Trial | NCT03164915  Report issue

Title

A Clinical Study to Evaluate the Efficacy and Safety of LIV-GAMMA SN Inj. in Primary Immune Thrombocytopenia (ITP)
A Multicenter, Open-Label, Phase III Study to Evaluate the Efficacy and Safety of LIV-GAMMA SN Inj. in Primary Immune Thrombocytopenia (ITP)

  • Phase

    Phase 3

  • Study Type

    Interventional

  • Status

    Completed No Results Posted

  • Study Participants

    37
The main purpose of this study is to assess the efficacy and safety of LIV-GAMMA SN Inj. in adult subjects with ITP. The primary objective of this study is to determine the responder rate. A response is defined as a platelet count of ≥30×10^9/L and at least a 2 fold increase of the baseline, confirmed on at least 2 separate occasions at least 7 days apart without bleeding. The secondary objectives are to evaluate the further efficacy assessments including duration of response, and the safety of LIV-GAMMA SN Inj.
Study Started
Oct 24
2016
Primary Completion
Apr 03
2018
Study Completion
Sep 28
2018
Last Update
Mar 30
2021

Biological LIV-GAMMA SN Inj.

LIV-GAMMA SN Inj. Experimental

Criteria 

Inclusion Criteria:

Diagnosis of ITP
Mean screening platelet count of <30×10^9/L from 3 qualifying platelet counts performed within 14 days before the start of treatment, with no individual platelet count above 35×10^9/L.
No other factors inducing ITP
Stable doses of ITP active treatment must not have modified the dose in the preceding 1 month and must maintain their prestudy dose during the study.

Exclusion Criteria:

Known for hypersensitivity reactions to blood products, intravenous immunoglobulin (IVIg) or immunoglobulin G
Immunoglobulin A (IgA) deficiency
Therapy with live attenuated virus vaccines 3 months before the first administration of LIV-GAMMA SN Inj.
Administration of other investigational product 1 month before the first administration of LIV-GAMMA SN Inj.
Administration of Rituximab 3 months before the first administration of LIV-GAMMA SN Inj.
Treatment with anti-coagulants, which may affect the function of platelet
Positive HIV, HBV, HCV
3-fold increase of ALT or AST compared to normal upper limit
eCFR < 30mL/min/1.73m^2
History of deep vein thrombosis (DVT) or IVIg-induced thrombotic compliances
Hemoglobin > 10g/dL
No Results Posted