Enteropathy-associated T-cell lymphoma

Corvus Pharmaceuticals Announces Publication of Preclinical Data Demonstrating Potential of ITK Inhibition with Soquelitinib as a Novel Approach to T Cell-Mediated Inflammatory and Immune Diseases

Retrieved on: 
Wednesday, November 1, 2023

BURLINGAME, Calif., Nov. 01, 2023 (GLOBE NEWSWIRE) -- Corvus Pharmaceuticals, Inc. (Nasdaq: CRVS), a clinical-stage biopharmaceutical company, today announced the publication of preclinical data that demonstrated the potential of ITK inhibition as a novel approach to treat T cell-mediated inflammatory and immune diseases. Corvus’ ITK inhibitors include soquelitinib (formerly known as CPI-818), which was used in the preclinical studies and is currently in clinical trials for oncology indications, and several next-generation molecules that are being optimized for use in a variety of inflammatory and immune disease indications.

Key Points: 
  • “Our research on soquelitinib and selective ITK inhibition is uncovering valuable new information about immune function and the role of ITK in different diseases,” said James Rosenbaum, M.D., senior vice president of research at Corvus.
  • “The activity of soquelitinib in various inflammatory and immune disease models highlights the essential role of ITK in multiple T cell functions.
  • The publication is now available online as a preprint at bioRxiv.org and on the Publications and Presentations page of the Corvus website.
  • With this new publication, we further demonstrate the wide range of opportunities for ITK inhibition across specific indications with ongoing patient needs for new therapies.

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

Retrieved on: 
Thursday, August 6, 2020

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.

Key Points: 
  • 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.
  • The trials enrolled 41 adult patients with relapsed/refractory Hodgkin Lymphoma who received CD30 CAR-T cell therapy following lymphodepletion with chemotherapy.
  • 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 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

Retrieved on: 
Thursday, August 6, 2020

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.

Key Points: 
  • 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.
  • The trials enrolled 41 adult patients with relapsed/refractory Hodgkin Lymphoma who received CD30 CAR-T cell therapy following lymphodepletion with chemotherapy.
  • 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.