This Phase 1 study will evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of ADX-850 in participants with hypertension.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
28
CMAX Clinical Research
Adelaide, South Australia, Australia
Linear Clinical Research
Nedlands, Western Australia, Australia
Clinitrials Pty Ltd
Perth, Australia
Safety of ADX-850 in Participants with Hypertension
Incidence, relationship and severity of adverse events and serious adverse events
Time frame: 365 days
Pharmacokinetics (PK) of ADX-850 - Maximum Concentration
Cmax
Time frame: 8 days
Pharmacokinetics (PK) of ADX-850 - Time to Maximum Concentration
Tmax
Time frame: 8 days
Pharmacokinetics (PK) of ADX-850 - Exposure
Area under the Curve (AUC)
Time frame: 8 days
Pharmacodynamics (PD) of ADX-850 - Blood Pressure
Change from baseline in blood pressure
Time frame: 365 days
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