Serena De Vita, MD, PhD, on Speedy Manufacturing of PHE885 for Multiple Myeloma
The senior director and clinical program leader, Translational Clinical Oncology at Novartis Institutes for BioMedical Research, discussed new data from the phase 1 study.
“We're really striving to compress manufacturing timelines and to make sure that patients receive the cells as fast as possible and in the most reliable way possible... There's definitely an unmet need for patients we serve patients in the fourth or fifth line of multiple myeloma, they really have no options. Sometimes they progress very fast as they wait for the CAR T cells, so this definitely addresses a critical need for patients.”
Novartis’s PHE885 is an autologous BCMA-directed chimeric antigen receptor (CAR) T-cell therapy developed using the company’s T-Charge platform for the potential treatment of multiple myeloma. The therapy is being evaluated in a currently recruiting phase 1 study (NCT05172596).
Data from the phase 1 study were presented at the
CGTLive spoke with De Vita to learn more about the manufacturing advantages of the T-Charge platform and the data seen so far with PHE885. She discussed positive efficacy and safety data as well as another candidate developed with the T-Charge platform, YTB323.
REFERENCE
De Vita S. Clinical insights from PHE885, a Novel BCMA-directed CAR-T manufactured in < 2 days using the T-Charge platform. Presented at: OCTS USA 2022, June 29-30, Boston, MA.
Newsletter
Stay at the forefront of cutting-edge science with CGT—your direct line to expert insights, breakthrough data, and real-time coverage of the latest advancements in cell and gene therapy.
Related Articles
- ImmunoLogic, Episode 6: "The Future of Personalized Cancer Vaccines”
September 15th 2025
- Top News in Lymphoma Cell Therapy for World Lymphoma Awareness Day 2025
September 15th 2025
- Duchenne Action Month 2025: Looking Back at News and Expert Insights
September 14th 2025
- CGTLive®’s Weekly Rewind – September 12, 2025
September 12th 2025