This is a Study to Evaluate the Safety, Tolerability, PK and PD of IV Administered ABL301 in Healthy Adult Participants

PHASE1CompletedINTERVENTIONAL
Enrollment

91

Participants

Timeline

Start Date

December 31, 2022

Primary Completion Date

April 30, 2025

Study Completion Date

April 30, 2025

Conditions
Healthy
Interventions
DRUG

ABL301

SAD: Participants will receive a single dose of ABL301 IV infusion, MAD: Participants will receive multiple doses of ABL301 IV infusion

DRUG

Placebo

SAD: single Placebo IV infusion, MAD: multiple Placebo IV infusion

Trial Locations (1)

78744

PPD Development, LP, Austin

Sponsors

Lead Sponsor

All Listed Sponsors
lead

ABL Bio, Inc.

INDUSTRY