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Completed Phase 4 Interventional Results available

Safety and Treatment Satisfaction in Adults With Chronic ITP After Switching to Avatrombopag From Eltrombopag or Romiplostim

ClinicalTrials.gov ID: NCT04638829

Public ClinicalTrials.gov record NCT04638829. 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 1, 2026, 9:59 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

Prospective, Multi-center, Open-label Study Measuring Safety and Treatment Satisfaction in Adult Subjects With Chronic Immune Thrombocytopenia (ITP) After Switching to Avatrombopag From Eltrombopag or Romiplostim

Brief summary

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

Evaluate the safety and tolerability of avatrombopag given for 90 days after stopping treatment with eltrombopag or romiplostim.

Study identification

NCT ID
NCT04638829
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Sobi, Inc.
Industry
Enrollment
60 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years 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
Mar 14, 2021
Primary completion
Jan 2, 2024
Completion
Jan 2, 2024
Last update posted
Jan 15, 2025

2021 – 2024

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
20
Facility City State ZIP Site status
Sobi Site 110 Tucson Arizona 85745
Sobi Site 119 Whittier California 90603
Sobi Site 123 Washington D.C. District of Columbia 20010
Sobi Site 129 Miami Florida 33143
Sobi Site 120 Ocala Florida 34474
Sobi Site 125 St. Petersburg Florida 33709
Sobi Site 118 Tampa Florida 33606
Sobi Site 126 Chicago Illinois 60612
Sobi Site 109 Peoria Illinois 61614
Sobi Site 124 New Orleans Louisiana 70112
Sobi Site 101 Bethesda Maryland 20817
Sobi Site 103 Lincoln Nebraska 68506
Sobi Site 121 Chapel Hill North Carolina 27514
Sobi Site 116 Greenville North Carolina 27834
Sobi Site 128 Cleveland Ohio 44106
Sobi Site 127 Philadelphia Pennsylvania 19104
Sobi Site 102 York Pennsylvania 17403
Sobi Site 104 Rock Hill South Carolina 29732
Sobi Site 113 Dallas Texas 75246
Sobi Site 108 Salt Lake City Utah 84132

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 NCT04638829, 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 15, 2025 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04638829 live on ClinicalTrials.gov.

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