RE: Investment Management4 Feb 2026 06:15
Correct, and that execution risk largely comes down to trial design and patient selection. The ability of Avacta now to establish optimal dosage, starting with ava6000 basically ensures that the regime they take into P2/3 will have already shown capability for efficacy and extensions of survival endpoints. Risk of failure in further studies greatly reduced. Path to accelerated approval is set out. So all that needed now is the funding partnership for this drug to be revealed.