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analyse marché; Market analysis, pipeline, market overview

Cell and gene therapies

Every month, MabDesign’s market analyses provide you with an overview of market dynamics and projects in development for a specific indication or technology, to help you better understand the constantly evolving market for biomedicines and biomanufacturing.

The first edition of our Innovations for Cell and Gene Therapies (ICGT) congress, organized in collaboration with the French Society of Cell and Gene Therapy (SFTCG) will take place on May 22, 2024, in Paris. In the meantime, this month we share an overview of the cell and gene therapy market.

Advanced therapy medicinal products (ATMPs) explore new therapeutic approaches based on genome modification or the manipulation of patient or healthy donor cells. They represent a major transition from traditional medicine to a more personalized, targeted approach. These innovative products are accelerating the development of biotherapies, and currently account for around a third of all biopharmaceuticals under development .

The market for in vivo gene therapy

In vivo gene therapy products (excluding genetically modified cell therapies such as CAR-T) are few on the market, with just 12 products currently available. On the other hand, the pipeline is quite extensive, with 2107 gene therapies in development. The vast majority of projects are in the early stages of development, with only 15% in clinical phases. In terms of vectors used, viral vectors, and in particular AAVs(adeno-associated viruses), are the technology most frequently chosen for projects in the pipeline.

in vivo gene therapies on the market*.
0
products under development*
0

*excluding genetically modified cell therapies

In vivo gene therapies in development, by phase

Vector types (pipeline)

vecteurs viraux, vecteurs non viraux, AAVs, thérapie génique, lentivirus, LNP, nanoparticules, plasmide

AV: adenovirus; AAV: adeno-associated virus; LNP: lipid nanoparticles

The market for gene-modified cell therapies

Gene-modified cell therapies (or ex-vivo gene therapies), such as CAR-T cells, are still few on the market: there are currently 17 products available. By contrast, the pipeline is very rich, with over 3,000 genetically modified cell therapies in development. Projects are in relatively advanced stages of development, with 36% in clinical phases. In terms of targeted indications, the first three are blood cancers : diffuse large B-cell lymphoma, acute B-cell lymphocytic leukemia, and relapsed/refractory multiple myeloma.

gene-modified cell therapies on the market
0
products in development
0

Gene-modified cell therapies in development, by phase

Top 3 indications (pipeline)

gene-modified cell therapy, CAR-T, thérapie cellulaire génétiquement modifiées, thérapie génique ex-vivo

The Cell Therapy Market

More cell therapy drugs are on the market: there are currently 41 marketed products and 1,894 cell therapies in development. Compared with gene therapies, 46.1% of cell therapies in development are in clinical phases. The most targeted therapeutic areas are oncology, the central nervous system and infectious diseases.

cell therapies on the market
0
products in development
0

Cell therapies in development, by phase

Top 3 therapeutic areas (pipeline)

aires thérapeutiques, thérapies cellulaires, pipeline, indications

Download our infographic

Cell and gene therapy market

thérapie cellulaire, thérapie génique, marché, pipeline, ICGT

Want to find out more?

ICGT, Cell & Gene therapy congress, MabDesign

In 2024, in collaboration with the SFTCG, MabDesign is launching the first edition of the Innovations for Cell and Gene Therapies (ICGT) congress! You canregisternow, or contact us for more information.

MabDesign has acquired and cultivates its expertise in all market segments associated with biopharmaceuticals and biomanufacturing. Our team of consultants is at your disposal to support you in all your biotherapy-related projects. Feel free to explore our range of services, including our marketing and strategic analyses, if you’d like to find out more!

Sources: MabDesign, GlobalData

Date – March 2024

Jean-Roch Fabreguettes

MEARY

Directeur Médical et Personne Responsable du Centre MEARY de thérapie cellulaire et génique au sein de l’hôpital Saint-Louis à Paris

Jean-Roch Fabreguettes est un spécialiste de la recherche translationnelle et des phases précoces de développement clinique des médicaments de thérapie innovantes (MTI). Pharmacien, titulaire d’un doctorat de l’Université de Montpellier 1, il a travaillé plus de 25 ans dans le domaine et a contribué, pour des équipes académiques comme pour des start-ups, à la réalisation de plus de 30 programmes de recherche sur différents types de MTI : thérapie génique in vivo ou ex vivo, thérapie cellulaire, ingénierie tissulaire… Il est actuellement Directeur Médical et Personne Responsable du Centre MEARY de thérapie cellulaire et génique au sein de l’hôpital Saint-Louis à Paris. Le centre MEARY est une plateforme de l’Assistance Publique – Hôpitaux de Paris (AP-HP), dédiée à la fabrication de médicament de thérapie innovante expérimentaux. Laboratoire membre de l’ISCT, il est autorisé par l’ANSM et dispose d’un certificat GMP. A ce titre Jean-Roch Fabreguettes est impliqué dans le développement clinique et la fabrication de nombreux MTI : CAR-T cells, lymphocytes T régulateurs, cellules stromales mésenchymateuses…

Précédemment, Jean-Roch Fabreguettes a été expert Qualité (CMC) auprès de l’ANSM durant 9 ans et a conseillé différentes sociétés de biotechnologies. Il est un intervenant régulier pour l’Université Paris Cité et un membre actif de l’ISCT et de réseaux nationaux et internationaux sur les MTI (UNI-TC, Join4ATMP).