A Phase 1 Clinical Study Of BW-20805-2-1001 in Healthy Participants
A Phase 1, Open-Label, Single Dose Bridging Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Subcutaneously Administered BW-20805-2 in Healthy Participants
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
24
Cohort 1 will receive SC administrations of BW-20805 on Day1.
Group 2 will receive SC administrations of BW-20805 on Day1
Group 3 will receive SC administrations of BW-20805-2 on Day1.
Nucleus Network Pty Ltd.
Melbourne, Victoria, Australia
Primary Endpoints
Incidence and severity of adverse events (AEs) and serious adverse events (SAEs)
Time frame: week 48
Secondary Endpoints
Maximum observed plasma concentration (Cmax), - Time to maximum plasma concentration (Tmax),
Time frame: week 48
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