About Us

Innovation Driven and Patient Centered

Suzhou Puhe Biopharma Co., Ltd.

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.

2021 2021

Year of establishment

200 200 +

Number of patent applications

14 14 +

Patents Granted

5 5 +

Preclinical Product Pipeline

4 4 +

Clinical Product Pipeline

Development History
2021

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

2022

PH001 received CDE Breakthrough Therapy Designation (BTD)

2023

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

2024

PH009 received CDE Phase I clinical trial approval, and the first patient was enrolled

2025

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)

Company Layout
Based in China, Embracing the World
Activated In progress
Beijing
Beijing

Operation Center
Project Management Center

Suzhou
Suzhou

R&D Center
Innovative Preparation Production Center

Henan
Henan

API Production Base
Topical Preparation Production Base

Shanghai
Shanghai

Business Development/Clinical
Innovation Platform

California
California

Overseas Clinical/Business Development
Innovation Platform

New York
New York

Overseas Clinical/Business Development
Innovation Platform

Beijing Suzhou Henan Shanghai California New York
Beijing

Operation Center
Project Management Center

Suzhou

R&D Center
Innovative Preparation Production Center

Henan

API Production Base
Topical Preparation Production Base

Shanghai

Business Development/Clinical
Innovation Platform

US East

Overseas Clinical/Business Development
Innovation Platform

New York

Overseas Clinical/Business Development
Innovation Platform