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Completed Phase 3 Interventional Results available

Avatrombopag for the Treatment of Thrombocytopenia in Pediatric Subjects With Immune Thrombocytopenia for ≥6 Months

ClinicalTrials.gov ID: NCT04516967

Public ClinicalTrials.gov record NCT04516967. 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 20, 2026, 4:03 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Randomized, Double-blind, Placebo-controlled Study With Open-label Extension Phase to Evaluate the Efficacy and Safety of Avatrombopag for the Treatment of Thrombocytopenia in Pediatric Subjects With Immune Thrombocytopenia for ≥6 Months

Brief summary

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

A Phase 3b Study to Evaluate the Efficacy and Safety of Avatrombopag for the Treatment of Thrombocytopenia in Pediatric Subjects with Immune Thrombocytopenia for ≥6 Months

Study identification

NCT ID
NCT04516967
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Sobi, Inc.
Industry
Enrollment
75 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
1 Year to 17 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
Mar 5, 2021 (Actual)
Primary completion
Nov 8, 2023 (Actual)
Completion
Oct 28, 2025 (Actual)
Last update posted
Jun 3, 2026

2021 – 2025

United States locations

U.S. sites
21
U.S. states
17
U.S. cities
21
Facility City State ZIP Site status
Site 112 Phoenix Arizona 85016 —
Site 103 Long Beach California 90806 —
Site 119 Orange California 92868 —
Site 109 Sacramento California 95817 —
Site 101 San Francisco California 94158 —
Site 111 Aurora Colorado 80045 —
Site 120 Wilmington Delaware 19803 —
Site 117 Gainesville Florida 32610 —
Site 116 Atlanta Georgia 30322 —
Site 107 Peoria Illinois 61615 —
Site 104 Boston Massachusetts 02115 —
Site 105 Minneapolis Minnesota 55404 —
Site 114 Jackson Mississippi 39216 —
Site 102 Las Vegas Nevada 89135 —
Site 108 Morristown New Jersey 07960 —
Site 118 Charlotte North Carolina 28203 —
Site 113 Durham North Carolina 27710 —
Site 106 Columbus Ohio 43205 —
Site 121 Philadelphia Pennsylvania 19104 —
Site 110 Providence Rhode Island 02903 —
Site 115 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 41 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04516967, 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 Jun 3, 2026 · Synced Oct 20, 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 NCT04516967 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →