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Neukio Biotherapeutics on a New Mission

Corporate Overview

Neukio Biotherapeutics

Neukio (Shanghai) Biotherapeutics focuses on iPSC-derived CAR-NK/CAR-T technology platforms and next-generation off-the-shelf immune cell products for treating solid tumors and autoimmune diseases. While driving independent innovation, the company actively collaborates with leading global institutions to develop original, clinically valuable immune cell therapies, including iNK, iT, and in vivo CAR. These innovations aim to enhance efficacy while significantly reducing production costs, delivering safe and effective treatments to patients worldwide. 


Neukio was established in June 2021 in the Shanghai Waigaoqiao Free Trade Zone. In July of the same year, the company announced the completion of a $40 million Angel financing round led by Lilly Asia Ventures, along with Sherpa and IDG Capital. By December 2021, Neukio had completed the renovation of a 6,000-square-meter integrated R&D and manufacturing center in just six months. The facility includes a 1,000-square-meter R&D lab, 2,500 square meters of process development and GMP production cleanrooms, and QC labs,  supporting research and development end-to-end operations. In September 2022, Neukio secured $58 million in Series A financing led by CD Capital, with participation from Yahui Investment, Kuan Capital, Alibaba Health, and Panlin Capital, alongside continued support from the Angel investors. 


How does Neukio innovate? 

1: Leveraging the core team’s experience in bringing China’s first autologous CAR-T product to market, Neukio identified the limitations of autologous cell therapies and opted for iPSCs as an ideal seed cell source for off-the-shelf immune cell therapies. The company simultaneously advances CAR-NK and CAR-T technology platforms, positioning itself as one of the few biotechs globally pursuing dual-platform immune cell development. 

2: Utilizing iPSC clonality and ease for precision gene editing, Neukio modifies specific signaling pathways in iPSCs by knocking out genes or inserting functional transgenes including CAR gene at targeted genomic loci. This approach enhances product tumor killing and immune modulation properties to address challenges in solid tumor treatment, such as immunosuppressive microenvironments and poor tumor infiltration, and to target tumor specific antigens by encoded CAR molecule. The platform enables iterative editing and validation until optimal functional products are obtained—a process impossible with primary cells requiring multiple editing and clonal selection. 

3: Neukio establishes a robust three-tiered cell banking system from genomically edited, stable clones. The company has developed and validated a continuous 3D bioreactor suspension process with perfusion option for iPSC differentiation and expansion into iNK/iT cells. The unique feature of serum-free, feeder-free, GMP-compliant manufacturing system ensures high yield, purity, stability, and safety of homogeneous CAR-iNK/CAR-iT products, drastically reducing production costs while eliminating iPSC residues and tumorigenic risks—a breakthrough in industrial-scale manufacturing of iNK. Currently, Neukio has built a multi-target, multi-mechanism and multi-indication iNK pipeline with three candidates in clinical validation. The iT pipeline, focused on enhancing in vivo activation, expansion, and persistence, is under development, with lead candidates nearing preclinical testing. Building on its CAR-T/CAR-NK expertise, Neukio is also pioneering in vivo CAR technology as the ultimate goal of cell therapy development to benefit patients globally. 



Our Competitive Advantages


l  Dual iNK/iT technology platforms and pipelines

l  Extensive cell therapy industrialization expertise (gene editing, CAR-T, CMC, regulatory) 

l  Dual-strategy product development combining in-house R&D and external collaborations

l  Exceptional execution speed driven by highly efficient teamwork 

l  Strong support from visionary investors


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Development History

  • 2021

    June: Founded in China (Shanghai) Pilot Free Trade Zone

    July: Completed $40M angel round financing

    September: Discovery laboratory center construction completed

    December: GMP manufacturing facility construction completed

  • 2022

    January: Collaboration with Biocytogen to screen antibody for nominated targets for construct next generation of CAR cellular immunotherapy products

    February: Collaboration with EdiGene Inc. to explore novel therapeutic mechanisms and potential targets to be edited

    July: Achieved the first gene editing and functional validation

    July: Completed small scale manufacturing process

    November: Collaboration with ExCell to develop customized serum-free medium for NK cells and other iPSC derived products

  • 2023

    January: Completed GMP compliant 3-tier Banking (PCB/MCB/WCB) for manufacturing of clinical grade iNK

    May: Completed mid-scale production of iNK

    June: Closed Series A1 fundraising of $58M

    August: Initiated in vivo efficacy studies, and observed siginicant anti-tumor activity

    November: Accomplished toxicological studies for IIT

    December: Ranked as top 50 in "China Innovation and Entrepreneurship Competition”

  • 2024

    April: Completed the first GMP-compliant manufacturing of iNK cell products

    April: Awarded "Top 20 Innovative Enterpreneurship in Pudong New Area"

    April: Selected as "Shanghai Key Service Unicorn Potential Enterprise"

    May: Approved by China Society for Drug Regulation to undertake the research project "Development and Application of ddPCR technology in the CMC, Pre-clinical, and Clinical Evaluation of iPSC-Derived Cell Therpay Products"

    May:Initiated the first clinical study (IIT)

    July: Included in the public list of small and medium-sized innovative enterprises in Shanghai

    August: Included in the national small and medium-sized science and technology enterprise repository

    November:  Has been selected as one of six pilot companies in Shanghai to be exampted from the national ban on Foreign Invested Enterprise to conduct research and development of stem cell and gene diagnosis and therapeutic treatment

  • 2021

  • 2022

  • 2023

  • 2024

Corporate vision

Let Cell Therapies Eradicate Cancer Cells

Corporate mission

Focus on Innovative Technology and Therapy Development

Uphold High Quality Standards and Industry Leadership

Corporate value

Honesty and Integrity

Responsibility and Accountability

Respect and Collaboration

Result and Excellence

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About Founder

Richard Liqun Wang Ph. D., MBA.

Founder, Chairman and CEO, Neukio Biotherapeutics, developing next generation cell therapy via iPSC-CAR-NK and iPSC-CAR-T approach 


Former positions held:

  • Founding CEO, Fosun Kite Biotech

  • VP & CTO, Fosun Pharma

  • COO and General Manager, Cellular Biomedical Group

  • Head of Operations, GSK R&D Center in China

  • Director of Alliance, Externalization and Portfolio Management, AstraZeneca Innovation Center China

  • Associate Director, Discovery Portfolio and Project Management, Bristol-Myers Squibb, USA

  • Group Leader & Principal Scientist, P&G Pharmaceuticals, USA


Richard received B.S degree in Cell Biology from University of Science & Technology of China, Ph.D. in Molecular Biology from University of Maryland, Baltimore and MBA from Xavier University in Cincinnati. He obtained postdoctoral training at the National Institutes of Health, USA. Over the 30+ years of pharmaceutical research career, he led several drug discovery and translational programs leading to clinical trials. In the last 10 years, he has focused effort on cell therapy research and product development. While in Fosun Kite, he led the team to complete tech transfer, registration trial and market authorization application for Yescarta (first CAR-T product approved in China) in less than three years, and built commercial strategy and teams for the launch.


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Core Team

The core management team has rich experience in R&D, production and manufacturing of cell therapies.

40% previously worked in the management team of Fosun-Kite, and led Fosun-Kite to complete the technology transfer, facility construction, clinical trials, drug regulatory review and successful approval of Yescarta for commercialization in China.

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