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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05920512
Study type Interventional
Source Chinese PLA General Hospital
Contact Xuechun Lu, M.D.
Phone 13241892863
Email luxuechun@126.com
Status Recruiting
Phase Phase 1/Phase 2
Start date April 1, 2022
Completion date April 1, 2025

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