Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
This is a randomized, double-blind, placebo-controlled, dose-increasing Phase I clinical trial to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of a single intravenous infusion of LPM3480392 injection in healthy subject
A total of 80 healthy subjects will be allocated to 1 of 8 cohorts (cohort 1~8) in the study, each cohort including 10 subjects (8 subjects will receive investigational new drug (IND) product and 2 receive placebo). Each subject in fasted state will be randomly assigned to receive a single dose of LPM3480392 or placebo intravenously.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| LPM3480392 X1mg | Experimental | 8 subjects will receive LPM3480392 X1mg and 2 receive placebo |
|
| LPM3480392 X2mg | Experimental | 8 subjects will receive LPM3480392 X2 mg and 2 receive placebo |
|
| LPM3480392 X3mg | Experimental | 8 subjects will receive LPM3480392 X3mg and 2 receive placebo |
|
| LPM3480392 X4mg | Experimental | 8 subjects will receive LPM3480392 X4mg and 2 receive placebo |
|
| LPM3480392 X5mg | Experimental | 8 subjects will receive LPM3480392 X5mg and 2 receive placebo |
|
| LPM3480392 X6mg | Experimental |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| LPM3480392 | Drug | Intravenous infusion of 30min duration |
|
| Measure | Description | Time Frame |
|---|---|---|
| Incidents of AE (including SAE) | (including abnormal value of Vital signs,physical examination,laboratory tests,12-lead ECG) | from baseline to day8 |
| DEQ | Drug effect questionnaire, | from baseline to day2 |
| OWS | Opiate Withdrawal Scale | from baseline to day3 |
| Measure | Description | Time Frame |
|---|---|---|
| AUC0-t | Pharmacokinetic index | baseline and 48 hours after administration |
| AUC0-∞ | Pharmacokinetic index | baseline and 48 hours after administration |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The second affiliated hosipital zhejiang university school of medicine | Hangzhou | Zhejiang | 310000 | China |
Not provided
Not provided
Not provided
Not provided
Not provided
8 subjects will receive LPM3480392 X6mg and 2 receive placebo
|
| LPM3480392 X7mg | Experimental | 8 subjects will receive LPM3480392 X7mg and 2 receive placebo |
|
| LPM3480392 X8mg | Experimental | 8 subjects will receive LPM3480392 X8mg and 2 receive placebo |
|
| Placebo | Drug | Intravenous infusion of 30min duration |
|
| Cmax | Pharmacokinetic index | baseline and 48 hours after administration |
| Tmax | Pharmacokinetic index | baseline and 48 hours after administration |
| T1/2 | Pharmacokinetic index | baseline and 48 hours after administration |
| CL | Pharmacokinetic index | baseline and 48 hours after administration |
| Vd | Pharmacokinetic index | baseline and 48 hours after administration |
| MRT | Pharmacokinetic index | baseline and 48 hours after administration |
| λz | Pharmacokinetic index | baseline and 48 hours after administration |
| PD profile : Cold Pain Test | Pharmacodynamic index | baseline and 8 hours after administration |
| PD profile : Pupillometry | Pharmacodynamic index | baseline and 8 hours after administration |