Suzhou Puhe Biopharma Co., Ltd. was founded in April 2021, jointly incubated by a well-known domestic pharmaceutical enterprise and the pharmaceutical industry fund "Shiyu Investment". We focus on the development of small-molecule innovative drugs for oncology, immunological disorders, and metabolic diseases, and are committed to becoming a leading BioPharma company rooted in China and oriented toward the global market.
Guided by a strategy of addressing differentiated clinical needs, we prioritize cancers with high incidence and mortality rates, such as lung cancer, pancreatic cancer, and gastrointestinal cancers, as well as areas with high clinically unmet needs including immunological disorders and metabolic diseases. With a comprehensive layout guided by scientific and industrial thinking, we actively explore R&D opportunities for innovative small-molecule drugs through independent research and in-licensing, and integrate resources to accelerate the company’s industrialization drive.
We have built a distinctive innovative small-molecule drug discovery and development platform by anchoring to molecular targets and integrating AI technology, with development capabilities to cover the entire development spectrum, including target discovery, molecular structure design, preclinical drug development, regulatory filing, clinical trial execution, and product manufacturing. Our pipeline spans multiple high-barrier development areas, such as next-generation kinase inhibitors, allosteric inhibitors, synthetic lethality, PROTACs, and molecular glues. Several drug candidates are in the global first tier in terms of development progress, with superior molecular properties and strong international competitiveness.
Year of establishment
Number of patent applications
Patents Granted
Preclinical Product Pipeline
Clinical Product Pipeline
Company was founded
In-licensed PH001
PH001 clinical phase I investigator meeting launched and the first EGFR exon20ins patient was enrolled
Established an R&D team and initiated independent research programs
PH001 received CDE Breakthrough Therapy Designation (BTD)
PH001 received CDE Phase III clinical trial approval, and the first patient was enrolled
PH001 was selected for poster discussion at ASCO
PH009 was selected for poster discussion at AACR
PH020 was selected for oral presentation at AACR
PH009 received CDE Phase I clinical trial approval, and the first patient was enrolled
The global exclusive rights of PH020 were licensed to Bayer
Bayer initiated the global multicenter Phase I clinical trial of PH020 and completed the first patient enrollment
Angel round of financing led by YuanSheng Venture Capital was completed
PH027 received IND approval from the CDE (NMPA)
Operation Center
Project Management Center
R&D Center
Innovative Preparation Production Center
API Production Base
Topical Preparation Production Base
Business Development/Clinical
Innovation Platform
Overseas Clinical/Business Development
Innovation Platform
Overseas Clinical/Business Development
Innovation Platform
Operation Center
Project Management Center
R&D Center
Innovative Preparation Production Center
API Production Base
Topical Preparation Production Base
Business Development/Clinical
Innovation Platform
Overseas Clinical/Business Development
Innovation Platform
Overseas Clinical/Business Development
Innovation Platform