RE: Inside pharma mole3 Feb 2023 09:35
The debate currently being held on this forum is mainly due to RM’s ‘multiple arrows’ comment, as the term is so vague it is open to interpretation and has left investors without a clearly defined pathway to success. As we know the market hates uncertainty, which has been reflected in the declining share price, leaving LTHs the target for ridicule from a minority of flawed characters on this board.
Given the rarity of public comment out of Southampton HQ, you would imagine when one of them eventually speaks it would be with absolute clarity, but not in this case, Richard loves to keep us hanging on in there with obtuse phrases.
One of my less charitable investment buddies, who uses more ‘industrial’ language interpreted the comment as, ‘throw so much $hit at the wall, hoping some of it will stick.’ Hard to argue with that viewpoint at the time.
It would have been beneficial if Marsden had clearly specified whether they were aiming for several trials running simultaneously, or one single entity involving many more patients treating a ‘broad spectrum’ at the same time, with varying results running side by side.
Gunto reckons there is now clarity regarding this, but nothing is certain as IMO the American’s will ultimately make the decision.
A ‘broad spectrum’ treatment is obviously the Nirvana that all pharma companies aspire to, but in reality there is always the small matter of FDA clearance to overcome. Anyone who has been invested with other pharma companies will know this is a long, tedious process that generally takes 1-2 years to complete.
I am not cross ramping here, but I will mention Angle PLC, as they have recently completed the tortuous process of FDA approval.
They have a new piece of tech that offers early detection of cancer without the need for biopsy, but when they initially opened up discussions with the FDA to seek advice on the pathway forward they were advised to study and obtain results for breast cancer only, followed by separate studies and results for ovarian, prostate and so on.
They were specifically advised that approval to sell their tech to cover all cancer types was out of the question from day one.
I obviously highlight this as there is a clear parallel to be drawn with SNG’s ‘broad spectrum’ approach. Given this scenario, I'm hoping, no at this stage, praying that we secure a place on the STRIVE covid P3 bandwagon. Decent P3 results here - The rest should follow.
Several posters have voiced concerns that we would lose control over the protocol, endpoints etc, but at this point we have little choice but to put our trust in the Americans, as we lost control over our own destiny after Sprinter and whether we like it or not, the USA hold the cards that matter. They have the cash, the BPs and the FDA.
There is enough evidence to suggest that SNG will be included on STRIVE P3, as they have clearly stated the treatment ‘merits further investigation’, whether Strive P3 materialises only time wil