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RECRUITING
NCT05754450
PHASE3

An Extension Study Assessing the Safety and Efficacy of AVTX-803 in Subjects With Leukocyte Adhesion Deficiency Type II

Sponsor: AUG Therapeutics

View on ClinicalTrials.gov

Summary

The primary objective of this extension study is to assess the long-term safety and efficacy of AVTX-803 in subjects with LAD II (SLC35C1-CDG).

Official title: A Phase 3, Open-Label, Extension Study to Assess the Long-term Safety and Efficacy of AVTX-803 in Subjects With Leukocyte Adhesion Deficiency Type II (LAD II)

Key Details

Gender

All

Age Range

6 Months - 75 Years

Study Type

INTERVENTIONAL

Enrollment

2

Start Date

2023-04-10

Completion Date

2026-12-31

Last Updated

2026-05-01

Healthy Volunteers

No

Interventions

DRUG

AVTX-803

L-fucose crystalline powder

Locations (1)

Mayo Clinic

Rochester, Minnesota, United States