drugset / Trial / NCT05835479

Rezafungin for Treatment of Pneumocystis Pneumonia in HIV Adults

NCT05835479

Phase 2 Recruiting 50 enrolled Mundipharma Research Limited
RandomizedParallel-groupOpen-labelTreatment

Summary

This study aims to generate clinical data on the efficacy, safety, and tolerability of rezafungin combined with 7 days of co-trimoxazole for treatment of Pneumocystis pneumonia (PCP) in adults living with human immunodeficiency virus (HIV), which would expand the knowledge of clinical use of rezafungin.

Timeline

Start
2023-11-14
Primary completion
2025-05
Completion
2025-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Rezafungin Other / unclassified 200 mg Intravenous
Comparator Sulfamethoxazole Small molecule 37.5 mg/kg Oral
Comparator Sulfamethoxazole Small molecule 50 mg/kg Oral
Comparator Sulfamethoxazole Small molecule 75 mg/kg Oral
Comparator Sulfamethoxazole Small molecule 100 mg/kg Oral
Comparator Trimethoprim Small molecule 7.5 mg/kg Oral
Comparator Trimethoprim Small molecule 10 mg/kg Oral
Comparator Trimethoprim Small molecule 15 mg/kg Oral
Comparator Trimethoprim Small molecule 20 mg/kg Oral

Indications