Immune Thrombocytopenic Purpura (ITP) Clinical Trials

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Real-world Treatment Patterns and Outcomes of Eltrombopag in Patients With Primary Immune Thrombocytopenia

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

This study aims to describe the treatment patterns and clinical outcomes of treatment with eltrombopag in primary immune thrombocytopenia (ITP) patients treated with prior corticosteroid therapy. This study will use secondary data provided by health care professionals (HCPs) for a sample of primary ITP patients, and primary data from a structured HCP survey. Data will be collected from HCPs working in various clinical centers across the United States (US), United Kingdom (UK), and Germany.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 100
Healthy Volunteers: f
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⁃ HCP inclusion criteria:

• A licensed HCP (e.g., internal medicine specialist, hematologist, hematologist-oncologist or immunologist etc.) involved in the management of adult patients with primary ITP.

• Actively involved in treatment decision-making for primary ITP patients at the time of the study.

• Have a minimum of 3 years of experience managing patients with primary ITP.

• Currently, managing an average of at least 2 adult primary ITP patients per month, including those treated with eltrombopag.

• Able and willing to complete a web-based survey (approximately 60 to 70 minutes) and abstract data from 2 eligible patient charts.

• Practicing in one of the study countries (US, UK, or Germany).

• Have access to a computer or mobile device with internet connectivity to complete the survey.

• Not listed as inactive or retired in the panel database.

⁃ Patient-level inclusion criteria:

• Confirmed diagnosis of primary ITP.

• Aged ≥18 years at the time of diagnosis.

• Received first-line corticosteroid therapy (with or without intravenous immune globulin \[IVIg\]).

• Initiated eltrombopag treatment (with or without corticosteroids) as first non-steroidal ITP treatment between 01 January 2020 and 31 December 2024.

• Have at least 6 months of follow-up data available after the index date (unless deceased within that period).

Locations
Other Locations
Switzerland
Novartis
RECRUITING
Basel
Contact Information
Primary
Novartis Pharmaceuticals
novartis.email@novartis.com
+41613241111
Backup
Novartis Pharmaceuticals
Time Frame
Start Date: 2026-06-25
Estimated Completion Date: 2028-09-29
Participants
Target number of participants: 150
Treatments
Eltrombopag Cohort
Adult patients diagnosed with primary ITP who initiated eltrombopag treatment between 01 January 2020 and 31 December 2024 following corticosteroid treatment.
Sponsors
Leads: Novartis Pharmaceuticals

This content was sourced from clinicaltrials.gov