Licence or Buyout10 Dec 2025 14:27
Much recent debate about deal being to licence p140 or a full blown IMM acquisition. One part that has been overlooked in discussion and which, imo, has an important role to play is that of Avion. They are still here but in capacity unknown.
I’ve been back through RNSs relating to Avion starting with the trial failure RNS of 17/04/2018 (time flies when you’re enjoying yourself!!).
First, consider the difference between Lupuzor and p140. Lupuzor was nothing more than a branding of the peptide p140 as, at the time, it was being targetted primarily at SLE (lupus). I believe this was a commercial decision as, surely, CNRS, in their research, would have observed some efficacious effect with other autoimmune indications?
Lupuzor and p140 appeared jointly and separately in many RNs subsequent to 17/04/2018 but was then dropped following the RNS of 02/04/2024 when the new IP strategy was initiated. In short, Lupuzor was/is p140 without the enhancements and diagnostic capability announced in the RNSs of 09/01/2025 and 13/03/2025.
The RNS of 28/11/2019 announced the Lupuzor licence agreement with Avion from which the following, “ImmuPharma will also receive $5 million for each additional approval, other than lupus, as Avion also has the rights, for the US, {to explore further opportunities within Lupuzor™'s peptide platform for other auto-immune indications outside of lupus{.” Note the final words which I’ve highlighted. The peptide platform referenced is p140.
Also in this RNS, a new lupus trial was targetted to commence in 2020. After much interaction with the FDA, this was then updated in 09/02/2021 advising an international Ph3 trial would commence in H2 2021. Further to more interaction with the FDA on drug and trial details, the RNS of 19/06/2023 then confirmed a Ph2/3 adaptive trial would start in H2 2023. The delays were not down to subterfuge on the part of IMM, as some would suggest, but purely the time needed to respond to and reshape trial parameters to meet FDA demands. Since then.......silence! Why?
The RNSs announcing the wider application of p140 in autoimmune diseases and of the diagnostic capability came little more than 18 months after the last RNS relating to the Avion Ph2/3 trial. The further research into p140 following 2018’s failure would have been well advanced by then and I am certain that Avion would have been made aware of these developments. What would you have done with that knowledge??
One of the major reasons for the 2018 failure was down to participant profiling and the inclusion of individuals who were never going to respond positively to p140. Using the new diagnostic capability to profile participants, a trial success is all but guaranteed. Why would Avion start a trial when they may well have known about the reduced risk from using the p140 diagnostics to profile participants? Is this the reason for the silence as they renegotiate their agreement with IMM?
My opinion and I'm not a