|Webcasts|April 10, 2023

A customized approach to mRNA manufacturing

Author(s)Curia

Webinar Date/Time: Wed, May 10, 2023 11:00 AM EDT

Participate in this webinar to gain insights into methods for furthering mRNA production programs and learn how to identify areas for development and streamline processes.

Register Free: https://www.biopharminternational.com/bp_w/customized-approach

Event Overview:

Diversity in mRNA therapies has mitigated advancements in the processes for manufacturing. IVT and capping reactions are not universal and must be finely tuned to each molecule based on composition, structure, and size. Using literature and experimental design, adapting each method to fit the molecule is necessary for hastening the optimization of mRNA development. In this webinar, you will gain insights into:

  • Subject examination
  • Identifying vital methodologies
  • Refining and focusing target components
  • Proper in-process analytics

Key Learning Objectives

  • Identifying the variable/critical components involved in the mRNA production process
  • Understanding the reasoning behind revisiting procedures
  • Learning what metrics to use to navigate the mRNA process development

Who Should Attend

  • Students/Researchers interested in developing better methods of in vitro transcribed RNA manufacturing


Speaker


Scott Alderucci
Director of mRNA Process Development & GMP operations
Curia Global, Inc.

Scott Alderucci is the director of process development overseeing the Process Development and GMP divisions of mRNA at Curia. He holds a scientific master’s degree and has 25 years of experience working in the field of biologics focused on DNA, mRNA and antibody platforms. He has worked within such institutions as Millennium Pharmaceuticals, Cellular Genomics, the State of Massachusetts, and Shire Pharmaceuticals prior to joining Curia. His current role is focused on providing research and development through GMP level production of a wide range of mRNA products to meet various program goals.

Register Free: https://www.biopharminternational.com/bp_w/customized-approach


Related to this article

The BioPharm Brief: A Bispecific Approval in Head and Neck Cancer, TCR Bispecifics Head to the Clinic, and a New Antibody Target in Essential Thrombocythemia
FDA grants accelerated approval to Johnson & Johnson’s subcutaneous EGFR/MET bispecific Rybrevant Faspro for previously treated head and neck squamous cell carcinoma, T-Therapeutics raises a $133 million Series B to take TCR-CD3 bispecifics into clinical trials, and Alethio Therapeutics raises a $90 million Series A to advance its first-in-class G6B antibody for essential thrombocythemia.
The BioPharm Brief: Ivonescimab Priority Review in China, Stargardt Gene Therapy Moves Toward Phase 3, and Longer Dosing Intervals for an IBD Bispecific
China’s NMPA grants priority review to Akeso’s PD-1/VEGF bispecific ivonescimab with chemotherapy for first-line biliary tract cancer, VeonGen Therapeutics aligns with FDA on a phase 3 design for its dual-AAV Stargardt gene therapy VG801, and Caldera Therapeutics’ IL-23p19×TL1A bispecific CLD-423 shows a half-life of more than 40 days in a phase 1a trial.