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Immunomodulatory Agent

IVIG for POTS (iSTAND Trial)

Phase 1 & 2
Waitlist Available
Led By Steven Vernino, MD, PhD
Research Sponsored by University of Texas Southwestern Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Confirmed personal history or family history of defined autoimmune disease including Hashimoto's thyroiditis, celiac disease, antiphospholipid syndrome, rheumatoid arthritis, SLE, or Sjogren's syndrome
One or more serum autoantibodies (ANA ≥ 1:160, gAChR antibody > 0.2 nmol/L, positive ENA, aPL, TTG, gliadin) or inflammatory markers (ESR > 30, CRP > 2, low C3 complement or low immunoglobulin IgG level)
Must not have
Inadequate peripheral venous access
Current or previous immunosuppression therapy or IVIG treatment
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 weeks
Awards & highlights

Summary

This trial aims to see if IVIG can help people with POTS who have autoimmune issues. IVIG is a treatment made from donated blood that gives extra antibodies to help control the immune system. The study will test if this treatment can improve symptoms in these patients. IVIG has been used for over two decades to treat various autoimmune and systemic inflammatory diseases.

Who is the study for?
This trial is for adults with POTS who have moderate to severe autonomic symptoms and signs of autoimmunity, such as certain autoantibodies or a personal/family history of autoimmune diseases. Participants must be stable on current medications and able to walk. Pregnant or breastfeeding women, those with poor vein access, previous immunosuppression therapy or IVIG treatment, allergies to blood products, kidney/liver disease, recent thrombosis, or other major medical issues are excluded.
What is being tested?
The study tests if IVIG (Gamunex-C), an immune-modulating treatment, can relieve symptoms in POTS patients showing signs of autoimmunity. It compares the effects of IVIG against Albumin (a plasma protein solution) in improving patient conditions.
What are the potential side effects?
IVIG may cause side effects like headaches including migraine-like pain after infusion (aseptic meningitis), allergic reactions including skin rashes and breathing difficulties, potential hemolysis (breakdown of red blood cells), and possible kidney function impact.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I or someone in my family has an autoimmune disease like Hashimoto's, celiac, or rheumatoid arthritis.
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I have high levels of certain antibodies or markers indicating inflammation.
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I can walk by myself at the time of screening.
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I experience moderate to severe symptoms related to my body's automatic functions.
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I have been diagnosed with POTS.
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I have swallowing or digestion problems that have caused me to lose weight.
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My oral medication has not changed in the last 3 months.
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I am 18 or older and can give my consent.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I have poor vein access for IVs.
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I am currently on or have had immunosuppression therapy or IVIG treatment.
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I am a premenopausal woman who is either pregnant or breastfeeding.
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My kidney or liver function tests are abnormal.
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I cannot receive treatments through IV that include immunoglobulin or albumin.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and 12 weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Improvement in symptoms measured by change in COMPASS-31 score.

Trial Design

2Treatment groups
Active Control
Placebo Group
Group I: Treatment IVIG ArmActive Control1 Intervention
IVIG (Gammunex-C) infusion (0.4 gm/kg) every week for 4 weeks, then every 2 weeks for 8 weeks (12 weeks total).
Group II: Treatment Albumin ArmPlacebo Group1 Intervention
albumin infusion (0.4 gm/kg) every week for 4 weeks then every 2 weeks for 8 weeks (12 weeks total) during

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for Postural Orthostatic Tachycardia Syndrome (POTS) include medications like beta-blockers, fludrocortisone, and midodrine, which help manage heart rate and blood pressure. Beta-blockers reduce heart rate and improve symptoms by blocking the effects of adrenaline. Fludrocortisone increases blood volume by promoting sodium retention, which helps prevent blood pressure drops upon standing. Midodrine constricts blood vessels, increasing blood pressure and reducing symptoms of dizziness and fainting. Immunomodulatory treatments like IVIG are being studied for their potential to modulate the immune system, which may be beneficial for POTS patients with autoimmune components. These treatments are crucial as they address the underlying mechanisms causing POTS symptoms, thereby improving patients' quality of life.

Find a Location

Who is running the clinical trial?

Grifols Biologicals, LLCIndustry Sponsor
32 Previous Clinical Trials
9,426 Total Patients Enrolled
Dysautonomia InternationalOTHER
5 Previous Clinical Trials
389 Total Patients Enrolled
5 Trials studying Postural Orthostatic Tachycardia Syndrome
389 Patients Enrolled for Postural Orthostatic Tachycardia Syndrome
University of Texas Southwestern Medical CenterLead Sponsor
1,072 Previous Clinical Trials
1,056,232 Total Patients Enrolled
1 Trials studying Postural Orthostatic Tachycardia Syndrome
350 Patients Enrolled for Postural Orthostatic Tachycardia Syndrome

Media Library

IVIG (Immunomodulatory Agent) Clinical Trial Eligibility Overview. Trial Name: NCT03919773 — Phase 1 & 2
Postural Orthostatic Tachycardia Syndrome Research Study Groups: Treatment IVIG Arm, Treatment Albumin Arm
Postural Orthostatic Tachycardia Syndrome Clinical Trial 2023: IVIG Highlights & Side Effects. Trial Name: NCT03919773 — Phase 1 & 2
IVIG (Immunomodulatory Agent) 2023 Treatment Timeline for Medical Study. Trial Name: NCT03919773 — Phase 1 & 2
~4 spots leftby Sep 2025