drugset / Trial / NCT03760913

OLP-1002 is Being Studied in the Treatment of Pain.

NCT03760913 ↗

Phase 0 Completed 116 enrolled OliPass Corporation
RandomizedParallel-groupTriple-blindTreatment

Summary

The primary objective of the study is to assess the safety and tolerability of single and multiple subcutaneous doses of OLP-1002 in healthy subjects.

Timeline

Start
2018-11-21
Primary completion
2020-10-16
Completion
2020-10-16

Drugs

EvaluationDrugModalityDoseRoute
Subject OLP-1002 Unknown 30 ng Subcutaneous
Subject OLP-1002 Unknown 120 ng Subcutaneous
Subject OLP-1002 Unknown 400 ng Subcutaneous
Subject OLP-1002 Unknown 1.2 ug Subcutaneous
Subject OLP-1002 Unknown 2 ug Subcutaneous
Subject OLP-1002 Unknown 3 ug Subcutaneous
Subject OLP-1002 Unknown 5 ug Subcutaneous
Subject OLP-1002 Unknown 6 ug Subcutaneous
Subject OLP-1002 Unknown 10 ug Subcutaneous
Subject OLP-1002 Unknown 12 ug Subcutaneous
Subject OLP-1002 Unknown 20 ug Subcutaneous
Subject OLP-1002 Unknown 40 ug Subcutaneous
Subject OLP-1002 Unknown 80 ug Subcutaneous
Subject OLP-1002 Unknown 160 ug Subcutaneous

Indications

No indication recorded.