I have spent years working with 1,4-andro, so I am in a good position to comment on this. The base structure of 1,4-androstadienes allows these molecule to resist 17-ketosteroid reduction to a fair degree, much better than other natural steroid hormones like nandroloe and testosterone. The acetate may protect a little more, but it will not be the primary protective group. Dehydrogenation of C1-2 is the cause for shifting redox potential.
In the end, it should have "fair" oral bioavailability. I would suspect you'd take your normal weekly dose on a daily basis, at a minimum, for a similar effect. It will wort of be like Primobolan orals, or trenbolone acetate orals.
I don't expect it will be very cost effective, but for that small group that hates needles it might be a less toxic alternative. It would work better as a long-chain oil-solubilized ester, but cost for manufacture and handling/storage issues are also increased.