Advancing Cell & Gene Therapies: Overcoming Challenges, Embracing Innovation & Shaping 2025

Advancing Cell & Gene Therapies: Overcoming Challenges, Embracing Innovation & Shaping 2025


TRENDING CONTENT - Catch Up

#1. A Phase-Appropriate Approach For Assay Validation In Cell & Gene Therapies

Explore the immense potential of gamma delta T cells, as well as the challenges in sourcing and scaling up sufficient volumes to treat enough patients.

#2. Daring To Learn From Failure: Insights On The Future Of Stem Cell Therapy

Examine the evolution of CAR T-cell therapy, its expanding role in earlier cancer treatment, challenges in applying it to solid tumors, and the future potential of generating CAR T-cells directly within patients. We highlight key scientific advancements, ongoing research, and the importance of learning from failures to drive innovation in stem cell therapy.

#3. Quintessential Role Of Apheresis In Gene-Modified T-Cell Therapy

Discover the critical role of leukapheresis in gene-modified T-cell therapy manufacturing. Learn how factors like anticoagulation, extracorporeal volume, and patient preparation impact collection efficiency. Explore best practices for optimizing donor eligibility, ensuring regulatory compliance, and standardizing processes to enhance the safety, consistency, and effectiveness of cell therapies.

#4. Host Cell DNA Impurities: A Unique Challenge For rAAV

Delve into the challenges of host cell DNA (hcDNA) impurities in recombinant AAV (rAAV) gene therapy. Nic Preyat at of UCB Pharma discusses potential risks, current limitations in purification, and the evolving regulatory landscape. Learn how process development strategies, from upstream cell line selection to downstream purification, can help mitigate hcDNA while maintaining product yield and safety.

#5. January 2025 — CDMO Opportunities And Threats Report

This report identifies CDMOs that might be impacted by key events affecting their clients, including company acquisitions, product acquisitions and licenses, product approvals, late clinical product terminations, and FDA rejections.

#6. New Reference Standards To Support Quality of AAV Raw And Starting Materials

US Pharmacopeia is developing reference standards to improve the quality of AAV gene therapy production. By standardizing raw materials like plasmid DNA and endonucleases, USP aims to enhance testing consistency, reduce impurities, and lower manufacturing costs, supporting the industry's growth.


“Understanding the delivery of genetic material to the heart using our delivery systems, making sure that we’re getting the right expression at the right doses … in a rare population is absolutely the right thing to do before we move over to more prevalent forms of heart disease.” Tenaya Therapeutics CEO, Faraz Ali

CELL & GENE LIVE! - Register Now


Register Now

Emerging Manufacturing Technologies For Cell Therapies

Thursday, March 13, 2025 11:00 AM Eastern Standard Time 1 hour

How can 3D cultures, organoids, & automation revolutionize cell therapy? Cell & Gene Live host, Erin Harris, welcomes experts Rohit Ingale of Arcellx & David O'Donnell from Vor Bio for an exploration of novel techniques to accelerate the development and production of transformative cell therapies! Don't miss this deep dive into the future of manufacturing! Registration is free thanks to the support of CPC and MaxCyte.


要查看或添加评论,请登录

Cell & Gene的更多文章