The purposes of this clinical study are 1. To see how the new drug (HMB-003) under study is tolerated in healthy volunteers, and if there are any important side effects. 2. To measure the amount of HMB-003 in the body after injection.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
40
Worldwide Clinical Trials
San Antonio, Texas, United States
RECRUITINGNumber of participants with treatment emergent adverse events (TEAEs)
Time frame: From Day 1 up to 42 days after a single dose of study drug on Day 1
Plasma concentration of HMB-003
Time frame: From 0 hours (pre-dose) to 42 days after a single dose on Day 1
Urine concentration of HMB-003
Time frame: From 0 hours (pre-dose) to 42 days after a single dose on Day 1
Pharmacodynamic parameter: Clot lysis
Time frame: From 0 hours (pre-dose) to 42 days after a single dose on Day 1
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