This is a 2-part, first-in-human, open-label study to determine the safety, tolerability and preliminary efficacy of KIVU-305, a CEACAM5-directed antibody-drug conjugate, in participants with locally advanced or metastatic solid tumors.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
76
KIVU-305 will be administered IV .
Kivu Trial Site
Sydney, New South Wales, Australia
RECRUITINGKivu Trial Site
Wollongong, New South Wales, Australia
RECRUITINGKivu Trial Site
Brisbane, Queensland, Australia
RECRUITINGTo determine Maximum tolerated dose (MTD)
Number of participants with treatment emergent adverse events as assessed by CTCAE Version 6.0.
Time frame: up to 18 months
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