SL-172154 / Shattuck 
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  • ||||||||||  SL-172154 / Shattuck
    Enrollment closed, Trial completion date, Trial primary completion date, Combination therapy:  SL03-OHD-104: Phase 1 Study of Shattuck Labs (SL)-172154 in Subjects with MDS or AML (clinicaltrials.gov) -  Oct 2, 2024   
    P1,  N=160, Active, not recruiting, 
    Trial completion date: Apr 2025 --> Nov 2024 Recruiting --> Active, not recruiting | Trial completion date: Dec 2025 --> Nov 2024 | Trial primary completion date: Apr 2025 --> Nov 2024
  • ||||||||||  SL-172154 / Shattuck
    Enrollment change, Trial completion date, Trial primary completion date, Combination therapy:  SL03-OHD-104: Phase 1 Study of Shattuck Labs (SL)-172154 in Subjects with MDS or AML (clinicaltrials.gov) -  Mar 26, 2024   
    P1,  N=160, Recruiting, 
    Enrolling by invitation --> Active, not recruiting N=107 --> 160 | Trial completion date: Oct 2024 --> Dec 2025 | Trial primary completion date: Feb 2024 --> Apr 2025
  • ||||||||||  SL-172154 / Shattuck
    Trial completion, Trial completion date:  Phase 1 Study of SL-172154 (SIRP?-Fc-CD40L) in Subjects With Ovarian Cancer (clinicaltrials.gov) -  May 18, 2023   
    P1,  N=34, Completed, 
    A response to SL-172154 monotherapy, dose-dependent increases in serum cytokines and accumulation of mature myeloid cells in BM suggest a potential role for CD40 stimulation. Active, not recruiting --> Completed | Trial completion date: Jul 2023 --> Feb 2023
  • ||||||||||  SL-172154 / Shattuck
    Enrollment closed, Trial completion date, Trial primary completion date:  Phase 1 Study of SL-172154 (SIRP?-Fc-CD40L) in Subjects With Ovarian Cancer (clinicaltrials.gov) -  Nov 3, 2022   
    P1,  N=34, Active, not recruiting, 
    Maximal CD47 and CD40 target engagement and CD40-dependent PD effects were observed with ?3mg/kg SL-172154. Recruiting --> Active, not recruiting | Trial completion date: Jul 2022 --> Jul 2023 | Trial primary completion date: Jul 2022 --> Mar 2023
  • ||||||||||  SL-172154 / Shattuck
    [VIRTUAL] CD40 Enhances Type I Interferon Responses Downstream of CD47 Blockade to Bridge Innate and Adaptive Immunity () -  Aug 31, 2020 - Abstract #PEGS2020PEGS_295;    
    CD47/SIRPa blockade enhances macrophage-mediated phagocytosis of tumor cells that are dying, or have been tagged with an ADCP-competent antibody, however this event does not enhance anti-tumor immunity in the absence of antigen presentation to CD8+ T cells. SIRPa-Fc-CD40L (SL-172154) links these two mechanisms via a Type I interferon response, and has shown profound activity in both mouse and non-human primate studies.
  • ||||||||||  SL-172154 / Shattuck
    Enrollment open:  Phase 1 Study of SL-172154 (SIRP?-Fc-CD40L) in Subjects With Ovarian Cancer (clinicaltrials.gov) -  Jul 13, 2020   
    P1,  N=33, Recruiting, 
    SIRPa-Fc-CD40L (SL-172154) links these two mechanisms via a Type I interferon response, and has shown profound activity in both mouse and non-human primate studies. Not yet recruiting --> Recruiting