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Terminated Phase 3 Interventional Results available

Double-blind, Randomized, Placebo-controlled Study Evaluating Efficacy and Safety of IgPro20 in Post-COVID-19 POTS

ClinicalTrials.gov ID: NCT06524739

Public ClinicalTrials.gov record NCT06524739. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 8:26 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Double-blind, Randomized, Placebo-controlled Phase 3 Study Evaluating Efficacy and Safety of IgPro20 (Subcutaneous Immunoglobulin, HIZENTRA®) in Post-COVID-19 Postural Orthostatic Tachycardia Syndrome (POTS)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a prospective, phase 3, multicenter, double-blind, randomized placebo-controlled study to investigate the efficacy, safety, and pharmacokinetics (PK) of repeat doses of IgPro20 in participants with post SARS-CoV-2 infection 2019 postural orthostatic tachycardia syndrome (post-Coronavirus Disease 2019 \[COVID-19\] POTS \[post-COVID-POTS\]).

Study identification

NCT ID
NCT06524739
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
CSL Behring
Industry
Enrollment
16 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 28, 2024 (Actual)
Primary completion
Jun 20, 2025 (Actual)
Completion
Jul 11, 2025 (Actual)
Last update posted
Apr 13, 2026

2024 – 2025

United States locations

U.S. sites
34
U.S. states
22
U.S. cities
32
Facility City State ZIP Site status
University of Alabama Hospital at Birmingham Birmingham Alabama 35294-1152 —
Center for Complex Neurology, EDS & POTS Phoenix Arizona 85006 —
Mayo Clinic Arizona Scottsdale Arizona 85259 —
Arkansas Cardiology Clinic - Little Rock Little Rock Arkansas 72205 —
UC San Diego Health La Jolla California 92037 —
University of california Irvine Orange California 92868 —
National Jewish Health Denver Colorado 80206 —
Hope Research Network Miami Florida 33166 —
Well Pharma Medical Research, Corp Miami Florida 33173 —
Velocity Clinical Research, Savannah Savannah Georgia 31406 —
LSU Health Sciences Center New Orleans Louisiana 70112 —
Velocity Clinical Research, Metairie New Orleans Louisiana 70119 —
Johns Hopkins Bayview Medical Center PMR Baltimore Maryland 21224 —
Mass General Brigham (Massachusetts General Hospital) Belmont Massachusetts 02478 —
Profound Research LLC at Millennium Affiliated Physicians Farmington Hills Michigan 48334 —
Velocity Clinical Research - Lincoln Lincoln Nebraska 68510 —
Dysautonomia Clinic Buffalo New York 14221 —
NYU Langone Health South Shore Neurologic Associates Patchogue New York 11772 —
Duke University Medical Center Durham North Carolina 27710 —
Bernstein Clinical Research Center Cincinnati Ohio 45236 —
University Hospital Cleveland Medical Center Cleveland Ohio 44195 —
Hightower Clinical Oklahoma City Oklahoma 73134 —
Penn Presbyterian Medical Center Philadelphia Pennsylvania 19104 —
Velocity Clinical Research - Union Union South Carolina 29379 —
Vanderbilt University Medical Center Nashville Tennessee 37232 —
UT Austin Dell Medical School Austin Texas 78712 —
University of Texas Southwestern Medical Center Dallas Texas 75390 —
Prolato Clinical Research Center Houston Texas 77054 —
Sunbeam Clinical Research McKinney Texas 75069 —
University of Texas Health Science Center San Antonio Texas 78229 —
Bateman Horne Center Salt Lake City Utah 84102 —
Metrodora Institute West Valley City Utah 84119 —
Velocity Clinical Research - Hampton Hampton Virginia 23666 —
VCU Health Richmond Virginia 23219 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06524739, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 13, 2026 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06524739 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →