According to a new research report “Global T-Cell Immunotherapy Pipeline Analysis, 2016 – Clinical Trials & Results, Patent, Designation, Collaboration, and Other Developments” published by P&S Market Research, the T cell immunotherapy exhibits strong pipeline with estimated 139 drug candidates in 2016.
T-cell immunotherapy pipeline in 2016
The study analyzed that the T-cell immunotherapy pipeline comprised of 139 therapeutic candidates, of which 16 are in Phase II stage of development. The high prevalence of cancer across the globe fuels the extensive research and development for the T-cell immunotherapeutic. T-cell immunotherapy is emerging as novel and promising approach for the treatment of cancer. It is gaining huge traction globally, for its several advantages over conventional therapies such as very low or no side effects and high specificity.
Browse the Report Summary at: https://www.psmarketresearch.com/market-analysis/t-cell-immunotherapy-pipeline-analysis
Insights on pipeline segments
As per the findings of research, it was found that around 22% T-cell immunotherapeutic candidate target CD19, and 6% target Prostate Specific Membrane Antigen (PSMA) and Prostate Stem Cell Antigen(PSCA). Around 62% pipeline therapeutic candidates of T-cell immunotherapy are being administered by intravenous route, 19% drugs are administered by parenteral route, 15% therapeutic candidates are administered by infusion route.
Chimeric antigen receptors (CAR) T-cell is majorly researched and developed, representing 75% T-cell immunotherapeutic candidates
CAR T-cells are the modified T-cells used to express CARs, which recognize specific antigens present on targeted cell. CARs are specifically designed synthetic receptors, linked with the single-chain variable fragment (scFV) of a monoclonal antibody. The domain includes T-cell receptor CD3-zeta chain, which graft specificity into an immune effector cell. It mediates T-cell cytotoxicity and activation when bound to a target cell.
Phase II, highest stage of development for T-cell immunotherapy
A total of 16 products are in Phase II stage, of which KTE-C19, anti-CD19 CAR T therapy of Kite Pharmaceuticals initiated to enroll submission of Biologics License Application (BLA) to the U.S. Food and Drug Administration (FDA) for the treatment of patients with relapsed/refractory aggressive B-cell non-Hodgkin lymphoma. Tisagenlecleucel-T, also known as CTL019 CART-19, is under Phase II stage of development by Novartis Pharmaceuticals for the treatment of acute lymphoblastic leukemia, chronic lymphocytic leukemia, diffuse large B cell lymphoma and non-Hodgkin’s lymphoma. U.S. FDA granted breakthrough therapy designation to CTL019 for the treatment of pediatric and adult patients with relapsed/refractory acute lymphoblastic leukemia in July 2014. The breakthrough therapy filing was submitted by the University of Pennsylvania’s Perelman School of Medicine, which has an exclusive global agreement with Novartis to research, develop and commercialize personalized CAR T-cell therapies for the treatment of cancers.
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Strategic collaborations for the development of T-cell immunotherapeutic
The research finds that the different companies are collaborating for the development of T-cell immunotherapeutic. In June 2015, Celgene Corporation and Juno Therapeutics, Inc. collaborated for the development and commercialization of immunotherapies. The two companies will leverage T-cell therapeutic strategies to develop treatments for patients with cancer and autoimmune diseases with an initial focus on CAR T and TCR technologies. Some of the key players developing T-cell immunotherapies are Novartis AG, Cellular Biomedicine Group, Inc., Kite Pharmaceuticals Inc., Juno Therapeutics, Inc., Gradalis, Inc., Atara Biotherapeutics, Inc., Adaptimmune Therapeutics Plc., Immunocore Limited, and Lion Biotechnologies, Inc.
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