drugset / Trial / NCT07035561

Rituximab Therapy in Patients With Treatment Refractory Hypersenstivity Pneumonitis

NCT07035561 ↗

Phase 2 Completed 30 enrolled Shereen Medhat Mohammed Elsayed Nassar
NaSingle-groupOpen-labelTreatment

Summary

Hypersensitivity pneumonitis (HP) presents with a highly variable clinical course, and Traditional treatment involves systemic corticosteroids in conjunction with strict avoidance of the offending antigen. However, a subset of patients with progressive disease remains unresponsive to conventional therapies. The objective of this study is to evaluate the therapeutic potential of Rituximab in individuals with refractory hypersensitivity pneumonitis who did not respond to conventional immunosuppressive therapy and antigen avoidance. Assessing FVC at three intervals: six months prior to the initiation of Rituximab therapy (M-6), at the time of treatment initiation (M0), and six months afterward (M+6).

Timeline

Start
2023-06-01
Primary completion
2025-01-31
Completion
2025-01-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Rituximab Monoclonal antibody 1 g Intravenous