RE: LSE16 May 2023 09:13
Dougie/The.Italian
I suspect the China syndrome is progressing as expected and I am sitting in anticipation of an early call to say they have submitted the NDA, however. The FDA Phase 3 cannot progress without an injection of cash which is why they have gone for the SPA in the hopes it may convince a US licensee to commit, however. Given all the jam tomorrow put out by the company before regarding the FDA approval process, I'm not going to hold my breath and now don't expect approval till more likely the end of 2026/beginning of 2027 (best forgotten about at the moment, what a disaster it has been).
The European income will be next to nothing given the manufacturer is only issuing 30k cans every 3 months which will be sold at around 40Euros/can (180k GBP to ERP based on 15%), so China is the place for me....lol
Interestingly, JG thinks the FDA phase III study is completed, according to the April 17th Operational update.
Jamie Gibson, CEO of the Group, said “We are delighted with these highly significant and positive results from the Phase 3 clinical study in China, which reinforces the results from the European and US Phase 3 clinical studies".
OMG.....:-O they've been lying to us all along !!!