Phase I a/b SAD/MAD study to evaluate safety and tolerability of LBT-3627 in both healthy volunteers and Parkinson's patients.
Evaluate the safety and tolerability of LBT-3627 in both a single and multiple ascending dose study. Phase Ia will explore safety and tolerability first in healthy volunteers then followed by Parkinson's patients after a single dose. Dose levels will escalate per cohort. Phase Ib will explore safety and tolerability in Parkinson's patients after multiple doses. Dose levels will escalate per cohort.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
64
Alfred Hospital
Melbourne, Victoria, Australia
RECRUITINGMonash Medical Center
Melbourne, Victoria, Australia
RECRUITINGNucleus Networks
Melbourne, Victoria, Australia
ACTIVE_NOT_RECRUITINGIncidence, nature, and severity of adverse events [Safety and Tolerability]
Time frame: Day of treatment to end of follow-up period (1, 2 or 4 weeks)
Maximum Plasma Concentration [Cmax]
The peak plasma concentration of a drug after administration.
Time frame: Day of treatment to end of follow-up period (1, 2 or 4 weeks)
Elimination half life [T1/2]
The time required for the concentration of the drug to reach half of its original value.
Time frame: Day of treatment to end of follow-up period (1, 2 or 4 weeks)
Time to reach Cmax [Tmax]
Time required to reach Cmax.
Time frame: Day of treatment to end of follow-up period (1, 2 or 4 weeks)
Volume of Distribution [Vd]
The apparent volume in which a drug is distributed (i.e., the parameter relating drug concentration in plasma to drug amount in the body).
Time frame: Day of treatment to end of follow-up period (1, 2 or 4 weeks)
Concentration [C]
Amount of drug in a given volume of plasma
Time frame: Day of treatment to end of follow-up period (1, 2 or 4 weeks)
Area under the curve [AUC]
The integral of the concentration-time curve (after a single dose or in steady state).
Time frame: Day of treatment to end of follow-up period (1, 2 or 4 weeks)
Clearance [CL]
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The volume of plasma cleared of the drug per unit time.
Time frame: Day of treatment to end of follow-up period (1, 2 or 4 weeks)
Bioavailability [f]
The systemically available fraction of a drug.
Time frame: Day of treatment to end of follow-up period (1, 2 or 4 weeks)