About YZYBIO
A biotechnology company dedicated to developing BsAb-based therapies to treat
cancer or cancer-associated complications and age-related ophthalmologic diseases
Company Overview
Wuhan YZY Biopharma Co., Ltd.

WUHAN YZY BIOPHARMA CO., LTD. was established in 2010 and is a biotechnology company dedicated to the development of bispecific antibody (BsAb) therapies. The Company focuses on therapeutic areas with significant market potential, including oncology and its complications, age-related ophthalmologic diseases and autoimmune diseases, and has proactively established proprietary innovative technology platforms, including YBODY®, Check-BODY and Nano- YBODY®. Leveraging its strong research and development capabilities, the Company has established a pipeline of multiple drug candidates, including its core product M701, of which four are currently at the clinical development stage and two are at the preclinical research stage.

 

With respect to its core product, M701, a bispecific antibody targeting EpCAM/CD3 independently developed by the Company, has made significant clinical progress. To date, the new drug application (NDA) for M701 for the treatment of malignant ascites has been accepted by the China National Medical Products Administration, while the investigational new drug (IND) application for M701 for the treatment of malignant pleural effusion has been approved by the U.S. Food and Drug Administration (FDA). In addition, data from two important clinical studies of M701 were selected for presentation at the 2026 Annual Meeting of the American Society of Clinical Oncology (ASCO), further validating the clinical value and international potential of the product.

 

The Company continues to deepen its external technology collaborations. By entering into licensing cooperation agreements with leading companies in the industry, the Company has steadily advanced its research and development services and milestone recognition, effectively optimising its research and development expenditure structure. The Company will continue to uphold its mission of “discover and develop innovative drugs to improve the health and well-being of patients”, accelerate the commercialisation of its core pipeline and strive to provide high-quality innovative treatment solutions to patients worldwide.

  • 4
    Innovative Platforms
  • 80 %
    R&D Employees
  • 78
    Patents and patent applications
    (of which 33 have been issued, and 45 applications are pending)
Leadership Team
Chairman of the Board & Chief Executive Officer
Dr. Zhou Pengfei
Dr. Zhou PengfeiChairman of the Board & Chief Executive Officer

Dr. Zhou Pengfei, the co-founder of the Group, was appointed as a director and the chief executive officer of the Company. He is responsible for the overall strategic. Dr. Zhou obtained a bachelor’s degree in pediatrics in June 1989, and a master’s degree in pediatric surgery (oncology) in June 1994, from Tongji Medical University (同济医科大学) respectively.He also got a Doctor of Philosophy from McMaster University in November 2005.

Dr. Zhou has over 30 years of experience in the healthcare and pharmaceutical industries, he worked for a number of leading enterprise, including Schering-Plough Corporation, Crown Bioscience International, acquired unique expertise in tumor biology and tumor immunotherapy.

Dr. Zhou now has served as a visiting professor at Tongji Medical College of Huazhong University of Science and Technology as well as a visiting professor at Central South University.

Vice President of Research & Development
Dr. Yang Bin
Dr. Yang BinVice President of Research & Development

Dr. Yang Bin currently serves as the vice president of the manufacturing center of the Company, who is responsible for implementing the Group’s strategies and goals for technology development and product manufacturing. Dr. Yang obtained a bachelor’s degree in pharmacy from Wuhan University and obtained PhD in biomedicine from Jinan University (暨南大学).

Prior to joining YZY Biopharma, Dr. Yang served in various key positions at Shenzhen HEC Industrial Development Co., Ltd. and its subsidiaries (“HEC Group”), including the head of the monoclonal antibody department and deputy director of the biopharmaceuticals research institute.

  • Dr. Zhou Pengfei, the co-founder of the Group, was appointed as a director and the chief executive officer of the Company. He is responsible for the overall strategic. Dr. Zhou obtained a bachelor’s degree in pediatrics in June 1989, and a master’s degree in pediatric surgery (oncology) in June 1994, from Tongji Medical University (同济医科大学) respectively.He also got a Doctor of Philosophy from McMaster University in November 2005.

    Dr. Zhou has over 30 years of experience in the healthcare and pharmaceutical industries, he worked for a number of leading enterprise, including Schering-Plough Corporation, Crown Bioscience International, acquired unique expertise in tumor biology and tumor immunotherapy.

    Dr. Zhou now has served as a visiting professor at Tongji Medical College of Huazhong University of Science and Technology as well as a visiting professor at Central South University.

  • Dr. Yang Bin currently serves as the vice president of the manufacturing center of the Company, who is responsible for implementing the Group’s strategies and goals for technology development and product manufacturing. Dr. Yang obtained a bachelor’s degree in pharmacy from Wuhan University and obtained PhD in biomedicine from Jinan University (暨南大学).

    Prior to joining YZY Biopharma, Dr. Yang served in various key positions at Shenzhen HEC Industrial Development Co., Ltd. and its subsidiaries (“HEC Group”), including the head of the monoclonal antibody department and deputy director of the biopharmaceuticals research institute.

Milestones
2010
July

The predecessor of the Company, Wuhan YZY Biopharma Limited Company was established.

The initiation of BsAb platform development

2012
May
Established a GMP-compliant quality system
November

The initiation of M802 R&D

The filing of the PCT patent application “Bispecific antibody” for the protection of the YBODY® platform

2013
July
The initiation of M701 R&D
December
The determination of molecule structure of M802 and M701
2014
June
Novel Bispecific Antibody Drugs for the Treatment of Tumors Development Project (“新型肿瘤治疗性双特异性抗体药物开发课题”) selected for the Major Science and Technology Special Project for “Significant New Drugs Development” (“重大新药创制”科技重大专项) under the Twelfth Five-year Plan.
2015
September
M701 selected for the Major Science and Technology Special Project for “Significant New Drugs Development” (“重大新药创制”科技重大专项) under the Twelfth Five-year Plan.
2016
April
M802 became the first BsAb to file IND application in China.
August
Completed Series Pre-A Financing(1) and raised an aggregate amount of approximately RMB50 million.
2017
February

Patent protection for our YBODY® platform in U.S. expanded to cover 35 targets.

M701 became the second BsAb to file IND application in China.

September
Obtained NMPA IND approval for the clinical investigation of M802 in China, which is China’s first IND approval for self- developed BsAb.
2018
February

M701 received China’s second IND approval for self-developed bispecific antibody.

March 2018 The establishment of the Check-BODY platform

March
The establishment of the Check-BODY platform
April
Completed Series A Financing(1) and raised an aggregate amount of approximately RMB157.2 million.
December

Patent issued for the protection of M802 in China.

Patent issued for the protection of our YBODY® platform in CD3 and HER2 targets in U.S.

The establishment of the Nano-YBODY™ platform

2019
July
PCT patent application for the protection of our Check-BODY Platform was filed.
August
Obtained FDA IND approval for the clinical investigation of M802 in U.S.
October
Obtained FDA IND approval for the clinical investigation of M701 in U.S.
2020
February
The establishment of the UVAX® platform
August
Obtained FDA IND approval for the clinical investigation of Y150 in U.S.
2021
January

Completed Series B Financing(1) and raised an aggregate amount of approximately RMB168.7 million.

Obtained NMPA IND approval for our clinical investigation of Y150 in rrMM in China.

Obtained FDA IND approval for our clinical investigation of Y101D for solid tumors in U.S.

February
Completed Series B+ Financing(1) and raised an aggregate amount of approximately RMB20 million.
May
Obtained NMPA IND approval for our clinical investigation of Y101D in metastatic or locally advanced solid tumors in China.
August
Completed Series B++ Financing(1) and raised an aggregate amount of approximately RMB73.5 million.
December

Obtained NMPA IND approval for our clinical investigation of Y2019 in China

Initiated a Phase II clinical trial for M701 monotherapy in combination with systematic treatment for MA in patients with EpCAM-positive carcinomas in China.


2022
January

The Company was converted into a joint stock limited company with its name changed to “Wuhan YZY Biopharma Co., Ltd.(武汉友芝友生物制药股份有限公司)

July

Obtained IND approval for a Phase Ib/II clinical trial of M701 for the treatment of MPE in China.

Entered into asset transfer agreement with CMS Vision for Y400.

October
Completed Series C Financing(1) and raised an aggregate amount of approximately RMB200 million.
December

Obtained the IND approval for a Phase Ib/II clinical trial of Y101D in combination with gemcitabine and albumin paclitaxel as the first-line treatment for pancreatic cancer patients in China

Obtained IND approval for a Phase Ib/II clinical trial of Y101D in combination with bevacizumab in treating HCC and other advanced solid tumors in China

2023
April

Y332 received Investigational New Drug (IND) approval from the China National Medical Products Administration (NMPA)

Y400 received Investigational New Drug (IND) approval from the China National Medical Products Administration (NMPA)

September
Was listed on the Main Board of HKEX. Stock:2496
October
Completed enrollment for the Y101D Phase II clinical trial for pancreatic cancer
November
Obtained recognition as a High-tech Enterprise
December
Completed the M701MPE Phase Ib clinical trial
2024
March
March M701 was approved to proceed to Phase Ⅲ clinical trials for the treatment of malignant ascites
March
March M701 treatment for malignant pleural effusion advanced to Phase Ⅱ clinical trials
October
October A transaction worth a total of RMB 315 million was agreed upon with CHIATAI TIANQING for the domestic rights of M701
December
December The project on key technological innovation and clinical application of immunotherapy for non small cell lung cancer received the First Prize of the National Science and Technology Progress Award
2025
September
September Co-established Antibody Drug Development and Achievement Transformation Center with Hubei Jiangxia Laboratory
October
October Y225 obtained Chinese patent granted protection
October
October M701 Phase II interim study data presented at ESMO Congress 2025
November
December Y225 obtained NMPA IND approval in China
December
November M701 Phase II clinical results published in renowned international journal EHO
2010
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
Contact Us
  • Phone:
    027-82668988
  • E-Mail:
    info@yzybio.com
  • Postcode:
    430075
  • Address:
    Biolake, C2-1, No. 666 High-tech Avenue, Wuhan, Hubei, China
  • Fax:
    027-68788819
  • Business Development Contact:
    wangjing@yzybio.com chenling@yzybio.com