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
- Diseases
- Long COVID and ME/CFS
- 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
Sites (6)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Katholisches Klinikum Bochum gGmbH Coordinator of this site? Confirm its status | Bochum | Germany | Completed |
| Hospital Germans Trias i Pujol Coordinator of this site? Confirm its status | Badalona | Spain | Completed |
| Hospital Clinic de Barcelona Coordinator of this site? Confirm its status | Barcelona | Spain | Completed |
| Hospital Clínico San Carlos Coordinator of this site? Confirm its status | Madrid | Spain | Completed |
| Azienda Ospedaliero-Universitaria Policlinico Umberto I Coordinator of this site? Confirm its status | Rome | Italy | Completed |
| Humanitas Mirasole S.p.A. Coordinator of this site? Confirm its status | Rozzano | Italy | Completed |
This page is information, not medical advice. Discuss any trial with your doctor.