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Terminated Phase 4 Interventional Results available

Study to Evaluate the Efficacy and Safety of PANZYGA in Pediatric Patients With Chronic Immune Thrombocytopenia (ITP)

ClinicalTrials.gov ID: NCT03866798

Public ClinicalTrials.gov record NCT03866798. 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 Sep 6, 2026, 6:46 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

Post-Marketing Study to Evaluate the Efficacy and Safety of PANZYGA in Pediatric Patients With Chronic Immune Thrombocytopenia (ITP)

Brief summary

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

This is a prospective, open-label, single-arm, multicenter, Phase 4 study evaluating the efficacy and safety of PANZYGA in pediatric patients with chronic ITP.

Study identification

NCT ID
NCT03866798
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Lead sponsor
Octapharma
Industry
Enrollment
6 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
1 Year to 18 Years
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
Jan 20, 2020
Primary completion
Sep 18, 2023
Completion
May 16, 2024
Last update posted
Sep 23, 2024

2020 – 2024

United States locations

U.S. sites
8
U.S. states
6
U.S. cities
8
Facility City State ZIP Site status
Octapharma Research Site Sacramento California 95817
Octapharma Research Site Minneapolis Minnesota 55404
Octapharma Research Site Rochester Minnesota 55905
Octapharma Research Site Columbus Ohio 43205
Octapharma Research Site Toledo Ohio 43606
Octapharma Research Site Philadelphia Pennsylvania 19104
Octapharma Research Site Providence Rhode Island 02903
Octapharma Research Site Houston Texas 77030

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03866798, 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 Sep 23, 2024 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03866798 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →