First-in-human Study to Assess Safety and Tolerability of a Single Subcutaneous Dose of SAR441255 in Lean to Overweight Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

April 25, 2019

Primary Completion Date

September 26, 2019

Study Completion Date

September 26, 2019

Conditions
OverweightHealthy Subjects
Interventions
DRUG

SAR441255

"Pharmaceutical form:solution for injection~Route of administration: subcutaneous"

DRUG

placebo

"Pharmaceutical form:solution for injection~Route of administration: subcutaneous"

Trial Locations (1)

37920

Investigational site number 8400001, Knoxville

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Sanofi

INDUSTRY