RE: Give us a clue…6 May 2022 17:18
Don't think the 1:18 matters at this point, Timster.
According to the Clinical Trial criteria "This open-label, First-into-Human (FIH) study will evaluate the safety, tolerability, pharmacokinetics (PK) and early efficacy of AVA6000, a FAP-activated pro-drug of doxorubicin, in patients with locally advanced and/or metastatic solid tumours. In Phase Ia, using a 3+3 design, escalating doses of AVA6000 will be administered to patients with a range of solid tumour types to determine the maximum tolerated dose (MTD) and/or recommended Phase II dose (RP2D). In Phase 1b, the selected RP2D dose will be assessed in one to three tumour types."
I have taken that to mean that safety and tolerability are key initially and The Safety Committee have agreed that they have been, so we move forward. It works (so far then) it would seem.
Onwards Avacta.