Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
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 Oct 22, 2026, 5:39 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 21, 2020 (Actual)
Primary completion
Sep 19, 2023 (Actual)
Completion
May 17, 2024 (Actual)
Last update posted
Sep 24, 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 24, 2024 · Synced Oct 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03866798 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →