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Safety and Efficacy of Levamisole Combined With Cyclosporine A in Patients With Subclinical Paroxysmal Nocturnal Hemoglobinuria and PNH in the Setting of Another Bone Marrow Failure Syndromes(PNH-2013)

Phase 2
Conditions
Paroxysmal Nocturnal Hemoglobinuria
Hemoglobinuria
Hemoglobinuria, Paroxysmal
Proteinuria
Urination Disorders
Thrombosis
Bone Marrow Failure
Aplastic Anemia,
Anemia, Hemolytic
Interventions
Drug: Levamisole+cyclosporin A+Glucocorticoids
Drug: Glucocorticoids
Registration Number
NCT01760096
Lead Sponsor
Institute of Hematology & Blood Diseases Hospital, China
Brief Summary

Paroxysmal nocturnal hemoglobinuria is an acquired chronic hemolytic anemia,this study is designed to evaluate the safety and efficacy of Levamisole combined with cyclosporine A in patients with Subclinical Paroxysmal Nocturnal Hemoglobinuria and PNH in the setting of another bone marrow failure syndromes

Detailed Description

Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal disorder of the hematopoietic stem cell characterized by intravascular hemolysis, hemoglobinuria, anemia, and thrombosis, Patients may be at high risk of thrombosis and may develop bone marrow failure or aplastic anemia, with low white blood cell and platelet counts,because the manifestation and pathologic processes are complicate,the treatment is very difficult,this study is designed to evaluate the safety and efficacy of Levamisole combined with cyclosporine A in patients with Subclinical Paroxysmal Nocturnal Hemoglobinuria and PNH in the setting of another bone marrow failure syndromes

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
50
Inclusion Criteria
  1. Clinical and biochemical signs of Subclinical Paroxysmal Nocturnal Hemoglobinuria and PNH in the setting of another bone marrow failure syndromes
  2. Diagnosis confirmed by Ham's test or Flow cytometry Patients have any Flow cytometry data
  3. patient should complete levamisole study for at least half a year
Exclusion Criteria
  1. Active infection which requires antibiotic treatment
  2. Pregnant or lactating women
  3. Epilepsy and mental illness
  4. Kidney and liver function abnormal

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Levamisole+cyclosporin A+GlucocorticoidsLevamisole+cyclosporin A+GlucocorticoidsLevamisole+cyclosporin A+Glucocorticoids
cyclosporin A+Glucocorticoidscyclosporin A+Glucocorticoidscyclosporin A+Glucocorticoids
GlucocorticoidsGlucocorticoidsGlucocorticoids
Primary Outcome Measures
NameTimeMethod
Number of patients in each group in complete or partial remission6 months

she got blood transfusion-independent,the hemoglobin became higher

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Institute of Hematology & Blood Diseases Hospital,

🇨🇳

Tianjin, Tianjin, China

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