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Completed Phase 3 Interventional Results available

A Study Evaluating the Safety and Efficacy of Long-term Dosing of Romiplostim in Thrombocytopenic Pediatric Patients With Immune (Idiopathic) Thrombocytopenia Purpura

ClinicalTrials.gov ID: NCT01071954

Public ClinicalTrials.gov record NCT01071954. 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 Jul 22, 2026, 11:15 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

An Open Label Study Evaluating the Safety and Efficacy of Long-term Dosing of Romiplostim in Thrombocytopenic Pediatric Subjects With Immune (Idiopathic) Thrombocytopenia Purpura (ITP)

Study identification

NCT ID
NCT01071954
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Amgen
Industry
Enrollment
66 participants

Conditions and interventions

Eligibility (public fields only)

Age range
1 Year and older
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
Dec 29, 2009
Primary completion
Jan 11, 2017
Completion
Jan 11, 2017
Last update posted
Jan 17, 2020

2009 – 2017

United States locations

U.S. sites
24
U.S. states
18
U.S. cities
23
Facility City State ZIP Site status
Research Site Orange California 92868
Research Site San Diego California 92123
Research Site Washington D.C. District of Columbia 20010
Research Site Atlanta Georgia 30322
Research Site Chicago Illinois 60611
Research Site Peoria Illinois 61615
Research Site Indianapolis Indiana 46260
Research Site Iowa City Iowa 52242
Research Site Louisville Kentucky 40202
Research Site New Orleans Louisiana 70118
Research Site Detroit Michigan 48201
Research Site Kansas City Missouri 64108
Research Site Omaha Nebraska 68114
Research Site Las Vegas Nevada 89109
Research Site New Brunswick New Jersey 08901
Research Site New York New York 10016
Research Site New York New York 10021
Research Site Cincinnati Ohio 45229
Research Site Columbus Ohio 43205
Research Site Pittsburgh Pennsylvania 15224
Research Site Nashville Tennessee 37232
Research Site Dallas Texas 75390
Research Site Fort Worth Texas 76104
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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01071954, 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 Jan 17, 2020 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01071954 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →