drugset / Trial / NCT03700229

Study to Evaluate Rituximab and Bortezomib in Patients With Newly Diagnosed Acquired Hemophilia A

NCT03700229 ↗

Phase 2 Unknown 22 enrolled Peking Union Medical College Hospital
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this prospective study is to determine the efficacy and safety of Rituximab plus Bortezomib in patients with newly diagnosed acquired hemophilia A.

Timeline

Start
2018-10-10
Primary completion
2019-10-15
Completion
2020-04-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Bortezomib Small molecule 1.3 mg/m2 Intravenous
Subject Rituximab Monoclonal antibody 375 mg/m2 Intravenous
Subject Rituximab Monoclonal antibody 500 mg Intravenous

Indications