Catalent will add five additional Phase III through to commercial-scale manufacturing suites to its gene therapy campus in Harmans, Maryland. The US contract development and manufacturing organization (CDMO) cited growing customer pipelines and an increase in demand as the driver for the investment. Randy Hendrickson, VP Commercial Operations, Catalent Cell & Gene Therapy told us: “Upon completion in the first half of 2022, the facility will house multiple cGMP manufacturing suites with pre-seed, bioreactor, and downstream rooms alongside fill/finish, testing,…
Author Archives: Gareth Macdonald
VMIC to help Oxford Biomedica up capacity for AstraZeneca AZD1222 deal
Oxford Biomedica will make extra production suites at its Oxbox facility available to AstraZeneca to service an expanded coronavirus vaccine manufacturing agreement. AstraZeneca originally hired UK-based contract development and manufacturing organization (CDMO) Oxford Biomedica for the commercial production of the vector-based COVID-19 vaccine candidate, AZD1222 in May. Last week, the Anglo-Swedish biopharmaceutical firm paid an additional £15 million ($20 million) upfront to reserve up to three more manufacturing suites for 18 months. The deal can be extended by mutual agreement.…
Catalent cites biologics as growth driver and forecasts COVID gains in 2021
Catalent says investments in biologics – particularly in the cell and gene therapy space – drove Q4 gains and positioned it as the “go to†COVID CDMO. Catalent’s revenue for the three months ending June was $947.6 million, up 31% on the comparable quarter last year. The contract development and manufacturing organization (CDMO) made a number of purchases in the cell and gene therapy space in recent years. In February, it bought Masthercell from Orgenesis and in 2019 it acquired…
Mesoblast talks Ryoncil, COVID-19 and manufacturing capacity
Mesoblast has sufficient capacity to launch Ryoncil for GVHD but will need to scale-up if the cell therapy works against COVID-19. The Australian firm outlined its manufacturing plan for Ryoncil and other candidates last week during its Q4 call. Ryoncil (remestemcel-L) is a candidate cell therapy for children with steroid-refractory acute graft versus host disease (SR-aGVHD). The product recently received the green light from the US Food and Drug Administration’s Oncologic Drugs Advisory Committee (ODAC), which recommended it be approved…
New technologies can solve downstream bottlenecks says expert
Biopharma needs to embrace new downstream processing technologies to overcome its manufacturing issues, according to an expert. Industry is reluctant to adopt new downstream technologies because firms prefers systems with which staff are familiar, said Alois Jungbauer from the Austrian Centre of Industrial Biotechnology at the University of Natural Resources and Life Sciences. He began by asking delegates at the BPI Europe virtual conference in July: “Why is chromatography so popular? “It’s the high selectivity. It’s the high resolution. We…
Automation can help biopharma enjoy the benefits of continuous processing says CPI
Automation can eliminate downstream bottlenecks and help pharma cut costs says the team behind a continuous downstream processing system at the UK Centre for Process Innovation. Manufacturing biopharmaceutical is a complex, time consuming and costly process. Most products are produced in batches – production runs through a series of steps and then ends. Batch production is reliable and able to make consistent product. However, it can be slow and expensive according to Stuart Jamieson, head of research at the CPI,…
Agilent predicts $750 million global oligo market by 2025 and ups capacity
Agilent Technologies has announced plans to more than double nucleic acid-based drug production capacity at its facility in Frederick, Colorado. The research, development and manufacturing company said it will invest $150 million to add 25,000 square feet of capacity. Agilent cited the growing market for “oligos†as the driver for the investment, predicting it will grow in double digits and be worth more than $750 million by 2025. Sam Raha, president of Agilent’s Diagnostics and Genomics Group, said, “Adding this higher-volume…
Galaxy Life Sciences buys plot on Reactory campus for biopharma plant
Biopharma factory developer Galaxy Life Sciences has bought a plot at an emerging biomanufacturing hub in Worcester, Massachusetts. The deal will see Galaxy build a $50 million facility to support research, development and manufacture of biopharmaceuticals or pharmaceuticals according to the Worcester Business Development Corporation, the organization that runs the “Reactory†campus. Galaxy CEO Mike O’Brien told us “We are talking to several tenants already and expect to have a commitment from at least one in the next month or…
Ligand strikes $516m deal to buy Pfenex for expression tech
Ligand Pharmaceutical will buy Pfenex to add the latter’s protein expression technology to its core drug discovery and formulation business. The deal – worth $516 million – is expected to complete before the end of the year. Ligand cited Pfenex’s expression technology as a major motivation for the deal, pointing out it is out-licensed for numerous commercial and development-stage programs. CEO John Higgins likened the deal to Ligand’s acquisition of the technology Captisol – gained when the firm bought Cydex…
The CHO must go on? Bioinformatics and gene editing reshaping cell line dev
Computational analysis and gene editing will yield CHO cells able to make protein drugs, faster and more cheaply says expert. The ability to turn cells into protein production “factories†is the foundation of modern biopharma according to Bjørn Voldborg, director of CHO cell line development at the Technical University of Denmark. “If you want to engineer a factory [cell line] you need to understand what machines you have in the factory. It’s the genome sequences of the CHO cells –…