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Clinical Trials associated with bacTRL-IL-12A Multi-centre, Open-label, Phase I Trial of bacTRL-IL-12 in Adult Subjects With Advanced, Treatment-refractory Solid Tumours
This study is as an open-label study to be conducted at multiple study centres across New Zealand and Australia designed to characterise the safety, tolerability and preliminary assessment of the anti-tumour efficacy of bacTRL-IL-12 after intravenous (IV) infusion.
The study will consist of a screening period (Day -14 to Day -2), treatment and observation (Day 1 to Day 22), safety follow-up period (Day 28 to Day 31), and efficacy follow-up period (until progression, death, revocation of consent, or lost to follow-up).
100 Clinical Results associated with bacTRL-IL-12
100 Translational Medicine associated with bacTRL-IL-12
100 Patents (Medical) associated with bacTRL-IL-12
100 Deals associated with bacTRL-IL-12