drugset / Trial / NCT05462587

A Study to Evaluate Efficacy and Safety of AVTX-803 in Patients With Leukocyte Adhesion Deficiency Type II

NCT05462587 ↗

Phase 3 Recruiting 4 enrolled AUG Therapeutics
RandomizedCrossoverDouble-blindTreatment

Summary

The primary objective of this study is to evaluate the efficacy and safety of AVTX-803 compared to withdrawal in patients with Leukocyte Adhesion Deficiency, Type II (LAD II).

Timeline

Start
2022-07-28
Primary completion
2026-11-30
Completion
2026-11-30

Drugs

EvaluationDrugModalityDoseRoute
Subject AVTX-803 Unknown 1700 mg/kg —