drugset / Trial / NCT05756920

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

NCT05756920 ↗

Phase 1 Completed 91 enrolled ABL Bio, Inc.
RandomizedSequentialQuadruple-blindTreatment

Summary

This is a Phase 1, FIH, randomized, double-blind, placebo-controlled study designed to assess the safety, tolerability, PK and PD after SAD and MAD in healthy adult participants.

Timeline

Start
2022-12-31
Primary completion
2025-04-30
Completion
2025-04-30

Drugs

EvaluationDrugModalityDoseRoute
Subject ABL301 Unknown — Intravenous

Indications

No indication recorded.