Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06695741

Reduced Dose of Cyclophosphamide Combined With Standard Immunosuppressive Therapy to Treat Severe Aplastic Anemia

Reduced Dose of Cyclophosphamide Combined With Standard Immunosuppressive Therapy as Front-line Therapy in Patients With Severe Aplastic Anemia

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
75 (estimated)
Sponsor
Institute of Hematology & Blood Diseases Hospital, China · Academic / Other
Sex
All
Age
12 Years
Healthy volunteers
Not accepted

Summary

This is a prospective, single-center, single-arm, phase 2 study. This study aims to evaluate the efficacy and safety of anti-lymphocyte globulin plus herombopag in combination with the reduced dose of cyclophosphamide (hypo-CASH) for severe aplastic anemia.

Conditions

Interventions

TypeNameDescription
DRUGReduced dose of cyclophosphamide combined with standard immunosuppressive therapySevere aplastic anemia patients will receive a daily dose of Anti-lymphocyte globulin (25mg/kg) for the initial five days at the beginning of the treatment. Cyclosporine will be administered daily at a dosage of 3-5mg/kg. Herombopag will be administered daily at a dosage of 15mg starting from the first day of treatment and continuing for a duration of six months. Cyclophosphamide (20mg/kg) will be administered on days 15-16.

Timeline

Start date
2024-11-01
Primary completion
2027-02-01
Completion
2027-06-30
First posted
2024-11-19
Last updated
2024-11-19

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06695741. Inclusion in this directory is not an endorsement.