perenostobart (SRF617) / Coherus Biosci 
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  • ||||||||||  perenostobart (SRF617) / Coherus Biosci
    Trial completion, Enrollment change, Metastases:  KEYNOTE-A62: Study of SRF617 in Patients With Advanced Solid Tumors (clinicaltrials.gov) -  Aug 28, 2023   
    P1,  N=85, Completed, 
    Completed --> Terminated; The study was terminated for strategic reasons, not due to any safety concerns. Active, not recruiting --> Completed | N=177 --> 85
  • ||||||||||  perenostobart (SRF617) / Coherus Biosci
    Enrollment closed, Trial completion date, Trial primary completion date, Metastases:  KEYNOTE-A62: Study of SRF617 in Patients With Advanced Solid Tumors (clinicaltrials.gov) -  Nov 30, 2022   
    P1,  N=177, Active, not recruiting, 
    Recruiting --> Active, not recruiting | Trial completion date: Nov 2023 --> Jul 2023 | Trial primary completion date: Nov 2023 --> May 2023 Recruiting --> Active, not recruiting | Trial completion date: Nov 2022 --> Oct 2023 | Trial primary completion date: Oct 2022 --> Aug 2023
  • ||||||||||  SRF617 / Surface Oncology
    The fully human antibody SRF617 is a potent inhibitor of ecto-enzyme CD39 in vivo (Poster Hall) -  Oct 1, 2021 - Abstract #SITC2021SITC_330;    
    P1
    These studies demonstrate the therapeutic potential of targeting CD39 for the treatment of cancer. SRF617 is currently being evaluated in a Phase 1 clinical trial in patients with advanced solid tumors (NCT04336098) and in combination with chemotherapy in patients with pancreatic cancer.
  • ||||||||||  perenostobart (SRF617) / Coherus Biosci
    Enrollment change, Metastases:  KEYNOTE-A62: Study of SRF617 in Patients With Advanced Solid Tumors (clinicaltrials.gov) -  Dec 19, 2020   
    P1,  N=100, Recruiting, 
    SRF617 is currently being evaluated in a Phase 1 clinical trial in patients with advanced solid tumors (NCT04336098) and in combination with chemotherapy in patients with pancreatic cancer. N=56 --> 100