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A Clinical Study to Evaluate the Efficacy and Safety of LIV-GAMMA SN Inj. in Primary Immune Thrombocytopenia (ITP)

S

SK Plasma

Status and phase

Completed
Phase 3

Conditions

Immune Thrombocytopenia

Treatments

Biological: LIV-GAMMA SN Inj.

Study type

Interventional

Funder types

Industry

Identifiers

NCT03164915
IVIg_ITP_III_2016

Details and patient eligibility

About

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.

Enrollment

37 patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

37 participants in 1 patient group

LIV-GAMMA SN Inj.
Experimental group
Treatment:
Biological: LIV-GAMMA SN Inj.

Trial contacts and locations

6

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Data sourced from clinicaltrials.gov

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