TD-1607, administered intravenously as multiple ascending doses, will be investigated in healthy subjects to assess its tolerability, safety, and pharmacokinetics.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
48
PPD, Phase 1 Clinic
Austin, Texas, United States
Number of adverse events
Adverse events
Time frame: 17 days
Cmax
Pharmacokinetics
Time frame: 17 Days
Tmax
Pharmacokinetics
Time frame: 17 Days
AUC0-t
Pharmacokinetics
Time frame: 17 Days
AUC0-24
Pharmacokinetics
Time frame: 17 Days
AUCinf
Pharmacokinetics
Time frame: 17 Days
CL
Pharmacokinetics
Time frame: 17 Days
Vdss
Pharmacokinetics
Time frame: 17 Days
t1/2
Pharmacokinetics
Time frame: 17 Days
Amount excreted in urine (Ae
Pharmacokinetics
Time frame: 17 Days
Fraction eliminated in urine (fe)
Pharmacokinetics
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Time frame: 17 Days
CLr
Pharmacokinetics
Time frame: 17 Days
Ctrough
Pharmacokinetics
Time frame: 17 Days