drugset / Trial / NCT05920512

Combination Regimen With Sodium Valproate for Severe Hemophilia: a Single-arm, Phase 1, Pilot Trial.

NCT05920512

Phase 1/2 Unknown 10 enrolled Xue-chun Lu
NaSingle-groupOpen-labelTreatment

Summary

The goal of this clinical trial is to determine the clinical efficacy and toxic effects of sodium valproate, sirolimus and calcitriol in the treatment of severe haemophilia in participants with severe haemophilia . The main questions it aims to answer are the possibility of adding a combination regimen to primary treatment for severe haemophilia . Patients will receive oral sodium valproate extended-release tablets 0.5g/day, sirolimus tablets 1mg/day and osteopontin capsules 0.25μg/day.

Timeline

Start
2022-04-01
Primary completion
2025-04-01
Completion
2025-04-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Calcitriol Small molecule 0.25 ug
Subject Sirolimus Small molecule 1 mg Oral
Subject Valproate Small molecule 0.5 g Oral

Indications