P.S.-S.); Genentech, San Francisco, California (D.Z.); and Takeda Development Center Americas, San Diego, California (M.Z.).

Colin Phipps (C)

Janssen Research & Development, LLC, San Diego, California (L.P.V.); The Healthcare Business of Merck KGaA, Darmstadt, Germany (H.M.D.); Amgen Inc, San Francisco, California (S.H.); Novartis Institutes for Biomedical Research, Cambridge, Massachusetts (D.N.); AbbVie Inc, North Chicago, Illinois (C.P.); AstraZeneca, Cambridge, United Kingdom (A.P.); Roche pRED, Basel, Switzerland (C.R.); GlaxoSmithKline, Stevenage, United Kingdom (P.S.-S.); Genentech, San Francisco, California (D.Z.); and Takeda Development Center Americas, San Diego, California (M.Z.).

Andy Pike (A)

Janssen Research & Development, LLC, San Diego, California (L.P.V.); The Healthcare Business of Merck KGaA, Darmstadt, Germany (H.M.D.); Amgen Inc, San Francisco, California (S.H.); Novartis Institutes for Biomedical Research, Cambridge, Massachusetts (D.N.); AbbVie Inc, North Chicago, Illinois (C.P.); AstraZeneca, Cambridge, United Kingdom (A.P.); Roche pRED, Basel, Switzerland (C.R.); GlaxoSmithKline, Stevenage, United Kingdom (P.S.-S.); Genentech, San Francisco, California (D.Z.); and Takeda Development Center Americas, San Diego, California (M.Z.).

Caroline Rynn (C)

Janssen Research & Development, LLC, San Diego, California (L.P.V.); The Healthcare Business of Merck KGaA, Darmstadt, Germany (H.M.D.); Amgen Inc, San Francisco, California (S.H.); Novartis Institutes for Biomedical Research, Cambridge, Massachusetts (D.N.); AbbVie Inc, North Chicago, Illinois (C.P.); AstraZeneca, Cambridge, United Kingdom (A.P.); Roche pRED, Basel, Switzerland (C.R.); GlaxoSmithKline, Stevenage, United Kingdom (P.S.-S.); Genentech, San Francisco, California (D.Z.); and Takeda Development Center Americas, San Diego, California (M.Z.).

Paul Scott-Stevens (P)

Janssen Research & Development, LLC, San Diego, California (L.P.V.); The Healthcare Business of Merck KGaA, Darmstadt, Germany (H.M.D.); Amgen Inc, San Francisco, California (S.H.); Novartis Institutes for Biomedical Research, Cambridge, Massachusetts (D.N.); AbbVie Inc, North Chicago, Illinois (C.P.); AstraZeneca, Cambridge, United Kingdom (A.P.); Roche pRED, Basel, Switzerland (C.R.); GlaxoSmithKline, Stevenage, United Kingdom (P.S.-S.); Genentech, San Francisco, California (D.Z.); and Takeda Development Center Americas, San Diego, California (M.Z.).

Donglu Zhang (D)

Janssen Research & Development, LLC, San Diego, California (L.P.V.); The Healthcare Business of Merck KGaA, Darmstadt, Germany (H.M.D.); Amgen Inc, San Francisco, California (S.H.); Novartis Institutes for Biomedical Research, Cambridge, Massachusetts (D.N.); AbbVie Inc, North Chicago, Illinois (C.P.); AstraZeneca, Cambridge, United Kingdom (A.P.); Roche pRED, Basel, Switzerland (C.R.); GlaxoSmithKline, Stevenage, United Kingdom (P.S.-S.); Genentech, San Francisco, California (D.Z.); and Takeda Development Center Americas, San Diego, California (M.Z.).

Michael Zientek (M)

Janssen Research & Development, LLC, San Diego, California (L.P.V.); The Healthcare Business of Merck KGaA, Darmstadt, Germany (H.M.D.); Amgen Inc, San Francisco, California (S.H.); Novartis Institutes for Biomedical Research, Cambridge, Massachusetts (D.N.); AbbVie Inc, North Chicago, Illinois (C.P.); AstraZeneca, Cambridge, United Kingdom (A.P.); Roche pRED, Basel, Switzerland (C.R.); GlaxoSmithKline, Stevenage, United Kingdom (P.S.-S.); Genentech, San Francisco, California (D.Z.); and Takeda Development Center Americas, San Diego, California (M.Z.).

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