About Us
Focus on the early discovery and clinical development of bispecific antibody and ADC.
since
2023
Shanghai Allink Biotherapeutics Co., Ltd.

Founded in 2023, Allink Biotherapeutics transcends traditional treatment limitations through breakthrough bispecific antibodies and ADC therapeutics. Our interdisciplinary teams unite rigorous scientific methodology with unwavering patient-centered purpose, transforming complex clinical challenges into hope-inspiring therapeutic solutions.
Our Technology Platforms and Pipeline
Bispecific Antibody Platform — Exploring new frontiers in precision-targeted therapy through collaborative innovation
• ADC Technology Platform — Engineering high DAR, enhanced hydrophilicity and diverse configurations for next-generation ADC
• Diversified Pipeline — Building First-in-Class and Best-in-Class candidates across oncology and immune diseases
Our commitment to translating scientific potential into clinical impact is demonstrated through two ADC programs advancing to global Phase I trials - a pivotal milestone where collaborative excellence meets meaningful patient care. Multiple early-stage programs have achieved pipeline candidacy, establishing our foundation for sustained therapeutic development and global impact.
Headquartered in Shanghai's Pudong New Area (4560 Jinke Road), we operate with worldwide perspective while remaining rooted in collaborative scientific discovery.

Allink was established in 2023

Over 5 patents covering products and technology

Nearly 30 years of experience in biopharmaceutical and ADC R&D

More than 10 innovative pipelines

Core competitiveness

Experienced R&D team

Efficient execution

Proprietary platform

International collaboration experience

Experienced Leadership Team

AllinkBio's leadership team brings over 20 years of extensive expertise in innovative drug development and corporate growth

Hui FENG Ph.D.

Hui FENG Ph.D.

Founder / CEO

Dr. Feng brings nearly two decades of distinguished leadership in biopharmaceutical development and portfolio strategy. His career is defined by breakthrough achievements, including leading the development of China's first overseas -approved PD-1 monoclonal antibody (Toripalimab). During the COVID-19 pandemic, he spearheaded collaborative development of a neutralizing antibody that achieved emergency use authorization across 17 countries, directly contributing to global pandemic response efforts

Kehua FAN EMBA

Kehua FAN EMBA

Co-founder / COO

Dr. Fan brings nearly two decades of expertise in global business development and clinical development within pharmaceutical industry.She has closed over 15 multinational licensing deals in her career, including the landmark out - licensing of a COVID-19 neutralizing antibody to Eli Lilly that generated $425+ million in revenue. Her strategic leadership in international partnerships consistently accelerates drug development while maximizing both scientific innovation and commercial value creation

Li LI Ph.D.

Li LI Ph.D.

Co-founder / Head of Research

Dr. Li has over a decade of specialized expertise in bispecific antibody (BsAb) and antibody-drug conjugate (ADC) development ,currently leading early-stage program research. He has led and participated in 5 innovative therapeutic programs supported by NSFC funding ,filed over 10 patent applications for novel therapeutic antibodies. Dr. Li played a critical role in the preclinical development of Etesevimab, a COVID-19 neutralizing antibody that received global emergency use authorization

Xiaolin WANG

Xiaolin WANG

Head of Clinical Research

Xiaolin is a seasoned clinical development leader with over 18 years of comprehensive experience spanning oncology, immunology, respiratory diseases, and multiple therapeutic area.She brings extensive expertise in clinical development that accelerate therapeutic development from early-phase studies through regulatory approval. She has successfully led more than 15 clinical trials across global markets, demonstrating exceptional expertise in managing complex, multi-site international studies.

Jun WANG.Ph.D.

Jun WANG.Ph.D.

Head of ADC Platform Development

Dr. Wang delivers over two decades of distinguished leadership in biologics research and antibody-drug conjugate (ADC) development.He earned his Ph.D. in Chemistry from Columbia University and currently overseeing ADC and small molecule platform development. Dr. Wang has demonstrated exceptional expertise in advancing therapeutic candidates from research through clinical stages. His strategic leadership has been instrumental in establishing technology platforms and research team management.

Echo Chen, ACCA

Echo Chen, ACCA

Head of Finance

With over two decades of financial and operational leadership in the pharmaceutical industry, Echo brings comprehensive expertise from senior roles at multiple MNCs and large pharmaceutical companies. Her strategic leadership encompasses establishing robust financial controls and compliance frameworks, driving operational process innovations, and delivering data-driven business insights that consistently enhance investment effectiveness and operational efficiency, enabling scalable enterprise development.

Corporate Culture
Mission
Mission

Through continuous scientific innovation, we are committed to developing world-class bispecific antibodies and ADC drugs to address unmet medical needs globally

Vision
Vision

To innovate and develop cutting-edge products that enhance human health and well-being, while adhering to the highest standards of scientific excellence.

Values
Values

Innovation-driven, patient-centered and proactively collaborative.

Development Path
2023

Successfully secured $23.5 million in Angel Fund investment, establishing robust financial infrastructure to accelerate therapeutic platform development and clinical advancement initiatives.

2024

In November, we achieved dual milestones with our $42 million Series A financing closure and FDA IND approval for ALK201.

2025

In March, we achieved a transformative milestone with ALK202 receiving CDE IND approval and successfully completing first patient enrollment in global Phase I trial.

2023
2024
2025