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Not Yet RecruitingNCT06516484

Ropustin for Refractory Aplastic Anaemia After Radiotherapy - a Single-centre, Prospective, Open-label, Single-arm Study

Status
Not Yet Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
Peking Union Medical College Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

To investigate the efficacy and safety of roprostin in the treatment of refractory AA after radiotherapy.

Conditions

Interventions

TypeNameDescription
DRUGRomiplostimEnrolled patients were given roprostin (20 µg/kg subcutaneously once weekly) for at least 3 months, with discontinuation of roprostin for platelet counts ≥50 x 10\^9/L and continuation of roprostin for platelet counts \<50 x 10\^9/L. Responders were continued to 6 months. Responders continue to use the drug until 6 months.

Timeline

Start date
2024-07-30
Primary completion
2025-07-31
Completion
2025-12-31
First posted
2024-07-24
Last updated
2024-07-24

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06516484. Inclusion in this directory is not an endorsement.

Ropustin for Refractory Aplastic Anaemia After Radiotherapy - a Single-centre, Prospective, Open-label, Single-arm Study (NCT06516484) · Clinical Trials Directory