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Clinical Trial Summary

To assess the longer term safety, tolerability, and LDL C lowering efficacy after 52 weeks of additional treatment with LIB003 with subcutaneous (SC) dosing every 4 weeks (Q4W)


Clinical Trial Description

To assess the longer term safety, tolerability, immunogenicity, PK, PD and LDL C lowering efficacy after 52 weeks of additional treatment with LIB003 with subcutaneous (SC) dosing every 4 weeks (Q4W) in patients on stable maximally tolerated statins with or without ezetimibe who completed the phase 2 dose ranging trial LIB003-002 ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03847974
Study type Interventional
Source LIB Therapeutics LLC
Contact
Status Completed
Phase Phase 2
Start date February 14, 2019
Completion date August 31, 2020

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