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Thursday, August 06 2020 - 22:11
AsiaNet
Tessa Therapeutics Announces Results from Two Independent Phase 1/2 Trials of Autologous CD30 CAR-T Cell Therapy in Patients with Relapsed or Refractory Hodgkin Lymphoma
SINGAPORE, Aug. 6, 2020 /PRNewswire-AsiaNet/ --

Tessa Therapeutics (Tessa), a clinical-stage cell therapy company developing 
next-generation cancer treatments, today announced the publication of results 
in the Journal of Clinical 
Oncology(https://ascopubs.org/doi/abs/10.1200/JCO.20.01342?journalCode=jco) 
from two investigator-sponsored Phase 1/2 trials led by Baylor College of 
Medicine and the University of North Carolina Lineberger Comprehensive Cancer 
Center. 

Results of the trials, which evaluated the safety and efficacy of CD30 CAR-T 
cell therapy in patients with relapsed/refractory ("R/R") Hodgkin lymphoma, 
showed a high rate of durable complete responses and very favorable safety 
profile using autologous CD30 CAR-T cell therapy. 

"These data are significant, as they demonstrate that CAR-T cell therapy may be 
a safe and effective treatment option for patients with Hodgkin lymphoma and 
potentially other lymphomas expressing the CD30 antigen," said Dr. Natalie 
Grover, study co-first author, assistant professor in the UNC Department of 
Medicine and a UNC Lineberger member. "The highest dose treatment led to the 
complete disappearance of tumors in the majority of patients, and almost all 
subjects had clinical benefit. As such, we believe further study of this 
treatment approach is warranted," said Dr. Carlos Ramos, study co-first author, 
professor at the Center for Cell and Gene Therapy at Baylor College of 
Medicine, Houston Methodist Hospital and Texas Children's Hospital.

The trials enrolled 41 adult patients with relapsed/refractory Hodgkin Lymphoma 
who received CD30 CAR-T cell therapy following lymphodepletion with 
chemotherapy. Overall, 94 percent of the treated patients were still alive a 
year after treatment. Of the patients who had a complete response, 61 percent 
still had no evidence of recurrence a year later. None of the patients 
experienced the serious, life-threatening complications that have been seen 
with several CD19 CAR-T cell trials. The overall response rate in the 32 
patients with active disease who received fludarabine-based lymphodepletion was 
72%, including 19 patients (59%) with complete response.

"We have been working with Baylor and the University of North Carolina to 
confirm these impressive results further in a Tessa-sponsored regulatory Phase 
2 trial, which we aim to initiate this year," said Ivan D. Horak, M.D., 
President of Research and Development at Tessa Therapeutics. "Longer term, we 
seek to explore the potential of this therapy beyond Hodgkin's lymphoma to 
CD30+ expressing Non-Hodgkin lymphomas, where there is a demonstrated unmet 
need."

University of North Carolina has granted Tessa an exclusive license to its 
patents, data and know-how, and Baylor College of Medicine has granted Tessa 
the rights to use its data and know-how, for the further development and 
commercialization of this therapy. "We are excited to collaborate with Tessa. 
Their ability to run multi-center cell therapy clinical trials will be 
invaluable for the further development of this therapy," said Helen Heslop, 
director of the Center for Cell and Gene Therapy and Dan L Duncan Chair at 
Baylor. 

About Tessa Therapeutics 

Tessa Therapeutics is a clinical-stage biotechnology company focused on the 
development of cell therapies for a broad range of cancers. 

Tessa's clinical pipeline derives from two innovative cell therapy platforms: 
CD30 Chimeric Antigen Receptors (CD30-CARs) and Virus-Specific T cells (VSTs). 
Our lead candidate comprises autologous CD30 CAR-T cell therapy targeting 
classical Hodgkin lymphoma (cHL) and CD30+ non-Hodgkin lymphomas. 

Tessa, in collaboration with Baylor College of Medicine, is also developing a 
novel, allogeneic platform technology, as a new approach to traditional cell 
therapy. By combining the unique properties CD30-CARs and VSTs, the platform 
holds potential for the creation of next-generation off-the-shelf cell 
therapies against a variety of hematologic malignancies and solid tumors.

Tessa's state-of-the-art GMP cell therapy manufacturing facility will open in 
early 2021 and will substantially enhance in-house production capabilities. 
Tessa is focused on rapidly and reliably providing safe, effective treatment 
options for patients.

For more information on Tessa, please visit www.tessatherapeutics.com. 

Source Tessa Therapeutics