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NCT05520892

Two Regimens of IVIG in the Treatment of Newly Diagnosed ITP in Children

Recruiting now Phase 4 Last updated 16 May 2024
What this trial tests

Phase 4 trial testing intravenous immunoglobulin in Newly Diagnosed Immune Thrombocytopenia in Children, First Line Treatment in 580 participants. Currently enrolling.

Timeline
6 October 2022
Primary endpoint
31 August 2025
31 August 2026

Quick facts

Lead sponsorFujian Medical University Union Hospital
PhasePhase 4
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment580
Start date6 October 2022
Primary completion31 August 2025
Estimated completion31 August 2026
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Fujian Medical University Union Hospital

Who can join

Adults 29 Days to 14, any sex, with Newly Diagnosed Immune Thrombocytopenia in Children, First Line Treatment. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To compare the efficacy of two different dosage regimens of intravenous immune globulin (IVIG) in the treatment of children with newly diagnosed immune thrombocytopenia, and to reduce related adverse reactions and economic burdens on the premise of ensuring the remission rate

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of intravenous immunoglobulin

Trials testing the same drug.

Other Fujian Medical University Union Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05520892.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing