Licence28 Mar 2021 15:45
Extract from Jaylarcs post yesterday;
'
We all know Avactas AVA6000 prodoxorubicin is about to start clinical trials and if the data received by end of 2021 is positive this will allow a further pipeline of pro chemo drugs.
If AVA6000 results in humans shows even 25% of what it has shown in animal models it will be a massive improvement on the standard chemo drugs.
Avacta have 3 further prodrugs ready to go immediately on successful data.
TAM
Duxorubicin $1 billion
Velcade $1.2 billion (2018)
Paclitaxel $3 billion
Oxaliplatin $0.9 billion
Total $6.1 billion and thats a small part of a $50 billion chemo drug market that we could eventually target.
As these are generic and either off patent or about to come off patent, they are reasonably cheap (Duxorubican I think is $17 a pop),a pro drug version of these could easily be sold for double and still be a cheap treatment. Who in their right mind would want to save a $17 on a less efficent chemo drug? Nobody the whole market would be for the pro version.
Also the pro drugs will take the complete market share from the standard drug.
$6.1 billion x Double the cost = $12.2 billion
As well as this the amount of pro chemo drug safely taken can easily be doubled or tripled, lets say double.
$12.2 bllion x twice as much product sales = $24.4 billion
Again the pro drug can be taken by lots more patients that otherwise could not due to health issues such as a weak heart etc. Say a 25% increase in patient numbers.
$24.4 biliion +25% amount of patients= $30.5 bilion
There are a lot of unscrupulous charcacters on this BB that would try to make you believe that revenues from PreCision will be many years away.
Well we heard from the horses mouth in todays interview that we will have data on prodoxorubican by end 2021 and if successful that will enable our other 3 prochemo drugs to move immediately into trials.
AS also said that due to duxirubican being a well known and understood drug means AVA6000 will be ready to go after phase 2 trials, phase 3 is not needed, phase 2 will be "pivotal" and give "market approval".
Ignoring the Covid opportunities, all the other diagnostics, the many collaborations, joint venture, TMAC and god knows whatever else pops up along the way, you can see why AS mentions us in same breath as Abbott, Roche etc.'
Imagine the revenue from licencing our 'pro' version of these drugs to their originators?
They have an established market which can be extended as stated above and they get a new 20 year patent to go with it....... and our cash register goes ch..ching.