Table 2.

Published third-party EST trials

StudyYearTargetNSerious adverse eventsClinical results
94  2007 EBV 33 None 52% CR/PR 
81,95  2010, 2012 EBV None 4/5 CR 
97  2013 CMV, EBV, Adv 50 8 cases GVHD
(2 de novo) 
74% CR/PR 
96  2017 CMV, EBV, Adv, BK, HHV6 38 2 cases of de novo GVHD (grade 1) 92% CR/PR 
92  2018 CMV, EBV, Adv 30 2 cases of de novo GVHD 93% CR/PR 
90  2020 EBV 46 None 68% CR/PR (BMT)
54% CR/PR (SOT) 
StudyYearTargetNSerious adverse eventsClinical results
94  2007 EBV 33 None 52% CR/PR 
81,95  2010, 2012 EBV None 4/5 CR 
97  2013 CMV, EBV, Adv 50 8 cases GVHD
(2 de novo) 
74% CR/PR 
96  2017 CMV, EBV, Adv, BK, HHV6 38 2 cases of de novo GVHD (grade 1) 92% CR/PR 
92  2018 CMV, EBV, Adv 30 2 cases of de novo GVHD 93% CR/PR 
90  2020 EBV 46 None 68% CR/PR (BMT)
54% CR/PR (SOT) 

Shown are published results of prior clinical trials demonstrating safety of third-party ESTs.

Adv, adenovirus; BMT, bone marrow transplantation; CMV, cytomegalovirus; PR, partial response.

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