PLEASANTON, CALIF., NANJING, CHINA, May 21, 2021 - IASO Biotherapeutics announces today that its clinical trial application for the in-house developed CD19-CD22 fully human dual-targeted CAR T-cell therapy (CT120) for the treatment of its second indication, relapsed/refractory B-cell non-Hodgkin's lymphoma (B-NHL), has been accepted by National Medical Products Administration (NMPA) (Acceptance No.: CXSL2101088, CXSL2101089). This acceptance comes only one day after the acceptance of the drug’s first indication for the treatment of CD19/CD22 positive relapsed/refractory B-cell acute lymphoblastic leukemia (B-ALL). This success in clinical trial application further highlights the company’s speed of and strength in the development of innovative novel CAR-T therapies.
CT120 is developed on the company’s fully human antibody platform IMARS and high throughput CAR-T drug selection platform. IMARS antibody discovery platform is among the top ones in the industry in terms of database capacity - over 240 billion candidate antibodies render the platform powerful capacity and fast speed of antibody screening., The company’s high through-put CAR-T drug selection platform that makes use of cutting edge single-cell analysis and next-generation sequencing (NGS) technology is capable of implementing cost effective, high efficiency functional CAR-T candidate screening. CT120 is prepared at company’s integrated in-house good manufacturing practice (GMP) compliant manufacturing facility in Nanjing, which is fully equipped to produce high quality plasmids, viral vectors and gene edited cellular products in a cost-efficient manner.
B-cell non-Hodgkin's lymphoma (B-NHL) is a group of hematologic malignancies of B-lymphocytes origin. Current standard of care (SOC)include chemotherapy, radiotherapy, hematopoietic stem cell transplant, molecular targeted drug, etc.Most patients can achieve short-term remission after the administration of standard of care, however, relapsed or refractory disease are frequent in some patients. For such patients, conventional therapies are limited and CAR-T therapy is considered to be one of the most promising ones. CD19-targeted single-targeted CAR-T therapy has shown good efficacy in clinical studies, but some patients would still experience progression or recurrence with a short time after CD19 CAR-T therapy (ref). CD19 antigen escape on the surface of tumor cells is thought to be one of the possible mechanisms.
It has been shown in studies that both CD22 and CD19 are generally expressed on the surface of multiple B-cell tumors, including B-NHL. Similar to CD19, CD22 is also expressed ontumor with certain specificity, which makes it another ideal therapeutic target. In light of this, CD19 and CD22 dual-targeted CAR-T therapy theoretically can reduce the risk of treatment evasion as a result of the missing of a single target and show the prospect for further reducing disease recurrence, yielding long-term survival benefit for patients.
“The Investigator initiated trials (IITs) underway in Tongji Hospital Affiliated to Tongji Medical College of Huazhong University of Science & Technology and the First Affiliated Hospital, College of Medicine, Zhejiang University showed the fully human dual-targeted CT120 not only benefits CAR-T naïve relapsed/refractory B-ALL patients but also benefits patients whose disease progressed during or after murine single-targeted CD19 CAR-T. Therefore, the therapy is of promising prospect in terms of both market landscape and patient benefits. More importantly, the submission of IND for this product marks the maturation of the company’s phage antibody library-based antibody discovery platform. It is expected that fully human antibody products based on this antibody library will continuously contribute to the company’s cell therapy and antibody therapy pipelines. In IASO Biotherapeutics, we will continue to expand and exploit new product pipelines to benefit more patients in the future.” Dr. Wang Wen, CEO, IASO Biotherapeutics.
