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Development of extracellular vesicle-based medicinal products: A position paper of the group "Extracellular Vesicle translatiOn to clinicaL perspectiVEs - EVOLVE France".

Authors :
Silva AKA
Morille M
Piffoux M
Arumugam S
Mauduit P
Larghero J
Bianchi A
Aubertin K
Blanc-Brude O
Noël D
Velot E
Ravel C
Elie-Caille C
Sebbagh A
Boulanger C
Wilhelm C
Rahmi G
Raymond-Letron I
Cherukula K
Montier T
Martinaud C
Bach JM
Favre-Bulle O
Spadavecchia J
Jorgensen C
Menasché P
Aussel C
Chopineau J
Mosser M
Ullah M
Sailliet N
Luciani N
Mathieu N
Rautou PE
Brouard S
Boireau W
Jauliac S
Dedier M
Trouvin JH
Gazeau F
Trouillas M
Peltzer J
Monsel A
Banzet S
Source :
Advanced drug delivery reviews [Adv Drug Deliv Rev] 2021 Dec; Vol. 179, pp. 114001. Date of Electronic Publication: 2021 Oct 19.
Publication Year :
2021

Abstract

Extracellular vesicles (EV) are emergent therapeutic effectors that have reached clinical trial investigation. To translate EV-based therapeutic to clinic, the challenge is to demonstrate quality, safety, and efficacy, as required for any medicinal product. EV research translation into medicinal products is an exciting and challenging perspective. Recent papers, provide important guidance on regulatory aspects of pharmaceutical development, defining EVs for therapeutic applications and critical considerations for the development of potency tests. In addition, the ISEV Task Force on Regulatory Affairs and Clinical Use of EV-based Therapeutics as well as the Exosomes Committee from the ISCT are expected to contribute in an active way to the development of EV-based medicinal products by providing update on the scientific progress in EVs field, information to patients and expert resource network for regulatory bodies. The contribution of our work group "Extracellular Vesicle translatiOn to clinicaL perspectiVEs - EVOLVE France", created in 2020, can be positioned in complement to all these important initiatives. Based on complementary scientific, technical, and medical expertise, we provide EV-specific recommendations for manufacturing, quality control, analytics, non-clinical development, and clinical trials, according to current European legislation. We especially focus on early phase clinical trials concerning immediate needs in the field. The main contents of the investigational medicinal product dossier, marketing authorization applications, and critical guideline information are outlined for the transition from research to clinical development and ultimate market authorization.<br />Competing Interests: Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Florence Gazeau, Amanda Karine Andriola Silva, Claire Wilhelm and Gabriel Rahmi are co-founders of the spin-off Evora Biosciences. Amanda Karine Andriola Silva and Claire Wilhelm are co-founders of the spin-off EverZom. Max Piffoux is consultant and owns stocks in the spin-off Evora Biosciences and in the spin-off EverZom.<br /> (Copyright © 2021 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1872-8294
Volume :
179
Database :
MEDLINE
Journal :
Advanced drug delivery reviews
Publication Type :
Academic Journal
Accession number :
34673131
Full Text :
https://doi.org/10.1016/j.addr.2021.114001