About Cliniboosta

Cliniboosta is an innovative platform dedicated to providing end-to-end services for Investigator-Initiated Trials (IIT) in China. We deeply integrate clinical research resources, facilitate an accelerated parallel connection mechanism for clinical trials between China, the US, the UK, and Europe, and foster an efficient domestic IIT service ecosystem. We offer comprehensive support to pharmaceutical R&D companies, spanning from project initiation to data management. By 2025, we have successfully assisted in the implementation of multiple IIT projects across various therapeutic areas, including oncology, rare diseases, autoimmunity, metabolic & chronic diseases, and neurodegenerative diseases. Acting as a core partner for global pharmaceutical companies advancing clinical innovation in China, Cliniboosta is committed to accelerating the translation of scientific research into clinical applications, ultimately benefiting patients both in China and abroad.

Our Full Process IIT Service
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Caseproject Milestone Timeline
M 0

• Initial presentations to PI

• Hold meetings with PI for 

  revision discussion of the 

  trial protocol

• Began to write the 

  Investigator’s brochure


M 1

• Prepared documents of 

  project approval

• Negotiation with sample 

   testing laboratory

• Negotiation with SMO

• Negotiation with company 

   on data management and 

   statistical analysis


M 2

• Finalized protocol details 

   with research center

• Revised and finalized

   study protocol


M 3

• Prepared the IIT protocol

• Signed agreements with 

   each service provider

• Submitted project approval

   information to the center

• Project successfully 

   registered in research

   center


M 4

• The research center

   obtained ethical approval

• Signed the clinical

   trial protocol


M 6

• Held IIT Launch meeting at

   the research center 

• The first informed consent

   form was signed the next

   day 

• The first patient received

   treatment within 2 weeks

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Email
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