Subcutaneous/orthotopic human CDX and PDX tumour xenografts in mice (lung, breast, prostate, ovary, pancreas, sarcoma and others)
“exhibited antitumor activity (decrease in the tumour volume or an increase in the survival time) against different experimental models of either subcutaneously or orthotopically xenografted human cell-derived (CDX) and patient-derived (PDX) tumours such as lung, breast, prostate, bladder, kidney, ovary, pancreas and sarcoma.”
Not reported in the public reviews. Reviewers summarise selectively, so this usually means it wasn't discussed publicly, not that it wasn't studied.
Reviewer's view of the efficacy data
EMA: tumour-microenvironment (transcriptional) effects shown only in vitro at low concentrations, with no in vivo confirmation
“The contribution of sub-lethal transcriptional mechanisms at antitumour doses in vivo remains unclear, as these effects have been demonstrated only in vitro at low concentrations (i.e. there is no in vivo confirmation of these effects).”