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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Online Access: | https://www.mdpi.com/1999-4923/13/8/1317 |
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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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1721190687086477312 |