ClinPlus provides site management services to both local and global companies in research development in pharmaceuticals, medical devices, and health-related products. Since its establishment in 2009, ClinPlus has been committed to undertaking clinically valued innovative drugs projects. It has participated in over 2100 SMO projects and has covered 24 medical units in total, including tumors, endocrine diseases, medical devices, viral hepatitis, immune diseases, blood diseases, infection and more. It has also brought into the market over 90 drugs domestically and worldwide. Provide high quality site management service for well-known pharmaceutical companies including MSD, PXL, Akesobio, Zelgen, Novartis, Hengrui, Bristol-Myers Squibb, Henlius, Eli Lilly, and Labcorp.
As of Jun 30, 2022, ClinPlus has more than 3,400 professionals serving over 740 clinical trial research institutions, out of the 1,100 ones it is able to cover. ClinPlus is able to fulfill the needs of our clients in most projects by being able to provide services in about 160 cities in most provinces across the country.
We cover the mainstream disease spectrum, such as tumor, endocrine, cardiovascular, respiratory, virus, etc.
We are involved in Phase I-III and post-marketing surveillance
Clients include world-renowned new drug R&D companies, CRO companies, and most domestic new drug companies and mainstream pharmaceutical companies.
ClinPlus was awarded the first PD-1 project in China: Bristol-Myers Squibb's research in Navulamumab for treating lung cancer;
ClinPlus was awarded the first CAR-T project: JW's Therapeutics's research in CD19 compound antigen receptor T cell injection for treating B-cell non-Hodgkin lymphoma;
The first monoclonal antibody drug in China for treating hyperlipidemia-Rebbegan by Amgen Biotech, awarded to ClinPlus, was successfully listed in the market;
The first direct oral anti-hepatitis C virus drug, Sofosbuvir tablets, awarded to ClinPlus, was approved to be sold in the market.
The world's first approved biologic Beliuximab for treating systemic lupus erythematosus, awarded to ClinPlus, was approved to be sold in the market.
The first domestic human papillomavirus vaccine in China-Xinkonin, awarded to ClinPlus, was approved to be sold in the market.
ClinPlus assisted sponsor to get NDA for the world's first and only approved ADC drug targeting Trop-2, the first domestic double antibody and the world's first PD-1/CTLA-4 double antibody and other innovative drugs.
To form a model by fully integrating previous performances in operation, including site selection, SSU, patient enrollment, risk management, quality control, database, investigators' fee, patient expenses. By establishing a relatively realistic and reliable model during the start of the project, we can help our clients find a more robust and practical implementation plan to improve efficiency and maximize the benefits of resource allocation.