The purpose of this study is to assess the safety, tolerability and blood levels of LBR-101 when administered intravenously or subcutaneously to healthy volunteers.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
QUADRUPLE
Enrollment
36
LBR-101 Administered Intravenously
LBR-101 Administered Subcutaneously
PPD Development
Austin, Texas, United States
Relative bioavailability of IV versus SC Administration of LBR-101
Time frame: 30 Days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.