Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Study of MBX 2109 in Healthy Adult Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

76

Participants

Timeline

Start Date

November 10, 2021

Primary Completion Date

June 20, 2023

Study Completion Date

June 20, 2023

Conditions
Healthy
Interventions
DRUG

MBX 2109 (Part A)

Single ascending SC dose of MBX 2109: 50 µg, 150 µg, 300 µg, 460 µg, 600 µg

DRUG

MBX 2109 (Part B)

Repeated ascending SC doses of MBX 2109: 200 µg, 300 µg, 460 µg, 600 µg, 900 µg

DRUG

Placebo

Single SC dose or repeated SC doses of placebo.

Trial Locations (2)

53704

Labcorp Drug Development: Clinical Research Unit, Madison

75247

Labcorp Drug Development: Clinical Research Unit, Dallas

Sponsors

Lead Sponsor

All Listed Sponsors
lead

MBX Biosciences

INDUSTRY

NCT05158335 - Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Study of MBX 2109 in Healthy Adult Subjects | Biotech Hunter | Biotech Hunter