Fortunately, yes.
In short:
- Tom gave rundown of company/trial history.
- Recent third-party analysis by Clarivate determined impact stemming from new weight loss drugs (Ozempic, Wegovy etc) to future revenue/potential market for Invex was very high.
- Board decided to finalise Phase III trial to protect capital and minimise expenses.
- Focus now appears to be on TBI and other potential similar use cases (meningitis, hydrocephalus etc).
- Other “strategic options” all on the table (including handing cash back to shareholders, should that be deemed a suitable path by the Board).
- Rep from Candour Advisory was the only caller to ask multiple questions – primarily on upcoming expenditure, strategic options moving forward, cash burn and TBI market (addressing the fact that the TBI market is quite competitive in the bio space).
- Final cash position to be ascertained once trial is completely finalised. Invex to inform market once they have all the necessary details.
Near term catalysts
- Invex also expects to secure Orphan Drug Designation for Exenatide in TBI from the US FDA, also in CY2023.
- The company continues to develop plans for a proof-of-concept Phase II clinical trial in moderate to severe TBI with Exenatide.
- Costs regarding dosing regimens and route of administration for such a trial were said to be minimal (low cash burn).
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