RecruitingPhase 1NCT05189925

NADPH Oxidase Correction in mRNA-transfected Granulocyte-enriched Cells in Chronic Granulomatous Disease (CGD)

NADPH Oxidase Correction in mRNA Transfected Granulocyte-enriched Cells in Chronic Granulomatous Disease (CGD)


Sponsor

National Institute of Allergy and Infectious Diseases (NIAID)

Enrollment

25 participants

Start Date

Jul 22, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

Background: CGD is caused by a gene mutation. For people with CGD, their cells cannot kill germs well, so they can get frequent or life-threatening infections. Researchers want to see if a new procedure can help a person s cells kill germs for a short time. It uses messenger RNA (mRNA) to deliver correct instructions for the gene mutation to the cells. Objective: To test a procedure in which mRNA is added to a person s blood cells. Eligibility: Males aged 18-75 with CGD with a mutation in the gene that makes the protein gp91phox. Design: Participants will be screened with: Medical history Physical exam Blood and urine tests Swab to test for strep throat Some screening tests will be repeated during the study. Participants will be admitted to the NIH Clinical Center hospital for at least 7 days. They will have apheresis. For this, a medicine is injected under their skin to prepare their white blood cells for collection. An IV line is placed into an arm vein. Blood goes through the IV line into a machine that divides whole blood into red blood cells, plasma, and white blood cells. The white blood cells are removed, and the rest of the blood is returned to the participant through an IV line in their other arm. The next day, they will get their mRNA-corrected cells via IV. They will be monitored for 3 more days. After discharge, participants will keep a symptom diary. They will be contacted weekly for one month, and then once a month. They will have a follow-up visit 3 months after the infusion.


Eligibility

Sex: MALEMin Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a new approach to treat Chronic Granulomatous Disease (CGD), a rare inherited immune disorder where the body's infection-fighting cells cannot destroy certain bacteria and fungi. Researchers will use mRNA technology to temporarily 'fix' the immune cells (granulocytes) taken from the patient's blood and then infuse them back to fight infections. You may be eligible if: - You are a male aged 18 to 75 - You have a confirmed diagnosis of CGD (verified by DHR test and genetic or protein analysis) - You have a physician available at home for follow-up care - You are able to give informed consent You may NOT be eligible if: - You are currently unstable due to a severe acute infection - You have stage 4 chronic kidney disease or a very low kidney filtration rate - You have uncontrolled diabetes, severe heart failure, or serious liver problems - You have active hepatitis B, C, or HIV - You have a history of alcohol or drug abuse - You are female (this study is for males only) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BIOLOGICALgp91 Grans

Adults with gp91phox-deficient CGD without systemic infection will participate in a dose escalation trial to identify the MTD (the most effective yet safe dose) of gp91 Grans IV infusion.


Locations(1)

National Institutes of Health Clinical Center

Bethesda, Maryland, United States

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NCT05189925


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