Agree. Looking forward to final tox/safety tests of RC220 being completed, ethics/governance will be the final hurdle - not sure of the average time for these approvals? I'm sure Dr T has everything lined up as much as possible to limit further wait time to be in the clinic.
I'm expecting no recruiting issues given the trial is 'all comers' and the benefit to the patient we all expect should see patients interested.
Next 12 months will be exciting.
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