about

The goal is to to bring more affordable,high-quality biologic medicines to patients.

Our leading pipeline is a next generation of anti-IgE antibody (LP-003), which is already in Phase III stage, and prepare for BLA in 2026. The other pipeline is a bifunctional complement inhibitor (LP-005) , which is in Phase II at present.

Research progress
Development
course
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Dr. Sun, Bill Nai-chau
Dr. Sun, Bill Nai-chau

Dr. Sun, is one of the serial successful entrepreneurs in the

biopharmaceutical industry with proven track records of successful biopharmaceutical

development in both China and the United States. Dr. Sun was a shareholder of Tanox Inc., a

biotech company established in Texas, the United States in 1986 and listed on the NASDAQ

Stock Market in 2000. He co-founded PharMab Inc. in 2001 and our Company in 2020. Dr. Sun

obtained a Ph.D. in cell biology from the Iowa State University in the United States and has

over 55 years of experience in biomedical research and development. He has published more

than 30 research papers in leading chemistry and medicinal chemistry journals and has been

granted 30 patents, including 16 registered in the United States and 12 patents registered in the

PRC. He was the main inventor behind the groundbreaking first-generation anti-IgE antibody,

omalizumab (marketed as Xolair®), which emerged as a blockbuster in asthma and allergic

diseases, and F-627/long-acting G-CSF (marketed as Benegrastim, Ryzneuta®). Dr. Sun’s

industry insights and vision are crucial to our continuous innovation. 

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Dr. Liu, Heng

Dr. Liu, our co-founder, has over 15 years of experience in research and

development and commercialization of biopharmaceutical drugs. Dr. Liu played a pivotal role

in both domestic and international programs of development of several innovative drugs.

Notably, Dr. Liu was deeply involved in the development of a long-acting G-CSF (marketed

as Ryzneuta®), which successfully completed phase III clinical trials globally and received

market approval from the Food and Drug Administration in the United States and the NMPA.