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NCT06524739CompletedPhase 3

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

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)

Source: EU CTIS (euclinicaltrials.eu) · Last updated 8 May 2025

Brief summary (registry, in English)

The primary objective of this study is to evaluate the efficacy of IgPro20 in comparison with placebo in adults with post-COVID POTS.

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
17 (actual)
First submitted
10 Jan 2025
Start date
1 Oct 2025
Lead sponsor
CSL Behring LLC
NCT number
NCT06524739
EU CT number
2023-508744-22-00

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 17
  • 6 sites in 3 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study, not your situation.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Treatment with Immunoglobulin G (IgG) or plasmapheresis within 12 weeks before Screening
  • Symptoms and / or diagnosis of or receiving treatment for POTS before COVID-19 infection
  • Prior diagnosis of or receiving current treatment at Screening for the following conditions (unless onset was related to the inciting POTS-associated COVID-19 infection): certain neurologic, autoimmune, endocrine, cardiac, or other disorders, and pre-existing psychiatric disorders.

Other illness

  • Presence of active infections, including human immunodeficiency virus infection, hepatitis B, hepatitis C, active SARS-CoV-2 infection, or any uncontrolled systemic infection

Who the study is looking for

  • Provide written informed consent and be willing and, in the opinion of the investigator, able to adhere to all protocol requirements.
  • Males and females aged ≥ 18 at the time of providing written informed consent.
  • Diagnosis of post-COVID POTS, defined by both a preceding COVID-19 infection based on confirmed historical documentation and onset of POTS symptoms developing within 4 months after COVID-19 infection as defined per consensus criteria.
  • COMPASS-31 score of at least 40 at the Screening visit.
  • Positive confirmatory standardized standing test (ie, HR increase of ≥ 30 bpm [≥ 40 bpm for participants aged 18 to 19 years] within 10 minutes in the absence of orthostatic hypotension) at the Screening visit.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (6)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Katholisches Klinikum Bochum gGmbH
Coordinator of this site? Confirm its status
BochumGermanyCompleted
Hospital Germans Trias i Pujol
Coordinator of this site? Confirm its status
BadalonaSpainCompleted
Hospital Clinic de Barcelona
Coordinator of this site? Confirm its status
BarcelonaSpainCompleted
Hospital Clínico San Carlos
Coordinator of this site? Confirm its status
MadridSpainCompleted
Azienda Ospedaliero-Universitaria Policlinico Umberto I
Coordinator of this site? Confirm its status
RomeItalyCompleted
Humanitas Mirasole S.p.A.
Coordinator of this site? Confirm its status
RozzanoItalyCompleted

This page is information, not medical advice. Discuss any trial with your doctor.