Read Between The Lines2 May 2020 01:12
Synairgen is now close to completing a Phase II study in COPD patients with confirmed respiratory viral infections and pre-existing significant impairment of lung function. With 109 out of a target 120 participants already dosed, this trial has been paused to minimise the chance of vulnerable patients being exposed to further infection risk and to minimise distraction for respiratory staff in the UK hospitals and GP sites conducting the trial, who will be at the forefront in dealing with patients suffering from COVID-19. The Company is currently exploring ways to adapt the trial to enable patients in the pre-treatment pool to be dosed if they become infected with SARS-CoV-2.
Early data from this double-blind, placebo-controlled trial have demonstrated that the antiviral responses in the lung (assessed using sputum biomarkers) are similar to those observed in the asthma trial, where we saw clinical benefit in lung function.
Use of proceeds
COVID-19 clinical trial activity GBP7m
Manufacture of SNG001 drug product and other supply GBP4m
chain considerations
Strengthened balance sheet for potential partnering GBP3m
discussions with regards to the COVID-19, future
pandemic preparedness, and the COPD opportunity,
working capital and fees
3. Current Trading and Future Prospects
Synairgen has recruited 109 of the 120 patients required for its IFN-beta trial in COPD, with data expected in Summer 2020. The opportunity now afforded to the Company with regards to COVID-19 is significant and the trial of SNG001 is expected to commence imminently. As at 31 December 2019, the Company had cash of approximately GBP2.45m (unaudited).
Looking to close out the Asthma Placebo trial by adapting the conditions for remaining 11 patients. Results Summer 2020 regardless of Covid activity.
This trial is also double blinded and placebo method. Yet note the paragraph reading Early Data, yet to be unblinded but they used Sputum Biomarkers to assess activity in the lung. Could this be the same way they have assessed Early Data from the current trial and hence pushed on to the extension, I think it could be, that’s why they are positive it works.
Look at the next bit use of proceeds, 4mill already assigned to manufacture the drug, I wonder how much of the 7 mill for the current trial is drug cost and how much is everything else? How much would 4 mill get? Then 3mill on top of current cash balance of 2.45 mill for future partnering discussions? Rumours of RM having meetings with Evercore I wonder what they do?? Or why he would need that meeting? I think there is so much to come here and believe a lot is going on in the background. They know they can’t go it alone so who are they going to sign up with? Deals for Covid and COPD IMO. The results from the previous COPD studies look perfect for Covid as the best results were shown with the people who would suffer most hence why they are being precise with recruitment.This has a high chance of being successfu