Clinical Study of JS007 in Patients With Advanced Solid Tumors

  • STATUS
    Recruiting
  • days left to enroll
    41
  • participants needed
    42
  • sponsor
    Shanghai Junshi Bioscience Co., Ltd.
Updated on 29 November 2021

Summary

This is an open label, phase Ia clinical study to evaluate the safety, tolerability, pharmacokinetic (PK) profile, pharmacodynamic (PD) profile, immunogenicity and preliminary efficacy of JS007 in the patients with advanced solid tumors who have progressed after standard of care, or lack of effective standard therapeutic regimen. This study is divided into two periods: dose escalation period, dose expansion period.

Details
Condition Patients With Advanced Solid Tumors
Treatment JS007
Clinical Study IdentifierNCT05049265
SponsorShanghai Junshi Bioscience Co., Ltd.
Last Modified on29 November 2021

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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