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Moving to CoPACaPAnA: Implementation of a continuous protein A capture process for antibody applications within an end-to-end single-use GMP manufacturing downstream process

机译:移动到Copacapana:在端到端单一使用GMP制造下游工艺中实现连续蛋白的抗体应用捕获方法

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For the first time to our knowledge the implementation of a continuous protein A capture process for antibody applications (CoPACaPAnA) embedded in an end-to-end single-use 500 L GMP manufacturing downstream process of a multispecific monoclonal antibody (mAb) using a single-use SMB system was conducted. Throughout the last years, a change concerning the pipelines in pharmaceutical industry could be observed, moving to a more heterogeneous portfolio of antibodies, fusion proteins and nanobodies. Trying to adjust purification processes to these new modalities, a higher degree of flexibility and lower operational and capital expenditure is desired. The implementation of single-use equipment is a favored solution for increasing manufacturing agility and it has been demonstrated that continuous processing can be beneficial concerning processing cost and time. Reducing protein A resin resulted in 59% cost reduction for the protein A step, with additional cost reduction also for the intermediate and polishing step due to usage of disposable technology. The downstream process applied here consisted of three chromatography steps that were all conducted on a single-use SMB system, with the capture step being run in continuous mode while intermediate and polishing was conducted in batch mode. Further, two steps dedicated to virus inactivation/ removal and three filtration steps were performed, yielding around 100 g of drug substance going into clinical phase I testing. Therefore, in this study it has been demonstrated that employing a continuous capture within a GMP single-use downstream processing chain is feasible and worthy of consideration among the biotech industry for future application to modality-diverse pipelines.
机译:首次了解我们使用单一的抗体应用(Copacapana)的连续蛋白的实现捕获方法(Copacapana),使用单一的多特异性单克隆抗体(mAb)的下端使用500μlMMP制造下游过程。 - 使用SMB系统。在过去几年中,可以观察到制药行业管道的变化,移动到更加异质的抗体组合,融合蛋白和纳米型。试图将净化过程调整为这些新的方式,需要更高程度的灵活性和更低的运营和资本支出。单用设备的实施是一种有利于增加制造灵活性的解决方案,并且已经证明了连续处理可以有利于加工成本和时间。减少蛋白质的树脂导致蛋白质的成本降低59%,对于使用一次性技术的使用,额外的成本降低了中间和抛光步骤。这里应用的下游过程包括在一次使用SMB系统上进行的三个色谱步骤,其中捕获步骤以连续模式运行,同时以批速模式进行中间和抛光。此外,进行了两种专用于病毒失活/去除和三个过滤步骤的步骤,得到约100g的药物,进入临床期I测试。因此,在本研究中,已经证明,在GMP单用下游加工链中使用连续捕获是可行的,并且值得在生物技术行业中考虑,以便将来应用于模态多样化的管道。

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