ABOUT US

Introduction

Overview

Chongqing Precision Biotech Co., Ltd. was established in 2016 as a high-tech enterprise jointly established by a technical team with Professor Qian Cheng as the leader, a well-known scientist of precision medicine, and listed company, Zhifei Bio (Zhirui Investment). The company takes gene editing and synthetic Biotechtechnology as the breakthrough point, mainly engaged in the development and application of gene and cell medicine, and has become the leading enterprise in the field of CAR-T/NK in China. We determined to become a global, innovative and pioneering biopharmaceutical enterprise.

Adhering to the core concept of "keep improving and be meticulous", we focus on scientific research and continuously innovates. We have established R&D cooperation and expert exchange mechanisms with many overseas institutes and domestic universities, bringing together many experts and scholars and over 100 R&D elite team members. We set up an industrial technology research institute and a postdoctoral workstation, and have been approved as a new high-end research and development institution, key laboratory, engineering research center and other platform construction units in Chongqing.

As a scientific and technological innovation enterprise, the company grasps the key technologies in the field of cells, has a number of authorized invention patents and laid out patents in developed countries and regions. We has implemented and promoted more than 10 CAR-T R&D pipelines for leukemia, lymphoma, myeloma, gastrointestinal cancer, lung cancer, liver cancer, breast cancer and pancreatic cancer, and obtained implied licenses for four Class I CAR-T cell biological new drugs and ten indications. The first domestic self-developed pCAR-19B cell autologous infusion preparation for the treatment of childhood leukemia has been approved as "Breakthrough Therapy Designation" and included in the priority review. In 2024, NMPA has accepted our New Drug Application for pCAR-19B. Meanwhile, we has achieved technical breakthroughs in the treatment of renal cancer, colorectal cancer, gastric cancer and other solid tumors with CAR-T, and relevant products have been approved for clinical registration and are actively promoting clinical drug registration.

We have built an upstream and downstream integrated platform of 18,000-square-meter covering the development of cellular drugs, which can support the pre-clinical research, technological research and development, analytical testing and technological production of drugs IND and NDA. We are the first gene and cell pharmaceutical enterprise in western China and one of the few in China that has been granted CAR-T Pharmaceutical Production License. At the same time, we plans to build a regional cell preparation center in West Science City of Chongqing , covering an area of about 154 mu, with a planned total investment of 3 billion yuan.

We will continue to adhere to our mission of "innovation for health", make innovations for cell therapy technology and focus on malignant tumor treatment. Based on the domestic and international dual-cycle strategy, we will implement the strategy of globalization of technical resources and internationalization of marketing, build a regional cell preparation base in China, explore the establishment of overseas R&D branches, and strive to build a biomedical enterprise with global competitiveness.

Events
2015
2017
2018
2020
2021
2023
2024
New
2015
Sep.

The technical team signed a cooperation agreement with Zhirui Investment.

2016
Jan.

Chongqing Precision Biotech Co., Ltd. established.

Oct.

1st phase of 6,652 square meters R&D transformation base was started.

2017
May.

pCAR-19B product starts clinical IIT research.

2018
Feb.

pCAR-19B was accepted for clinical application of Class I New drugs.

Oct.

2nd phase of 15,700 square meters of R&D transformation base started construction.

2019
Feb.

The first indication of pCAR-19B was approved.

Oct.

The first case of dual-target CAR-T IIT study was enrolled.
CAR-T cell preparation workshop started.

Nov.

Start pCAR-19B registration clinical trial for children and adolescents with acute lymphoblastic leukemia.

Dec.

Start clinical lIT study of CEA target CAR-T in solid tumor projec.

2020
May.

Clinical implied license for two new indications of pCAR-19B was approved.

Oct.

Start the registered clinical trial of pCAR-19B cell therapy for adult (22-70 years old) B ALL.

Dec.

Class I New drug Clinical implied license of C-4-29 was approved.

2021
Jan.

The first IIT patient of CAR-NK was enrolled.

Mar.

The first IIT patient in CD19+CD22 dual-CAR-T project was enrolled.

May.

The first clinical patient with AML IIT was enrolled.
C-4-29 Clinical start-up; Phase I clinical start-up of MM indications.

Jun.

Signed an investment agreement with Chongqing Science City for the third phase of 100,000 ㎡ regional cell preparation base.

Jul.

C-13-60 solid tumor project IIT started.

Sep.

Complete phase I clinical of pCAR-19B ALL in children. C-4-29 RCC obtained clinical approval.

Dec.

Complete phase I clinical of pCAR-19B adult ALL.

2022
Feb.

Initiate Phase II registered clinical trial of pCAR-19B cell autotransfusion preparation for the treatment of children and adolescents with relapsed/refractory B-cell acute lymphoblastic leukemia (B-ALL).

Jun.

Chongqing Precision Biotech reported data from PrimeCAR-T platform at the American Society for Clinical Oncology (ASCO) Annual Meeting in 2022

Nov.

The number of our patent applications exceeded 100.

Dec.

Our self-developed C-13-60 cell preparation has been approved by NMPA for clinical trials

2023
Jan.

Approved Drug Production License for CAR-T cell therapy products

Jun.

Three abstracts of clinical and preclinical research results of Precision Biotech were published in ASCO official website.

Jul.

MC-1-50 received IND application acceptance by CDE.

Aug.

C-13-60 entered Phase I registration clinical trial.

Sep.

pCAR-19B phase II clinical trials for children's ALL was completed.

Oct.

The implied license of Class I biological new drugs for MC-1-50 was granted.

Nov.

pCAR-19B, as the first CAR-T product for the treatment of childhood leukemia in China was approved to be included in the list of "Breakthrough Therapy Varieties".

Dec.

MC-1-50 cell preparation and C-13-60 cell preparation were successively approved for the second indication.

2024
Jan.

The cell drug HVCT-RM traceability system of Precision Biotech was officially put into operation.

Jun.

pCAR-19B cell autologous infusion preparation (Priscabtagene Autoleucel Injection) was proposed to be included in the "Priority Evaluation Variety" for the treatment of CD19-positive relapsed or refractory B-cell acute lymphoblastic leukemia patients aged 3-21 years.

Jun.

Chongqing Precision Biotech announced its clinical breakthrough in solid tumors at the 2024 American Society of Clinical Oncology (ASCO) Annual Meeting .

Jul.

National Medical Products Administration (NMPA) has accepted the New Drug Application for our self-developed National Class I biological new drug pCAR-19B cell autologous infusion preparation (Priscabtagene Autoleucel Injection).

Technology Center of Enterprises of Chongqing

Chongqing High-tech Enterprise

Postdoctoral workstation

New high-end Research and Development Institution

Demonstration Alliance for Technological Innovation of Precision Medical Industry

Regional Cell Preparation Center

Chongqing Engineering Research Center for Genes and Cells

Chongqing Cell Therapy Engineering Research Center

Chongqing Key Laboratory of Gene and Cell Therapy

Chongqing Key Laboratory of Industry and Information Technology for Tumor Immunotherapy

Chongqing Cell and Gene Technology Innovation Center