Alex Satz, senior director, DEL strategy and operations, WuXi AppTec Satz talked about WuXi AppTec’s launch of the HitS (Hit Success) business unit, designed to serve client needs in early stage drug discovery. WuXi’s goals are to provide more and higher-quality hit molecules against targets of interest and to help set the stage for follow-up medical-chemistry optimization. The unit works with all protein target classes, including solubilized membrane proteins and challenging protein complexes. A core strength of the HitS business…
Author Archives: BPI Contributor
GPEx Boost: A Novel Approach for High-Expressing CHO Cell-Line Engineering
Gregory Bleck, PhD, global head of R&D, biologics, Catalent Catalent’s GPEx Boost technology, based on the company’s GPEx technology, is used for engineering high-expressing Chinese hamster ovary (CHO) cells for pharmaceutical production. Using replication and retrovector technology, genes are inserted into mammalian cell lines. The process requires neither antibiotic selection nor use of toxic compounds for gene amplification to make genetically stable cell lines, so stability testing can be kept off of the critical path for some programs. To date,…
CRISPR Library Screens for Oncology Target Discovery at WuXi AppTec
Yong Cang, professor of cancer cell biology, Shanghai Tech University (China) and scientific advisor, WuXi AppTec Because cancer is a genetic disease, Cang observed, researchers are trying systematically to identify genes that enable cancerous propagation. That often requires studying how familiar genes are expressed in vitro. But such cellular behavior can change under different experimental conditions: e.g., when cells are cultured in two- or three-dimensional bioreactors and when studies involve therapeutic compounds or T cells. Cang suggested that researchers might be…
Solutions for Rapid Development and Manufacturing Responses to COVID-19 and Other Public Health Threats
Richard W. Welch, PhD, vice president of development services, Emergent BioSolutions Welch focused on elements of pandemic preparedness. Emergent has a history of working with the US government on bioterrorism and biodefense preparedness, with a focus in recent years on developing platform-based responses to emerging disease threats. Emergent is focusing on therapeutics and vaccines to respond to COVID-19. The company’s therapeutic business unit uses the company’s internal hyperimmune process to generate therapeutics from the plasma of recovering donors, leveraging an…
A Holistic and Integrated CMC Development Approach: Committing to Quality, Reliability, and Speed
Jerry Yang, senior vice president and general manager, HJB International Yang introduced his company, HJB, as an integrated contract and development manufacturing organization (CDMO) with business centers in Boston, San Francisco, and Shanghai. The manufacturing site in Hangzhou City is about an hour-long drive from Shanghai City. The company’s mission is to maintain a global quality business standard, developing innovative technology to balance low costs with high quality, and to serve as a flexible, efficient, and reliable partner. Integrated platforms…
New Business and Funding Models to Accelerate Development of Life-Preserving Therapies
Jonathan Freeman, PhD, founder and COO, Anthos Therapeutics, and senior advisor, Blackstone Life Sciences; and Abdelaziz Toumi, PhD, head of Ibex design and development, customer solutions, Lonza Pharma & Biotech Freeman spoke about the history and philosophy of Anthos and its core program, focusing on specific needs of virtual biotechnology companies particularly from an investor standpoint. Anthos was created after the formation of Blackstone Life Sciences, in collaboration with Novartis. Blackstone’s goal is to find innovative financing approaches that enable…
An End-to-End Integrated-Solutions Approach to Commercial Viral Vector Manufacturing
Jeremy Rautenbach, global product manager, Biotech Integrated Solutions, Pall Biotech Rautenbach emphasized the importance of timely decision-making in the context of viral vector manufacturing. He stressed the importance of quantifying requirements for biomanufacturing skills early in a process and showed how platform approaches can accelerate market entry and reduce risks to ensure manufacturing readiness at the point of approval. Key operational decisions can be well-informed, planned for, and executed by the time a drug is intended to be approved. Committing…
Securing Your Manufacturing Capacity During the Pandemic
Richard Lee, head of the drug product business unit, Samsung Biologics Lee spoke about the evolution of drug-product contract manufacturing and how the business has transformed in response to the ongoing coronovirus pandemic. He spoke about how COVID-19 affected life in South Korea described changes his company has made in how it approached sales, technology transfer, and manufacturing operations. As he put it, “Everything has changed.†South Korea was one of the first affected countries from China’s initial outbreak. Its…
Leveraging Infrastructure Investments and Innovation to Accelerate Biologics Development
Paul Jorjorian, vice president/general manager, biologics, Thermo Fisher Scientific Jorjorian began by noting current trends in drug development, including more compounds being held for longer periods of time than in previous years by small and emerging pharmaceutical and biotechnology companies. He sees an increased complexity of molecules being brought to market, including bispecific antibodies and fusion proteins. Growth continues in both the cell and gene therapy segments and in orphan drug markets. From a business-dynamics perspective, such growth can create…
Viral Vector Empty Versus Full and Plasmid Quantitation Analytics for Accelerated Gene Therapy Time to Market
This webcast features: Joe Ferraiolo, Associate Director, Bioanalytics Applications, C Technologies, a Repligen Company Analytical technologies play a crucial role in accelerating gene therapy speed to market. Dilution steps during protein and DNA quantitation measurements represent the single highest source of accuracy and precision errors. The SoloVPE® device provides a dilution-free workflow that saves time, reduces deviations, and facilitates multisite alignment. Multiple case studies from major biopharmaceutical companies describe execution in process development, analytical labs, and directly on good manufacturing…