Assessing the risk of a clinically significant infection from a Microneedle Array Patch (MAP) product.


Journal

Journal of controlled release : official journal of the Controlled Release Society
ISSN: 1873-4995
Titre abrégé: J Control Release
Pays: Netherlands
ID NLM: 8607908

Informations de publication

Date de publication:
09 2023
Historique:
received: 17 03 2023
revised: 28 06 2023
accepted: 01 07 2023
medline: 11 9 2023
pubmed: 13 7 2023
entrez: 12 7 2023
Statut: ppublish

Résumé

Microneedle Array Patches (MAPs) are an emerging dosage form that creates transient micron-sized disruptions in the outermost physical skin barrier, the stratum corneum, to facilitate delivery of active pharmaceutical ingredients to the underlying tissue. Numerous MAP products are proposed and there is significant clinical potential in priority areas such as vaccination. However, since their inception scientists have hypothesized about the risk of a clinically significant MAP-induced infection. Safety data from two major Phase 3 clinical trials involving hundreds of participants, who in total received tens of thousands of MAP applications, does not identify any clinically significant infections. However, the incumbent data set is not extensive enough to make definitive generalizable conclusions. A comprehensive assessment of the infection risk is therefore advised for MAP products, and this should be informed by clinical and pre-clinical data, theoretical analysis and informed opinions. In this article, a group of key stakeholders identify some of the key product- and patient-specific factors that may contribute to the risk of infection from a MAP product and provide expert opinions in the context of guidance from regulatory authorities. Considerations that are particularly pertinent to the MAP dosage form include the specifications of the finished product (e.g. microbial specification), it's design features, the setting for administration, the skill of the administrator, the anatomical application site, the target population and the clinical context. These factors, and others discussed in this article, provide a platform for the development of MAP risk assessments and a stimulus for early and open dialogue between developers, regulatory authorities and other key stakeholders, to expedite and promote development of safe and effective MAP products.

Identifiants

pubmed: 37437849
pii: S0168-3659(23)00425-X
doi: 10.1016/j.jconrel.2023.07.001
pii:
doi:

Substances chimiques

Pharmaceutical Preparations 0

Types de publication

Letter Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

236-245

Subventions

Organisme : World Health Organization
ID : 001
Pays : International

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest Prausnitz is an inventor of patents, founder/shareholder of companies, and consultant to companies developing MAP technologies. This conflict of interest is managed by the Georgia Institute of Technology. Coulman and Birchall are inventors of patents. This conflict of interest is managed by Cardiff University.

Auteurs

Maria Dul (M)

Cardiff School of Pharmacy and Pharmaceutical Sciences, Cardiff University, Cardiff, UK.

Mohammed Alali (M)

World Health Organization, Geneva, Switzerland.

Mahmoud Ameri (M)

Americeutics Consulting, USA.

Matthew Douglas Burke (MD)

Stemline Therapeutics Inc, A Menarini Group Company, USA.

Christine M Craig (CM)

ValSource, Inc., USA.

Benjamin Paul Creelman (BP)

PATH, Seattle, USA.

Lisa Dick (L)

Kindeva Drug Delivery, USA.

Ryan F Donnelly (RF)

School of Pharmacy, Queen's University Belfast, Belfast, UK.

Michael N Eakins (MN)

Eakins & Associates, USA.

Collrane Frivold (C)

PATH, Seattle, USA.

Angus Harry Forster (AH)

Vaxxas Pty Ltd., Australia.

Philippe-Alexandre Gilbert (PA)

Bill and Melinda Gates Foundation, Seattle, USA.

Stefan Henke (S)

Dr. Stefan Henke Pharma Consulting, Germany.

Sebastien Henry (S)

Micron Biomedical, Inc., USA.

Desmond Hunt (D)

United States Pharmacopeia, USA.

Hayley Lewis (H)

Zosano Pharma, USA.

Howard I Maibach (HI)

Department of Dermatology, University of California San Francisco, San Francisco, CA, USA.

Jessica Joyce Mistilis (JJ)

PATH, Seattle, USA.

Jung-Hwan Park (JH)

Department of Bionano Technology, Gachon University, Seongnam, Republic of Korea.

Mark R Prausnitz (MR)

School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta, GA, USA.

David Kenneth Robinson (DK)

Bill and Melinda Gates Foundation, Seattle, USA.

Carmen Amelia Rodriguez Hernandez (CAR)

World Health Organization, Geneva, Switzerland.

Charles Ross (C)

Vaxxas Pty Ltd., Australia.

Juyeop Shin (J)

Raphas Co. Ltd, Republic of Korea.

Tycho Joseph Speaker (TJ)

AbbVie, Inc., USA.

Kevin Michael Taylor (KM)

University College London School of Pharmacy, British Pharmacopoeia Commission, UK.

Darin Zehrung (D)

PharmaJet, Inc., USA.

James C Birchall (JC)

Cardiff School of Pharmacy and Pharmaceutical Sciences, Cardiff University, Cardiff, UK.

Courtney Jarrahian (C)

PATH, Seattle, USA.

Sion A Coulman (SA)

Cardiff School of Pharmacy and Pharmaceutical Sciences, Cardiff University, Cardiff, UK. Electronic address: coulmansa@cardiff.ac.uk.

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