drugset / Trial / NCT05345418

Umbilical Cord-Derived Mesenchymal Stem Cell (VCELL 1) for Male Patients With Sexual Deficiency

NCT05345418 ↗

RandomizedCrossoverOpen-labelOther

Summary

Sexual functional deficiency affects largely the physical conditions, life and sexual quality of the patients. Hypogonadism affects about 4 to 5 million men in the US, and the incidence increases with age. In our recent phase I clinical trial, we have shown that intravenous adipose - derived MSC administration was safe in female and male patients with hormone deficiency. Post-transplantation sexual satisfaction was observed in all patients enrolled in this study. Testosterone levels in males increased significantly after transplantation and were maintained at high levels for up to 6 months before decreasing again at the 12-month follow-up. The aim of this clinical trial was to assess the safety and effectiveness of allogeneic administration of MSCs in middle-aged people with sexual functional deficiency.

Timeline

Start
2022-04-01
Primary completion
2025-06-01
Completion
2025-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject umbilical cord-derived mesenchymal stem cell Cell therapy 1.5e+06 cells/kg Intravenous

Indications