Formulation Considerations for Autologous T Cell Drug Products

Genetically modified autologous T cells have become an established immunotherapy in the fight against cancer. The manufacture of chimeric antigen receptor (CAR) and αβ-T cell receptor (TCR) transduced T cells poses unique challenges, including the formulation, cryopreservation and fill–finish steps,...

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Main Authors: Christopher F. van der Walle, Sonya Godbert, Gabriele Saito, Zein Azhari
Format: Article
Language:English
Published: MDPI AG 2021-08-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/13/8/1317
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spelling doaj-7e281b717721464ab41da4ccbe7537432021-08-26T14:13:27ZengMDPI AGPharmaceutics1999-49232021-08-01131317131710.3390/pharmaceutics13081317Formulation Considerations for Autologous T Cell Drug ProductsChristopher F. van der Walle0Sonya Godbert1Gabriele Saito2Zein Azhari3GSK R&D, Gunnels Wood, Stevenage, Herts SG1 2NY, UKGSK R&D, Gunnels Wood, Stevenage, Herts SG1 2NY, UKGSK R&D, Gunnels Wood, Stevenage, Herts SG1 2NY, UKGSK R&D, Gunnels Wood, Stevenage, Herts SG1 2NY, UKGenetically modified autologous T cells have become an established immunotherapy in the fight against cancer. The manufacture of chimeric antigen receptor (CAR) and αβ-T cell receptor (TCR) transduced T cells poses unique challenges, including the formulation, cryopreservation and fill–finish steps, which are the focus of this review. With an increasing number of marketing approvals for CAR-T cell therapies, comparison of their formulation design and presentation for administration can be made. These differences will be discussed alongside the emergence of automated formulation and fill-finish processes, the formulation design space, Monte Carlo simulation applied to risk analysis, primary container selection, freezing profiles and thaw and the use of dimethyl sulfoxide and alternative solvents/excipients as cryopreservation agents. The review will conclude with a discussion of the pharmaceutical solutions required to meet the simplification of manufacture and flexibility in dosage form for clinical treatment.https://www.mdpi.com/1999-4923/13/8/1317closed processfill–finishdesign spaceprimary containercryopreservationfreeze–thaw
collection DOAJ
language English
format Article
sources DOAJ
author Christopher F. van der Walle
Sonya Godbert
Gabriele Saito
Zein Azhari
spellingShingle Christopher F. van der Walle
Sonya Godbert
Gabriele Saito
Zein Azhari
Formulation Considerations for Autologous T Cell Drug Products
Pharmaceutics
closed process
fill–finish
design space
primary container
cryopreservation
freeze–thaw
author_facet Christopher F. van der Walle
Sonya Godbert
Gabriele Saito
Zein Azhari
author_sort Christopher F. van der Walle
title Formulation Considerations for Autologous T Cell Drug Products
title_short Formulation Considerations for Autologous T Cell Drug Products
title_full Formulation Considerations for Autologous T Cell Drug Products
title_fullStr Formulation Considerations for Autologous T Cell Drug Products
title_full_unstemmed Formulation Considerations for Autologous T Cell Drug Products
title_sort formulation considerations for autologous t cell drug products
publisher MDPI AG
series Pharmaceutics
issn 1999-4923
publishDate 2021-08-01
description Genetically modified autologous T cells have become an established immunotherapy in the fight against cancer. The manufacture of chimeric antigen receptor (CAR) and αβ-T cell receptor (TCR) transduced T cells poses unique challenges, including the formulation, cryopreservation and fill–finish steps, which are the focus of this review. With an increasing number of marketing approvals for CAR-T cell therapies, comparison of their formulation design and presentation for administration can be made. These differences will be discussed alongside the emergence of automated formulation and fill-finish processes, the formulation design space, Monte Carlo simulation applied to risk analysis, primary container selection, freezing profiles and thaw and the use of dimethyl sulfoxide and alternative solvents/excipients as cryopreservation agents. The review will conclude with a discussion of the pharmaceutical solutions required to meet the simplification of manufacture and flexibility in dosage form for clinical treatment.
topic closed process
fill–finish
design space
primary container
cryopreservation
freeze–thaw
url https://www.mdpi.com/1999-4923/13/8/1317
work_keys_str_mv AT christopherfvanderwalle formulationconsiderationsforautologoustcelldrugproducts
AT sonyagodbert formulationconsiderationsforautologoustcelldrugproducts
AT gabrielesaito formulationconsiderationsforautologoustcelldrugproducts
AT zeinazhari formulationconsiderationsforautologoustcelldrugproducts
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