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NCT05462587 · ClinicalTrials.gov registry record · Phase 3
A Study to Evaluate Efficacy and Safety of AVTX-803 in Patients with Leukocyte Adhesion Deficiency Type II
A Phase 3 study of Leukocyte Adhesion Deficiency, sponsored by AUG Therapeutics.
- Recruiting
- Registry status
- Phase 3
- Development phase
- 4
- Enrollment target
- 1
- Study location
NCT05462587: Recruiting Phase 3 study of Leukocyte Adhesion Deficiency, sponsored by AUG Therapeutics.
NCT05462587 is a Phase 3 study of Leukocyte Adhesion Deficiency that is actively recruiting participants, run by AUG Therapeutics. The registered enrollment target is 4 participants. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05462587, a Phase 3 study of Leukocyte Adhesion Deficiency, is actively recruiting participants, sponsored by AUG Therapeutics.
- RECRUITING
- Registry status
- Phase 3
- Development phase
- 4 participants
- Enrollment target
- 1
- Study location
Study 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).
Conditions Studied
Interventions
- DRUG AVTX-803 (L-Fucose)
Study Locations (1)
Minnesota
- Mayo Clinic - Rochester
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 4 participants |
| Start Date | 2022-07-28 |
| Est. Completion | 2024-11-30 |
| Phase | Phase 3 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05462587
The ClinicalTrials.gov registry entry for NCT05462587 describes a study currently listed as recruiting, categorized as Phase 3. The registered enrollment target is 4 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AUG Therapeutics, which has 2 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Leukocyte Adhesion Deficiency appearing as the primary indexed condition, and to 1 intervention - of which AVTX-803 (L-Fucose) is the first listed.
NCT05462587 reports 1 study location spanning 1 distinct geographic area - top geographies include Minnesota.
Frequently Asked Questions
What is clinical trial NCT05462587 about?
NCT05462587 is a clinical study titled "A Study to Evaluate Efficacy and Safety of AVTX-803 in Patients with Leukocyte Adhesion Deficiency Type II". 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).
What is the current status of trial NCT05462587?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 4 participants. The study started on 2022-07-28. Estimated completion is 2024-11-30.
What conditions does trial NCT05462587 study?
This clinical trial studies the following conditions: Leukocyte Adhesion Deficiency.
What interventions are being tested in trial NCT05462587?
The interventions under investigation include: AVTX-803 (L-Fucose) (DRUG).
Who is sponsoring clinical trial NCT05462587?
This trial is sponsored by AUG Therapeutics, which has 2 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05462587 being conducted?
This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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