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Study to Assess the Safety and Tolerability of Single Doses of REGN1500

Hypertriglyceridemia Clinical Trial

Clinical Trial Summary

Phase 1, first-in-human, randomized, ascending single-dose, placebo-controlled, double-blind study of the safety, tolerability, and bioeffect of REGN1500

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01749878
Study type Interventional
Source Regeneron Pharmaceuticals
Contact Clinical Trials Administrator
Email clinicaltrials@regeneron.com
Status Recruiting
Phase Phase 1
Start date December 2012
Completion date May 2016
View Details
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