RE: FDA EUA approval takes days23 Jul 2020 21:31
Sparkle - The nebuliser used to administer the drug is the I-neb, I believe it is manufactured by Philips healthcare.
Our patents cover the formulation used to deliver IFN-b in a nebuliser format to the lungs and upper respiratory tract to combat influenza type viruses. So it is pretty encompassing and a solid parent which AZN where happy to cut a deal on previously.
The company has been very open about the end game here which is to transact with a major pharmaceutical. They have been working and are continuing to work towards eliminating the risks surrounding the asset. These preliminary results where a major milestone, they have worked on manufacturing and supply chain also.
Next risks to eliminate are approvals FDA, EUA, MRHA and inevitably a much larger phase 3 study.
The further along they get with this process the more valuable the asset becomes, Covid is a very timely pandemic for Synairgen.
By the end of the year hopefully there will be 1000’s of patient data for the drug.
The transaction with a big pharma/s will either come in the form of licensing deals or a takeover.
Licensing deals would probably bring maximum shareholder value, a takeover would bring less shareholder value but quicker and eliminates the guess work of when to call the top.