RE: Which Product will License First ?22 Sep 2021 19:26
I have added the question to the Q & A portal of Meet the Company. I'm sure they will cover these areas off comprehensively and update us anyhow but have uploaded the following just the same:-
Can you update us please regarding which Project Is Likely to License First? On your website you previous stated: -
“VAL201 has completed a Phase 1/2 clinical trial, so is required to complete Phase 2 and 3 before market authorisation can be considered – the timeline for this will be dependent on the design of those trials”
“VAL301 is at preclinical stage, so requires all three clinical phases of development”
“VAL401 has a shorter route to market due to the nature of it as a reformulated generic drug, and requires at least one further clinical trial (depending on size and results) before market authorisation could be considered”
Therefore, of these three pipeline products, VAL401 can be considered furthest along the development pipeline. However, the timing of market authorisation is difficult to predict, especially as it is controlled by a third party.
Since then, we understand things have advanced somewhat, the Japanese partner working on Val301 has been involved for 17mths now, can you update on their progress?
Are we now closer to any form of market authorisation for Val 401, typically how long on average do they tend to take?
Thanks in advance