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

Terminated · Phase 3 · NCT06524739

Conditions: Post-COVID Postural Orthostatic Tachycardia Syndrome

At a glance

Research payments reported, 2025
$4.1M
U.S. investigators named
25
Sites paid
21
Planned or actual enrollment
16

About the trial

Sponsor
CSL Behring
Tested
IgPro20 (biological), Placebo (biological)
Dates
Started 2024-08-28; completion 2025-07-11
Results posted
Yes

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 \[post-COVID-POTS\]).

From ClinicalTrials.gov, last updated 2026-04-13. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Csl Behring reported $4.1M in research payments for this study in 2025 (499 payments).

Products named: Hizentra

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.