M1069 / EMD Serono, Domain Therap 
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  • ||||||||||  M1069 / EMD Serono, Domain Therap
    Enrollment open, Metastases:  MS201929_0032: First in Human Study of M1069 in Advanced Solid Tumors (clinicaltrials.gov) -  Apr 1, 2022   
    P1,  N=24, Recruiting, 
    Recruiting --> Active, not recruiting Not yet recruiting --> Recruiting
  • ||||||||||  M1069 / EMD Serono, Domain Therap
    M1069 as dual A2A/ A2B adenosine receptor antagonist counteracts immune-suppressive mechanisms of adenosine and reduces tumor growth in vivo (Section 37) -  Mar 9, 2022 - Abstract #AACR2022AACR_5472;    
    These findings were further corroborated with the results from in vivo studies in a murine CD73hi/adenosine-rich 4T1 syngeneic breast tumor model, in which M1069, but not an A2A-selective antagonist, reduced tumor growth as a monotherapy and enhanced anti-tumor activity with chemotherapeutic agents. In summary, M1069 is a potent, dual A2A/A2B adenosine receptor antagonist, which is expected to counteract immune-suppressive mechanisms in the presence of high concentrations of adenosine and enhance the anti-tumor activity of chemotherapies.